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<h3>Job Description</h3>
Job Description
Who We Are
Quality Work. Quality Results.
Bay West stands at the forefront of the environmental consulting and remediation sector. Our dedication to safety, innovation, and our skilled team has driven us for over fifty years, delivering top-tier environmental consulting, industrial, and emergency response services. At Bay West, you'll be driven to innovate and make a real impact on environmental issues, all while advancing your career in a dynamic and supportive environment.
This Opportunity
We are seeking a motivated and detail-oriented Geologist I to join Bay West. You’ll conduct environmental sampling, assist with a range of field projects, support emergency response efforts, and gain hands-on experience. This role is a great opportunity to make a real impact on environmental work while growing your skills and advancing your career!
Your Key Responsibilities
<ul>
<li>Conduct field work as requested, to include out-of-town travel for up to two weeks at a time, multiple times a year</li>
<li>Read/understand SOPs and obtain training on specific field tasks required</li>
<li>Accurately and efficiently conduct environmental sampling (air, water, soil, sediment) in accordance with the supplied work plan and SOPs with minimal oversight</li>
<li>Assist Site Supervisor in various highway construction projects as well as conducting roadway preconstruction investigations</li>
<li>Assist in the correct installation of soil borings, monitoring wells, recovery wells (vapor phase and water) and treatment systems.</li>
<li>Accurately and efficiently log soil cores/cuttings and prepare geologic boring logs and descriptions under supervisor of a Site Supervisor.</li>
<li>Oversee the proper excavation of contaminated soil during remediation and construction projects under supervision of a Site Supervisor.</li>
<li>Organize, digitize and file field notes in Document Locator in a timely manner</li>
<li>Utilize and maintain field equipment in accordance with Bay West SOPs</li>
<li>Help resolve problems as they arise in the field</li>
<li>Manage schedule and relationships to maintain utilization goals and complete activities within promised time frames</li>
<li>Demonstrate competency with most field activities, including various methods of drilling, soil, and groundwater sampling</li>
<li>Assist in overseeing drilling and excavation crews, including conducting health and safety tailgate meetings and directing field crews</li>
<li>Enter field and laboratory data
<ul>
<li>Requires Excel skills</li>
<li>Attention to detail is critical</li>
<li>Summarize field methods and results</li>
</ul>
</li>
<li>Technical services - Geology/hydrogeologic analysis
<ul>
<li>Help prepare well log summaries</li>
</ul>
</li>
<li>When not traveling, be available for one week out of every eight weeks to be part of an on-call Emergency Response (ER) team to clean-up hazardous and non-hazardous material spills, loading, unloading, and decontaminating ER equipment in an efficient and accurate manner </li>
<li>Ability to travel 25 - 30%. </li>
</ul>
Who You Are
Required Qualifications
<ul>
<li>BS - Geology, Earth Sciences, or Related (must meet education requirements to obtain professional geologist licensure)</li>
<li>1 to 3 years of environmental experience in similar role</li>
<li>Current 40-hour HAZWOPER certification or ability to obtain within 30 days </li>
<li>Able to obtain site access to secure areas such as Federal or State sites </li>
<li>Ability to employ common field practices involving drilling, groundwater sampling, and excavation oversight</li>
<li>Ability to read and understand maps, schematic drawings, diagrams, and instruction manuals</li>
<li>Proficiency using Word and Excel applications</li>
<li>Must have a valid driver’s license. </li>
<li>Experience with field equipment such as water quality monitoring instruments, photoionization detectors (PIDs), and global positioning systems (GPS) units</li>
</ul>
Physical Requirements
<ul>
<li>Ability to function in work environments that sometimes include high heat; high humidity; extreme cold; roadway traffic hazards; on water (boat operations) and confined spaces.</li>
<li>Adequate vision and hearing to safely see teammates hand signals and hear warning communication in low light.</li>
<li>Substantial repetitive movements of the wrists, hands and/or fingers (including reaching, grasping, twisting, pushing, and pulling).</li>
<li>Walking on uneven surfaces &amp; climbing stairs/ladders.</li>
<li>Semi-frequent crouching, bending, stooping and twisting, occasionally in tight spaces.</li>
<li>Sitting in a vehicle for up to eleven hours straight.</li>
<li>Working while standing during a 12-hour workday.</li>
<li>Frequently lifting up to 10 lbs. over an 8-hour period and occasionally up to 50 lbs. over a four-hour period.</li>
<li>Occasionally lifting 3-6” diameter hoses that weigh approximately 20 pounds over the head onto hose racks.</li>
<li>Managing a 55-gallon drum containing approximately 400 pounds of material onto a drum dolly, then moving the drum using the dolly.</li>
</ul>
Benefits
Bay West offers a comprehensive benefits package available to eligible employees, including but not limited to paid time off, health insurance options, ancillary benefits to support life at all stages, 401(k), employee assistance programs, and subsidies.

