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<h3>Job Description</h3>
Job Description
Job Title: Research Associate
Location: La Jolla, CA US 92037
Duration: 06-12 months of Contract (with possible extension)
Shift Available: 9:00am to 5:00pm (Monday – Friday)
Pay rate - $32.00/hr.
&nbsp;
Job Description
External Research Solutions (ERS) supports scientific innovation by managing external screening partnerships and ensuring seamless data integration between internal teams and external vendors. Our mission is to enable high-quality, efficient research through robust data operations, strong vendor collaboration, and disciplined data governance.
Role Overview
Support external screening data operations and vendor coordination to ensure accurate, timely data delivery for scientific decision-making.
&nbsp;
Key Responsibilities
• Maintain and update external screening data repositories and vendor-specific portals.
• Process screening requests, validate and QC data deliverables, and distribute accurate data to scientists.
• Receive, format, and publish screening data using standardized data-loading tools and templates.
• Register and maintain vendor profiles and project records in designated systems.
• Maintain and update reference/control compound lists and screening protocols.
• Request registration of new control/reference compounds as needed.
• Adhere to established data handling standards and maintain clear documentation for audits and reporting.
&nbsp;
Qualifications
• Bachelor’s degree in Life Sciences, Data Management, or a related field (or equivalent experience).
• Experience in scientific data workflows and management
• Lab experience with invitro screening assays desired
&nbsp;
Competencies &amp; Behavioral Skills
• Strong attention to detail with excellent organizational and communication skills.
• Ability to manage multiple priorities in a fast-paced, cross-functional environment.
• Collaboration: Builds strong relationships across teams and with external partners.
• Adaptability: Responds effectively to changing priorities and evolving processes.
• Accountability: Takes ownership of deliverables and follows through to completion.
• Customer Focus: Anticipates the needs of scientists and stakeholders to improve service quality.
• Continuous Learning: Seeks opportunities to enhance knowledge of tools and best practices.
Company DescriptionSelect Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs. Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities 
<h3>Company Description</h3>
Select Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs.\r\n\r\nBased in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities

Research Associate

<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
Bio-statistician is required to conduct statistical analysis, modelling, and reporting activities in pharmaceutical industry.

Biostatistician

<h3>Job Description</h3>
Job Description
Compounder – 1st Shift
Location: Shakopee, MN
Schedule: Monday–Friday, 6:30 AM to 5:00 PM
Pay: $23/hour
 
Job Summary:
We’re looking for a reliable Compounder to join our team! You’ll be responsible for compounding and blending raw materials based on specific formulas to ensure high-quality finished products. This is a hands-on role ideal for someone with strong attention to detail and a background in industrial mixing or chemical environments.
&nbsp;
Key Responsibilities:
- Accurately mix and blend raw materials per formulas
- Prepare equipment and inventory before each batch
- Clean tanks, hoses, and work areas according to safety and sanitation standards
- Support production lines as needed
- Collaborate with R&amp;D, QA, and Production teams on formulas and feasibility
&nbsp;
Requirements:
- High School diploma or GED
- 1–3 years of industrial mixing/blending experience (chemical background preferred)
- Basic chemistry and strong math skills
- Able to operate forklift, tank mixers, PH meters, pumps, and other equipment
- Physically able to lift 50–100 lbs and stand for long periods

Chemical Compounder- 1st Shift

<h3>Job Description</h3>
Job Description
Ironwood Cancer &amp; Research Centers has beautiful state-of-the-art integrated Cancer and Women's Centers, with locations strategically located throughout the Valley. Each one provides a superior cancer care environment with a full spectrum of cancer related services for patients. Our multi-disciplinary team approach includes surgical oncology, medical oncology, radiation oncology, women's centers, diagnostic imaging services, social service support, nutritionist, integrative services, and genetic counseling.
Mission Statement: To serve the community by providing quality, comprehensive cancer care which respects the values and needs of each individual.