Geologist I

<h3>Job Description</h3>
NYU Langone Health is a fully integrated health system that consistently achieves the best patient outcomes through a rigorous focus on quality that has resulted in some of the lowest mortality rates in the nation. Vizient Inc. has ranked NYU Langone the No. 1 comprehensive academic medical center in the country for three years in a row, and U.S. News &amp; World Report recently placed nine of its clinical specialties among the top five in the nation. NYU Langone offers a comprehensive range of medical services with one high standard of care across 6 inpatient locations, its Perlmutter Cancer Center, and over 320 outpatient locations in the New York area and Florida. With $14.2 billion in revenue this year, the system also includes two tuition-free medical schools, in Manhattan and on Long Island, and a vast research enterprise with over $1 billion in active awards from the National Institutes of Health. For more information, go to NYU Langone Health, and interact with us on LinkedIn, Glassdoor, Indeed, Facebook, Twitter, YouTube and Instagram.
Position Summary: We have an exciting opportunity to join our team as a Physicist - Radiation Oncology (Staten Island + float to other campuses). In this role, the successful candidate will be responsible for maintenance of quality assurance program, supervision and review of dosimetrists tasks, review of planning procedures and oversight of the patient planning and treatment process with brachytherapy or external beam radiation therapy
Job Responsibilities:
<ul>
<li>Treatment Planning: Identifies and evaluates target volumes and critical structures. Generates QA plans as required for IMRT and reference points as needed for physics checks. Follows established policies and procedures as they relate to treatment planning. Demonstrated level of planning capability. Completeness of RT electronic charts: setup fields, DRR, CBCT, ref points, scheduling.</li>
<li>Performs other duties as assigned.</li>
<li>Quality Assurance: Performs assigned quality assurance tasks in a complete and timely fashion (linac monthly and annual QA, IMRT QA, brachytherapy QA). Performs assigned quality assurance tasks in a complete and timely fashion (initial chart checks, weekly chart checks, final chart review). Documents all quality assurance work in a complete and timely fashion and determines compliance in all categories included in the lists; initiates corrective action when necessary.</li>
<li>Participates in in-service programs and conferences. Attends all required department in-service meetings. Attends annual billing/documentation/safety classes. Attends annual Radiation Safety in-service.</li>
<li>Participation in training of Residents and Students: Assists in the training of Residents and Students on use of Eclipse or ARIA and the principle of treatment planning. Participates in research protocols.</li>
<li>Initiative: Makes suggestions for positive changes. Demonstrates ability to understand tasks and creatively apply solutions. Demonstrates ability to adopt and help develop new physics initiatives and policies. Readily accepts new assignments and responsibilities. Recognizes when help is needed by others and offers guidance and assistance. Monitors patient tracker to effect a smooth and orderly process for patients and staff.</li>
<li>Planning and Time Utilization: Work is thought out and planned in advance and successfully implemented. Coordinates own work to achieve efficiency and quality patient care. Work is completed in a timely manner, meeting schedules.</li>
<li>Documentation: All paperwork and electronic forms are complete, signed and labeled accordingly. Procedure codes are complete, timely and accurate. Documents, dates &amp; signs all changes to treatment set-up. Documentation for clinical trials and protocols is coordinated with appropriate parties.</li>
</ul>
Minimum Qualifications: To qualify you must have a Master's of Science degree in physics or engineering and completion of a training/residency program or a Master's Degree in an accredited Medical Physics program. Required license NYS Med Physicist License (Grace period - NA) or NYS Limited Med Physicist Permit (Grace period - NA) Well developed communication and computer skills. Required Licenses: NYS Limited Med Physicist Perm, NYS Med Physicist License
Preferred Qualifications: Certification (ABR);
Qualified candidates must be able to effectively communicate with all levels of the organization. NYU Langone Health provides its staff with far more than just a place to work. Rather, we are an institution you can be proud of, an institution where you'll feel good about devoting your time and your talents.
At NYU Langone Health, we are committed to supporting our workforce and their loved ones with a comprehensive benefits and wellness package. Our offerings provide a robust support system for any stage of life, whether it's developing your career, starting a family, or saving for retirement. The support employees receive goes beyond a standard benefit offering, where employees have access to financial security benefits, a generous time-off program and employee resources groups for peer support. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care. The benefits and wellness package is designed to allow you to focus on what truly matters. Join us and experience the extensive resources and services designed to enhance your overall quality of life for you and your family. NYU Langone Health is an equal opportunity employer and committed to inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration. We require applications to be completed online.
View Know Your Rights: Workplace discrimination is illegal.
NYU Langone Health provides a salary range to comply with the New York state Law on Salary Transparency in Job Advertisements. The salary range for the role is $213,477.55 - $235,000.00 Annually. Actual salaries depend on a variety of factors, including experience, specialty, education, and hospital need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.
To view the Pay Transparency Notice, please click here

Physicist - Radiation Oncology (Staten Island + float to other campuses)

<h3>Job Description</h3>
Job Description
Job Summary:
As a critical member of our technology team, Lead Chemists coordinate with Senior Management to oversee day-to-day lab activities conducted by the lab technicians, perform research and develop projects, oversee or perform quality control, provide technical support to the JAX Sales Team and customers, and continue to improve existing products, formulas, processes, and equipment.

Duties and Responsibilities: 
<ul>
<li>Facilitate and lead all lab testing for quality control, raw material qualification, project and technical support requests</li>
<li>Provide batch fixes to out-of-spec products</li>
<li>Serve as project lead in the lab, including
<ol>
<li>Development of project layouts</li>
<li>Work with the VP of Technology, Sales Team, Marketing, and end-users to further define project needs</li>
<li>Identify testing needs</li>
<li>Determine when project results meet product needs</li>
<li>Present project findings and results to the VP of Technology</li>
<li>Set up and oversee field trials</li>
</ol>
</li>
<li>Generate technical reports based on research and development projects or technical service requests</li>
<li>Work with JAX Sales Team and customers to interpret the technical reports, test results, and recommendations</li>
<li>Research new technologies including chemicals, applications, and equipment by working with raw material suppliers, equipment manufacturers or online resources</li>
<li>Present ideas for formulation improvements to VP of Technology</li>
<li>Provide JAX product recommendations based on application or product cross references to competitive products</li>
<li>As the reactive technical representative, provide field support by troubleshooting at the customer level, identifying application needs and technical support</li>
<li>Serve as primary contact for outside ISO audits and FM Global</li>
<li>Participate in and contribute to internal ISO audits</li>
<li>Work with the VP of Technology to develop lab policies, work instructions, forms and testing protocols</li>
<li>Provide leadership to Lab Technicians and Chemists including: time and task management, development of professional skills and continuing education, testing, applications, and formulations</li>
<li>Minimal travel as required</li>
<li>Other duties as assigned</li>
</ul>
 
Required Skills and Abilities:
<ul>
<li>Ability to observe, research and interpret a subject, data, or problem to develop complex ideas and solutions</li>
<li>Excellent time management and organizational skills</li>
<li>Effective communication skills</li>
</ul>

Education and Experience:
<ul>
<li>Bachelor of Science in Chemistry or related field of study.</li>
<li>2-5 years of laboratory experience is preferred</li>
</ul>

Equipment Used:
General lab testing equipment for quality control and research and development. Equipment may include:
<ul>
<li>FTIR</li>
<li>GC-MS</li>
<li>ICP</li>
<li>Kinematic Viscosity</li>
<li>UV-VIS</li>
<li>TGA</li>
</ul>