Overview: We are looking for a qualified and experienced Physicist to work in our fast-paced out-patient oncology clinic. The Medical Physicist conducts all aspects of radiation therapy physics, including clinical medical physics support, equipment calibration and commissioning, maintenance of appropriate quality assurance programs for equipment and treatment delivery, compliance with radiation safety, licensing issues and other pertinent regulatory requirements. 
Schedule: Full-time, Monday through Friday day shift position. 
Essential Duties and Responsibilities: 
<ul>
<li>Responsible for all physics of radiotherapy treatments.</li>
<li>Responsible for Calibration and QA of all treatment devices.</li>
<li>Responsible for Calibration and QA of treatment simulators.</li>
<li>Responsible for Calibration and QA of treatment planning systems.</li>
<li>Responsible for Calibration and QA of the physics test equipment.</li>
<li>Review of treatment plan calculations.</li>
<li>Review of weekly chart checks.</li>
<li>Commissioning of new radiologic systems.</li>
<li>Establish new commission &amp; QA criteria for new radiologic programs.</li>
<li>Establish new treatment protocols for safe and effective treatment delivery.</li>
<li>Consult with and assist radiation therapists, dosimetrists and radiation oncologists.</li>
<li>Provide training for new clinical systems and programs.</li>
<li>Provide radiation safety training.</li>
<li>Provide treatment planning for special procedures like HDR and SBRT.</li>
</ul>
Knowledge and Skills:
<ul>
<li>Ability to communicate frequently with front office staff, radiation therapists, dosimetrists, other physicists and radiation oncologists. Must be able accurately exchange detailed information in each situation.</li>
<li>Must remain calm and solve problems in highly stressful situations with limited time.</li>
<li>Constantly working around occupational levels of radiation exposure and hazardous materials.</li>
<li>Constantly operates computer and office equipment.</li>
<li>Must be able to maintain stationary position for up 6 hours per day.</li>
<li>Must be able to read medical charts on a computer screen for up to 6 hours per day.</li>
<li>Ability to use office equipment, computer, and typing is essential.</li>
</ul>
 Education and Experience:
<ul>
<li>Master’s Degree or PhD in Medical Physics or closely related field.</li>
<li>2 years clinical experience.</li>
</ul>
We offer a competitive salary and a comprehensive benefit package including health/dental/vision and life insurance, 401K, and a caring work environment. We are an E.O.E.
Please visit our website at <a href="http://www.ironwoodcrc.com" target="_blank">www.ironwoodcrc.com</a>. "Outsmarting Cancer One Patient at a Time"

Physicist - Medical

<h3>Job Description</h3>
Job DescriptionAbout Autocam/NN Inc.
We manufacture high‑performance precision components and pair innovative thinking with advanced machining to redefine what’s possible. Our success starts with people—now we’re seeking a Process Chemicals Laboratory Associate.
Role focus
Support stable, efficient automotive production by ensuring process chemicals are on target and well documented, while assisting teammates and the Chemist with research and rework.
Key responsibilities
<ul>
<li>Monitor, evaluate, and analyze chemicals used in automotive production to support effective and efficient operations.</li>
<li>Measure, record, analyze, and maintain required concentration levels to keep processes in control.</li>
<li>Create accurate charts and graphs to report chemical concentrations.</li>
<li>Execute project and research tasks as directed by the Chemist.</li>
<li>Rework parts as needed, including deburring and derusting.</li>
<li>Evaluate cleaning chemicals for suitability and performance.</li>
</ul>
Minimum qualification
<ul>
<li>Completion of at least 2 years of school toward a chemistry degree.</li>
</ul>
Bring your analytical mindset and attention to detail to a place where your work directly supports quality and throughput.