Lead Chemist

<h3>Job Description</h3>
Job DescriptionRole Summary
<ul>
<li>Responsibilities: You will be responsible for devising and performing statistical analysis plans and then communicating the methodologies and results of these to our clients in the healthcare sector</li>
<li>Salary: $73,000 to $76,000 depending on qualifications and previous experience</li>
<li>Benefits: Discretionary profit share bonuses paid twice per year, hybrid and flexible working options, generous vacation allowance, private medical and dental insurance, 401K plan with up to a 5% employer contribution, life insurance, full funding and study leave for external training and more</li>
<li>Role Type: Full-time, permanent </li>
<li>Start Date: We are currently recruiting for start dates in early 2026 and you will be asked to state your availability on your application form</li>
<li>Application Deadlines: Whilst there are no set application deadlines, we strongly recommend applying as early as possible. The role, or particular start dates, may close when suitable candidates are found</li>
<li>Location: This role is available in our Boston office </li>
</ul>
About the Role
Our Statistics team provide statistical and analytical expertise across Costello Medical, devising statistical analysis plans and performing data analysis within R, Excel, Stan, SQL and BUGS software. They are also responsible for communicating the methodologies and results in both written and oral formats to drug and device manufacturers, and doctors. The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic statistical analysis of individual patient data, regression analysis, survival analysis and complex Bayesian network meta-analysis using both standard and emerging methods.
You will work in project teams alongside colleagues from all specialities to ensure that statistics projects are completed to an exceptionally high standard, on time and in line with client expectations. You will receive training in the technical aspects of the role, project management skills and effective client communication. Delivering project work requires close collaboration with clients and, following a successful induction period, you will increasingly participate in client calls and face-to-face meetings with external stakeholders. 
Our team typically work on several projects at one time and the results of each analysis can feed into publications, value materials, health economic models or health technology assessment submissions. You will therefore be exposed to a wide variety of our services and a broad range of therapeutic areas. To read more about our recent articles and publications, please visit our website: <a href="https://www.costellomedical.com/research/articles-publications/" target="_blank">https://www.costellomedical.com/research/articles-publications/</a>
Hybrid Working Policy: We believe that having face-to-face time in the office holds many benefits and is central to ensuring that the community we have created, where people have a workplace they belong to and feel part of, is never lost. At the same time, we recognize that homeworking can improve work life balance, reduce commuting times and costs, and provide the opportunity to juggle personal commitments. Therefore, we offer flexible working arrangements that allow our colleagues to work from home for up to half of the time, measured across a 2-week rolling period. Please note that as part of our wider flexible working policy, employees may work outside of Massachusetts for up to 4 weeks annually
A Day in the Life of a Statistician
To learn more about a typical day for a Statistician at Costello Medical, please click here: <a href="https://www.costellomedical.com/day-in-the-life/statistician.html" target="_blank">https://www.costellomedical.com/day-in-the-life/statistician.html</a>
Career Profile
We offer many opportunities for personal and professional development at Costello Medical. Please click below to read firsthand accounts from our colleagues about their time with the company: <a href="https://www.costellomedical.com/careers/working-at-costello-medical/" target="_blank">https://www.costellomedical.com/careers/working-at-costello-medical/</a>
About Costello Medical
Costello Medical is a rapidly growing global healthcare agency specializing in medical communications, market access and health economic and outcomes research. We work with a wide range of clients, including the industry’s most successful pharmaceutical and medical technology companies, patient and public health bodies and charitable organizations. We have been listed in the Top 100 Best Companies to Work For list since 2017, the Boston Globe’s Top Places to Work list in 2025, and were proud to receive B Corporation accreditation in 2022. Please click here to learn more about us, our work and our mission: <a href="https://www.costellomedical.com/" target="_blank">https://www.costellomedical.com/</a>
Requirements
About You
The successful candidate will be someone who enjoys problem solving and thinking outside the box to develop innovative solutions. In line with the company’s values, you will be passionate about improving patient outcomes by applying your statistical knowledge and technical skills to the healthcare industry.
Essentialrequirements for the role are:
<ul>
<li>A degree level or higher qualification in a scientific or mathematical discipline (minimum GPA 3.3) with a focus on statistics and data analysis. </li>
<li>Proficiency in the R programming language, and the willingness and ability to rapidly develop your programming skills</li>
<li>The technical and mathematical ability, coupled with the written and oral communication skills, to explain complex techniques and results to non-experts</li>
<li>A willingness to trial, explore or recommend new software or techniques that may suit specific projects</li>
<li>A high degree of accuracy and attention to detail, along with the ability to maintain a high level of customer service and the quality of deliverables under multiple competing demands</li>
<li>A high level of organisation, with the flexibility to respond to changing deadlines</li>
<li>The ability to use your initiative and work independently, in addition to working collaboratively within project teams</li>
<li>Excellent written English, which will be assessed during the selection process</li>
</ul>
Desired requirements for the role are:
<ul>
<li>A Masters degree or PhD in a scientific or mathematical discipline </li>
<li>Experience with Python Stan, SQL</li>
<li>Experience in and/or knowledge of medical data, clinical processes or trials</li>
</ul>
Joining Costello Medical from Academia
At Costello Medical, we warmly welcome applicants from academia who are looking to transitioning into a role within a commercial, industry-based setting. We understand the unique perspectives and valuable skills that academic professionals bring to our team. To support your career change, we offer comprehensive training, mentorship programs, and a work culture that fosters collaboration, growth and innovation. We are committed to facilitating a smooth transition and helping you thrive in an industry-based setting.
Many of our team members have successfully made this transition, and they share how their expertise has been transformed into fulfilling, impactful careers with us. Learn more here: <a href="https://www.costellomedical.com/careers/working-at-costello-medical/joining-from-academia/" target="_blank">https://www.costellomedical.com/careers/working-at-costello-medical/joi…</a>
Benefits
What We Offer
Alongside our award-winning company culture, where every team member is celebrated, respected, and has their voice heard, our comprehensive benefits package includes:
<ul>
<li>A starting salary of $73,000 to $76,000 per annum, depending on your qualifications and previous experience, as well as a discretionary profit share bonus paid twice per year. Please note that we have established salary bands that ensures a fair and consistent approach for all applicants, eliminating the need for individual negotiations</li>
<li>23 days’ vacation leave increasing by 1 day each year to a maximum of 27 days. 6 public holidays plus 1 floating vacation day to use on a holiday of your choosing</li>
<li>Flexible, reasonable working hours and the chance to work from home for up to half of your working time</li>
<li>Private medical insurance with a company contribution, as well as dental and vision cover and life insurance</li>
<li>Retirement savings via a 401k plan with up to a 5% employer match</li>
<li>Paid funding for external education and study leave</li>
<li>Paid and unpaid sabbaticals based on length of service</li>
</ul>
Please click here to learn about our full reward package and the other benefits of working for Costello Medical: <a href="https://www.costellomedical.com/careers/benefits-package-in-the-us/" target="_blank">https://www.costellomedical.com/careers/benefits-package-in-the-us/</a>
The Application Process
You are required to submit your resume and a cover letter via our online application form. In your cover letter, you must explain why you think you would be suited to the role and why you would like to join Costello Medical, with examples to support both. Your resume should clearly state the dates of all qualifications and grades achieved where applicable.
Our recruitment process includes a telephone interview with a member of our Talent Acquisition team. Following this, you will also be sent a technical assessment, using R programming, and a proofreading exercise that we ask you to complete in your own time. If successful, you will be invited to an interview which will include a short presentation you can prepare for in advance. Our standard recruitment process lasts around 6 weeks, however, this can be adapted if necessary.
As an equal opportunity employer, we are committed to fostering a diverse and inclusive workforce and, throughout the recruitment process, there are a number of reasonable adjustments we can provide. Please click here to learn more.
Please note that, whilst we embrace AI to innovate and improve processes, your role may involve confidential data that cannot be uploaded to AI. Therefore, it is important for us to assess your own skills and abilities, so we recommend that you do not rely solely on this technology to generate any application materials.
Visa Sponsorship
We welcome applications from international candidates, but we are unfortunately unable to provide visa sponsorship for working visas. Therefore, you must have the right to work in the US independently from the company. However, we are able to consider those on a temporary visa, such as an OPT visa