Process Chemicals Laboratory Associate

<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 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 DescriptionRole Summary
<ul>
<li>Responsibilities: You will be responsible for leading a range of projects that involve 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: $100,000 per annum</li>
<li>Benefits: Hybrid working options, generous holiday allowance, flexible working hours, private medical and dental insurance, 401K plan, life insurance, full funding for external training, comprehensive travel insurance and more</li>
<li>Role Type: Full-time, permanent </li>
<li>Start Date: We are currently recruiting for start dates throughout 2026 and you will be asked to state your preference on your application form</li>
<li>Location: This role is available in our Boston, MA and New York, NY offices</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.
The Senior Statistician will lead statistics projects, working very closely with the Consultant or Team Lead as well as colleagues from all specialities, to ensure that statistics projects are delivered to an exceptionally high standard, on time and in line with client expectations. This involves providing strategic advice to clients at project initiation, supervising the project team and regular interaction with external stakeholders by teleconference, email and in person. The Senior Statistician will also be central to the quality control of the project, involving the review of colleagues' work and the provision of constructive feedback.
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 service 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>
You will also play a key role in contributing to business development by developing and maintaining excellent client relationships and identifying opportunities to provide additional services to clients within projects. There may also be opportunities to line manage and mentor our Statistician Interns.
Career Progression
Senior Statisticians are supported to progress to the Consultant Statistician role. Consultant Statisticians manage a range of projects and have full responsibility for client communication on projects, as well as leading budgeting plans and business development efforts. In addition to technical project delivery, Consultant Statisticians line manage team members and have internal responsibilities spanning areas such as recruitment and training.
To learn more about the personal and professional development opportunities at Costello Medical, explore first-hand career profiles from our colleagues about their experiences with the company: <a href="https://www.costellomedical.co.uk/careers/working-at-costello-medical/" target="_blank">https://www.costellomedical.co.uk/careers/working-at-costello-medical/</a>
About Costello Medical
Costello Medical is a rapidly growing global healthcare agency specialising 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 organisations. We have been listed in the Top 100 Best Companies to Work For list since 2017 and were proud to receive B Corporation accreditation in 2022. Learn more about us, our work, and our mission on our website: <a href="https://www.costellomedical.com/" target="_blank">https://www.costellomedical.com/</a>
Requirements
About You
We are looking for individuals who are collaborative, self-motivated and enthusiastic, with a strong and demonstrable background in the HEOR sector. You will take pride in producing exceptionally high-quality work and will relish the opportunity to build successful client relationships. You will identify and capitalise on opportunities to go above and beyond for clients and exceed their expectations wherever possible. You will be someone who has a genuine desire to play an active role in the development of our growing team. You will enjoy using your experience to train and mentor others and will be skilled at delivering effective feedback to support your colleague’s professional development. 
You will thrive in a fast-paced environment, be highly organised and able to manage timelines across multiple projects. Additionally, you will be willing to step up and support your project team as needed.
This role is suited to those who have professional experience, of typically no less than 2 years, in applying economic and mathematical modelling techniques within an industry setting, ideally within a pharmaceutical, medical devices or consulting company. Specifically, we are looking for candidates with experience: 
<ul>
<li>Working directly with clients from project initiation to completion</li>
<li>Leading a project team, including delegating tasks and managing the time of others coupled with the ability to manage timelines across multiple projects at once and the flexibility to respond to changing deadlines</li>
<li>Communicating directly with clients including responding to different communication styles, as well as a proven ability to build robust and sustainable client relationships</li>
</ul>
In addition, essential requirements for the role are:
<ul>
<li>A degree level or higher qualification in a scientific or mathematical discipline (minimum GPA 3.3) is required. A focus on statistics and data analysis is essential</li>
<li> The technical and mathematical ability, coupled with exceptional written and oral communication skills, to explain complex techniques and results to non-experts, and to teach and mentor others in the Statistics team</li>
<li>An excellent understanding of and extensive experience in the R programming language, and the willingness and ability to rapidly develop your programming skills</li>
<li>A willingness to trial, explore or recommend new software or techniques that may suit specific projects</li>
<li>Exceptional attention to detail and a high degree of accuracy in technical and written work, along with the ability to maintain exceptional customer service and the quality of deliverables under multiple competing demands</li>
<li>The ability to use your initiative and work independently, in addition to working collaboratively within project teams</li>
<li>Excellent written English is fundamental; this 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 Stan, Python, SQL, or other programming languages used for data analysis</li>
<li>Awareness of data standards for clinical research and statistical analysis (e.g. CDISC, SDTM, ADaM, ICH Statistical Principles for Clinical Trials)</li>
</ul>
Benefits
What We Offer
<ul>
<li>A starting salary of $100,000 per annum</li>
<li>A discretionary profit share bonus paid twice per year</li>
<li>Private medical insurance with a company contribution </li>
<li>Dental and vision cover </li>
<li>23 days’ vacation leave increasing by 1 day to a maximum of 27 days. 6 public holidays plus 1 floating holiday </li>
<li>The chance to work from home for up to half of your working time</li>
<li>Retirement savings via a 401k plan</li>
<li>Paid funding for external education and study leave</li>
<li>Life insurance </li>
<li>Comprehensive travel insurance</li>
<li>Flexible and reasonable working hours</li>
<li>Regular company-funded social activities </li>
</ul>
Please click here to learn about our 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.
Then, our recruitment process includes a telephone interview with a member of the Talent Acquisition team, followed by an assessment for 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 1 month, 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: <a href="https://www.costellomedical.com/reasonable-adjustments/" target="_blank">https://www.costellomedical.com/reasonable-adjustments/</a>
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.

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