Statistician

<h3>Job Description</h3>
Job DescriptionSalary: $26.00-$28.00 ph 
Our Mission At Texcell, our mission is to safeguard the medicines of today and tomorrow by providing essential services to the global biopharmaceutical industry. As experts in pharmaceutical sciences, our clients develop life-changing therapies for patients worldwide. As specialists in viral safety and bioassays, Texcell ensures the safety of these therapies throughout development. Together, we make medicines safe.

Our History Founded in 1987 at the Pasteur Institute in Paris, Texcells journey began with a laboratory team dedicated to addressing the HIV crisis. It was here that some of the earliest viral validation studies were conducted. Over the decades, weve continued to advance the science of viral safety, ensuring that patients can trust every dosetoday and in the future.
 
Position Summary
Contribute to the successful execution of viral clearance studies and diverse virology assays in a BSL-2, GLP, and cGMP regulated non-clinical CRO setting.
 
Key Responsibilities:
<ul>
<li>Perform routine cell culture activities for adherent and suspension cell lines, including thawing, seeding, feeding, passaging, and cryopreservation, in accordance with established SOPs.</li>
<li>Maintain cell cultures by monitoring cell morphology, confluency, viability, and growth characteristics, and report abnormalities promptly.</li>
<li>Conduct cell counting and viability assessments using hemocytometers and/or automated cell counters.</li>
<li>Execute basic cell-based assays and sample preparation as required, accurately recording data in laboratory notebooks or electronic systems.</li>
<li>Perform and/or support cell bank characterization and release testing, including sterility, mycoplasma, and other microbiological or cell-based assays.</li>
</ul>
<ul>
<li>Assist with executing viral clearance studies including spiking, sampling, and data collection per established protocols.</li>
<li>Perform virology assays proficiently and independently, including but not limited to:
<ul>
<li>TCID50 and plaque assays for viral infectivity and potency</li>
<li>qPCR for viral genome quantification</li>
</ul>
</li>
<li>Prepare sterile media, buffers, and reagents under cGMP conditions</li>
<li>Maintain accurate and real-time documentation of experiments, assays, and production activities in compliance with GLP/GMP/GDP standards.</li>
<li>Assist with routine and annual lab cleaning, equipment maintenance, and environmental monitoring.</li>
<li>Work outside of core business hours with occasional overtime, holidays and weekends as required.</li>
</ul>
 
Education &amp; Experience:
<ul>
<li>Bachelors degree in Biotechnology, Microbiology, Molecular Biology, or related life sciences field and 3+ years of relevant laboratory experience in cell culture, viral production, and/or virology assays in a regulated environment.</li>
</ul>

Skills &amp; Competencies:
<ul>
<li>Strong understanding of aseptic technique and BSL-2 regulatory/safety requirements.</li>
<li>Exceptional time management and organizational skills</li>
<li>Excellent communication skills both written and verbal</li>
<li>Keen attention to detail and problem-solving capabilities</li>
</ul>
<ul>
<li>Advanced computer skills Outlook, Excel, Teams, etc.</li>
</ul>

Viral Clearance Associate II

<h3>Job Description</h3>
Job Description
Mount Sinai Services at NYC Health+Hospitals/Queens is seeking a Chief of Hematology/Medical Oncology for the Queens Cancer Center at the Queens Hospital Center. This Center of Excellence is the only state-of the-art comprehensive cancer center in the NYC Health+Hospitals System. This is an excellent opportunity to work in a mission-driven institution whose goal is to deliver exceptional care to the community.
The qualified candidate will join a collaborative team of medical oncologists/hematologists, radiation oncologists, and surgeons to deliver a wide array of oncologic and hematologic services. Offering a range of services, the Queens Cancer Center is strongly committed to caring for the whole patient and places a strong emphasis on providing patient-centered care. The Queens Cancer Center is a Commission on Cancer-designated Community Cancer Program employing a multidisciplinary approach to cancer research and treatment.
The ideal candidate will contribute to the leadership, direction and integration of the oncology/hematology service line at Queens Hospital Center/Queens Cancer Center and participate in the well-established and robust clinical research program. The research mission of the Queens Cancer Center is to advance the field of cancer/hematologic treatments and preventive measures and to facilitate the availability of these advancements to the community we serve.
Minimum Position Qualifications:
· Possess a medical degree (MD/DO) from an accredited university
· Has or has the ability to obtain a New York State Medical License
· Board Certified in Hematology and Medical Oncology
· Minimum of 5+ years of clinical/leadership experience
· Excellent communication, bedside manner, and organizational skills
· Strong work ethic and desire to participate in a team-oriented, collaborative mission-driven institution
&nbsp;
All faculty have an academic appointment at The Icahn School of Medicine at Mount Sinai.
&nbsp;
Responsibilities include:
<ul>
<li>Deliver direct clinical hematology/medical oncology care to patients at the Queens Cancer Center/Queens Hospital Center, including outpatient clinic and in-patient consultation.</li>
<li>Work collaboratively with leadership to optimize effective use of resources and operational performance of the Cancer Center.</li>
<li>Work collaboratively with leadership to create new patient services and define expectations and standards of patient care.</li>
<li>Actively participate in relevant committees and programs, including Cancer Committee and weekly Multidisciplinary Tumor Board Conference, contributing to the overall excellence in hematology/medical oncology services.</li>
<li>Demonstrate high standards of care through collaboration with physicians, surgeons, clinical professionals and staff.</li>
<li>Contribute to medical and surgical education programs, by participating in teaching residents and medical students.</li>
<li>Be committed to a professional and patient-centered care environment that places a high priority on clinical excellence.</li>
</ul>
The Mount Sinai Health System (MSHS) provides equal employment opportunity to all its employees and applicants for employment without unlawful discrimination on the basis of their actual or perceived race, creed, color, religion, national origin, sex, gender, gender expression, gender identity, age, disability, marital or parental status, sexual orientation, veteran, immigration, citizenship, or other protected status. EOE including Veterans and Disabled
Company DescriptionWho We Are: Over 42,000 employees strong, the mission of the Mount Sinai Health System is to provide compassionate patient care with seamless coordination and to advance medicine through unrivaled education, research, and outreach in the many diverse communities we serve. Formed in September 2013, The Mount Sinai Health System combines the excellence of the Icahn School of Medicine at Mount Sinai with seven premier hospital campuses, including Mount Sinai Beth Israel, Mount Sinai Beth Israel Brooklyn, The Mount Sinai Hospital, Mount Sinai Queens, Mount Sinai West (formerly Mount Sinai Roosevelt), Mount Sinai St. Luke’s, and New York Eye and Ear Infirmary of Mount Sinai. 
<h3>Company Description</h3>
Who We Are:\r\nOver 42,000 employees strong, the mission of the Mount Sinai Health System is to provide compassionate patient care with seamless coordination and to advance medicine through unrivaled education, research, and outreach in the many diverse communities we serve.\r\n\r\nFormed in September 2013, The Mount Sinai Health System combines the excellence of the Icahn School of Medicine at Mount Sinai with seven premier hospital campuses, including Mount Sinai Beth Israel, Mount Sinai Beth Israel Brooklyn, The Mount Sinai Hospital, Mount Sinai Queens, Mount Sinai West (formerly Mount Sinai Roosevelt), Mount Sinai St. Luke’s, and New York Eye and Ear Infirmary of Mount Sinai.

Chief of Hematology/Medical Oncology

<h3>Job Description</h3>
Job Description
The function of Metrology Personnel is to ensure that all measuring equipment used for product inspection and acceptance performs to an established minimum standard and tolerance. Metrology personnel receive authority from and report to the Quality Manager/Quality Supervisor and exercises authority over no other employee.
Specific duties of Metrology personnel include but are not limited to:
1. Identify all company measuring equipment by applying a unique number to each unit.
2. Calibrate all measuring equipment, used to inspect Benoit products, on a scheduled basis.
3. Clean and lubricate measuring equipment at the time of calibration.
4. Affix calibration status decals on all measuring equipment after calibration.
5. Perform and document a Receiving Inspection and initial calibration on any new measuring equipment prior to use.
6. Perform and document receiving inspection on all threading inserts prior to use.
7. Maintain master gages and reference standards in such a manner to avoid deterioration or damage.
8. Maintain a clean, neat, well-equipped calibration lab.
9. Maintain clear, legible records to substantiate calibration activities for each piece of measuring equipment.
10. Alert the Quality Manager/Quality Supervisor to any potential problems which may arise due to faulty or nonconforming measuring equipment.
11. Perform any dimensional inspections assigned by the Quality Manager/Quality Supervisor.
Must be able to work in the United States without sponsorship, now or in the future.
Equal Opportunity Employer, Veterans, and Individuals with Disabilities, E-Verify
E-Verify Employer
Company DescriptionBenoit is a leading provider of premium threading, completion products, and engineered services for the upstream oil and gas industry. With 215,000 sq ft of total manufacturing space company-wide, we design and manufacture a comprehensive range of wellbore and running tools for exploration and production operations. With over 200 million feet of tubulars run worldwide and more than 400 deepwater and ultra-deepwater completions executed, we bring proven experience to every project. Our operations are guided by four core values: Service, Quality, Integrity, and Innovation. These principles shape our decisions, define our standards, and ensure consistent alignment across our organization. At Benoit, we believe our people are our greatest asset. We foster a diverse and inclusive workforce and offer a competitive compensation and benefits package that includes paid time off (PTO), holidays, health benefits, 401k profit sharing, basic and supplemental life insurance, long- and short-term disability coverage, and education assistance. If you are driven and seeking to contribute your skills to a company with a strong legacy, proven performance, and a forward-looking vision, we invite you to apply. 
<h3>Company Description</h3>
Benoit is a leading provider of premium threading, completion products, and engineered services for the upstream oil and gas industry. With 215,000 sq ft of total manufacturing space company-wide, we design and manufacture a comprehensive range of wellbore and running tools for exploration and production operations. With over 200 million feet of tubulars run worldwide and more than 400 deepwater and ultra-deepwater completions executed, we bring proven experience to every project. Our operations are guided by four core values: Service, Quality, Integrity, and Innovation. These principles shape our decisions, define our standards, and ensure consistent alignment across our organization. \nAt Benoit, we believe our people are our greatest asset. We foster a diverse and inclusive workforce and offer a competitive compensation and benefits package that includes paid time off (PTO), holidays, health benefits, 401k profit sharing, basic and supplemental life insurance, long- and short-term disability coverage, and education assistance. If you are driven and seeking to contribute your skills to a company with a strong legacy, proven performance, and a forward-looking vision, we invite you to apply.

Metrologist

<h3>Job Description</h3>
Job Description
Description
Work closely with the Senior Chemist and/or Technical Director to improve the functionality, performance, and application of chemical products. Adjust, refine, or optimize existing product formulations based on feedback from sales engineers, field service personnel, and customers. Replicate specific water qualities and system conditions to conduct testing of new and existing products, ensuring accuracy and relevance to real-world applications. Review, perform, and verify quality control parameters to support consistent production standards. Prepare documentation, technical reports, and presentations as required by the Senior Chemist and/or Technical Director. Maintain accurate laboratory records, test data, and research files in accordance with internal documentation standards. Collaborate with the R&amp;D and QC teams to support product troubleshooting, root-cause analysis, and continuous improvement initiatives. Follow all laboratory safety protocols and maintain clean, organized, and compliant laboratory workspaces. Perform other duties and special projects as assigned.
Additional Skills &amp; Qualifications
The Research &amp; Development Chemist supports the development of new products, enhancement of existing formulations, and testing efforts required for innovation and continuous product improvement. This role also supports Proton Software by providing accurate data, application insights, and testing results that inform internal and external stakeholders.
Experience Level
Entry Level
Job Type &amp; Location
This is a Contract to Hire position based out of Plant City, FL.
Pay and Benefits
The pay range for this position is $24.00 - $26.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Plant City,FL.
Application Deadline
This position is anticipated to close on Jan 26, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

R&D Chemist

<h3>Job Description</h3>
Job Description
Contact: Neisha Camacho/Terra Parsons - No 3rd party candidates Job Summary: The Biostatistician II is responsible for having a working knowledge of all related processes with the ability to independently lead a study, support analysis, and provide high-quality documents to support sponsors' research programs. The ideal candidate is a Biostatistician with strong applied SAS skills (including TFLs, inferential analyses, and randomization) who can collaborate cross-functionally with the programming team, while also independently contributing to statistical deliverables and quality review. Experience working on Phase 1 clinical trials is highly desirable, particularly with first-in-human and dose-escalation studies, including PK/PD data and early safety endpoints. Key Responsibilities
<ul>
<li>Follow department and company standard operating procedures (SOPs), forms, templates, and policies.</li>
<li>On occasion, may act as senior Biostatistician for simple to complex studies and be the central point of contact for the assigned Biostatistics team, extended internal project team, and the client.</li>
<li>Provide input for Biostatistics portion of project timelines.</li>
<li>Review protocols for simple to complex studies.</li>
<li>Generate randomization schedules using SAS or randomization-specific software.</li>
<li>Develop and QC statistical analyses for simple to complex studies.</li>
<li>Develop or assist in developing the Statistical Analysis Plans (SAPs) and related table, figure, and listing (TFL) shells.</li>
<li>Develop tables of summary statistics and graphics for clinical trials.</li>
<li>Assist in answering deficiency letters from regulatory agencies, as required.</li>
<li>Utilize SAS to validate statistician programs and results.</li>
<li>Perform QC review of analyses and documents prepared by others.</li>
<li>Oversee nonclinical projects, work with line manager to direct activities of other Biostatisticians.</li>
<li>Coordinate with internal teams to deliver quality documents on time.</li>
<li>Represent Biostatistics in client and inter-departmental meetings.</li>
<li>Conduct all work in compliance with SOPs, GCP, and regulatory guidelines.</li>
<li>Maintain familiarity with client/internal expectations and ensure aligned analyses and documentation.</li>
<li>Stay current on global regulatory requirements (FDA, EMA, ICH, GCP).</li>
<li>May participate in or lead quality improvement initiatives.</li>
<li>Other duties as assigned.</li>
</ul>

Education: Master's Degree in Statistics or a related field required.
Core Competencies
<ul>
<li>Excellent verbal and written communication</li>
<li>Ability to communicate proactively and clearly with cross-functional teams to ensure alignment on study timelines, deliverables and issues.</li>
<li>Professional attitude and strong interpersonal skills</li>
<li>Collaborative, client-focused mindset</li>
<li>Flexible with work assignments and learning</li>
<li>Strong organizational and prioritization skills</li>
<li>High attention to detail</li>
<li>Understanding of clinical research life cycle and regulations</li>
<li>Proficient in Microsoft Word, Excel, PowerPoint</li>
</ul>
Statistical &amp; Technical Skills
<ul>
<li>Own statistical deliverables from design through analysis (e.g., SAPs, TFLs)</li>
<li>Moderate SAS programming proficiency, including the ability to perform inferential statistical analyses</li>
<li>Review programming output for accuracy and alignment with SAP</li>
<li>Protocol review</li>
<li>Review of aCRF / eCRF</li>
<li>Creating and reviewing SAPs</li>
<li>Creating and writing TFL specs and shells</li>
<li>Understanding of CDISC standards (SDTM, ADaM)</li>
<li>SDTM specifications and domain review</li>
<li>ADaM specification writing and domain review</li>
<li>ADRG (Analysis Data Reviewer’s Guide) creation and review</li>
<li>Pinnacle 21 review and input</li>
</ul>

Biostatistician - Remote

<h3>Job Description</h3>
Job DescriptionLCMS Lead Scientist
Job Description
As a LC-MS Lead Scientist, you will play a pivotal role in overseeing bioanalytical studies, ensuring that all methods meet regulatory and client requirements. You will not be working directly in the lab but will be responsible for reviewing data, signing off on reports, and acting as the primary scientific point of contact. Your expertise will guide the bioanalytical study work, and you will coordinate with regulators and stakeholders, both internally and externally.
Responsibilities
<ul>
<li>Oversee studies and ensure all methods are prepared, validated, executed, and documented to meet regulatory and client requirements.</li>
<li>Sign off on reports and approve raw data.</li>
<li>Act as the primary scientific point of contact for studies.</li>
<li>Coach and indirectly guide a team of up to 20 members.</li>
<li>Coordinate across internal and external stakeholders, including discussions with regulators for clinical or pre-clinical studies.</li>
<li>Travel up to 10% for cross-site or client visits.</li>
</ul>
Required Skills
<ul>
<li>B.S. or Masters in Life Sciences (Chemistry, Biology, Biochemistry, etc.).</li>
<li>2-3 years of LCMS experience.</li>
<li>Experience as a Lead Scientist with 1-5 years (LS1) or 7-9 years (LS2) of experience.</li>
<li>Must have experience as a Lead Scientist/Responsible Scientist/Principle Investigator in the Bioanalytical sector (GLP or GCP regulations).</li>
<li>Full responsibility over the study, with experience in BioA CRO regulated space.</li>
<li>LBA (Ligand Binding Assay) experience, including data review/approval, protocol/sample analysis plan development, and method validation readiness.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with Sciex Mass Spec and analysis software.</li>
<li>Familiarity with LIMS, Nautilus, and Analyst software.</li>
<li>Knowledge of ICH or 28BMV regulatory guidance protocols and FDA internal standards.</li>
</ul>
Work Environment
The role is based in a lab setting within the Bioanalytical team, consisting of approximately 100 employees, including 60 chemists. This is a hybrid position, requiring 2-3 days onsite per week, with flexibility on the days but consistency each week. The role involves indirect reporting from method development chemists, validation chemists, sample analysis, and report writing. The work is workload-based rather than project-based, with a varying number of projects depending on client needs. The team is expanding, with current plans to increase from 16 to 18 members in Madison. Travel is limited, with a maximum of 10% required for client visits or conferences.
Job Type &amp; Location
This is a Permanent position based out of Madison, WI.
Pay and Benefits
The pay range for this position is $85000.00 - $110000.00/yr.
Medical Plan* No Charge Laboratory Testing Benefit and physical therapy Dental Plan Vision Plan Flexible Spending Accounts (FSAs) Health Care FSA Dependent Care FSA Disability Plan Short Term Disability (STD) Long Term Disability (LTD) Life and Accidental Death and Dismemberment (AD&amp;D) Insurance Plans Basic Life Optional Life Dependent Life Optional AD&amp;D Employee Stock Purchase Plan (ESPP)
Workplace Type
This is a hybrid position in Madison,WI.
Application Deadline
This position is anticipated to close on Jan 26, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

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