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<h3>Job Description</h3>
Health Physicist/Radiation Safety Officer at West Physics
 
About the Job:
Position Title: Health Physicist/RSO
Location: Macon, GA
Salary: Based on training and experience
Hours: Full-time / full benefits
<a href="http://www.westphysics.com" target="_blank">www.westphysics.com</a>
 
Description of position:
West Physics has an immediate opening for an experienced Health Physicist/Radiation Safety Officer based in Macon, GA. This position requires a solid educational background in health physics, a strong interest and aptitude for learning, and a can-do attitude with an excellent work ethic. The successful candidate should possess strong leadership, communication, and management skills. This position is best suited to someone with excellent interpersonal skills, outstanding written and verbal communication, the ability to work independently and as part of a project team, and strong technical proficiency. The ability to exercise high responsibility and autonomy (once trained) is integral to this position. This position may require occasional travel, typically 10 days per month, depending on the number and location of specific consulting assignments. This position offers substantial opportunities for professional, educational, and financial growth and development; as such, the candidate should be seeking long-term employment opportunities.
West Physics has been recognized by Inc. 5000 11 times as one of the fastest-growing companies. As a result of this growth, we are seeking a dynamic candidate to join our technical team of over 100+ physicists across the United States. 
We strongly encourage you to apply today! 
 
Primary Responsibilities:
<ul>
<li>Answer radiation safety and health physics questions from client personnel.</li>
<li>Assist client personnel with radiation safety-related compliance activities.</li>
<li>Perform nuclear medicine, diagnostic radiology, and industrial and academic radiation safety audits.</li>
<li>Perform radioactive materials (RAM) licensing activities on behalf of clients, including license applications, renewals, potential enforcement activity, consulting activity, and response.</li>
<li>Perform dosimetry review, worker and patient dose estimates, and fetal dose estimates.</li>
<li>Perform source inventory, leak-testing, and other radiological assay and analysis operations.</li>
<li>Conduct dose investigations and ALARA reviews.</li>
<li>Perform shielding designs and conduct shielding verification testing.</li>
<li>Assist health physicists and senior health physicists with more complex consulting duties.</li>
<li>Assist medical physicists and senior medical physicists with periodic diagnostic radiology equipment testing.</li>
<li>Data review for CT, PET, fetal dose, etc.</li>
<li>Other related duties as needed.</li>
</ul>
 
Prerequisites:
<ul>
<li>Bachelor's (B.S.) or Master's (M.S.) degree in Health Physics or a physics-related discipline. (Medical Physics, Nuclear Engineering, etc.)</li>
<li>Mid-career health physicists will be considered who have (2+) years of professional full-time experience in a health physics role that includes medical and applied health physics applications, as well as other areas such as research, academia, or industrial applications. (strongly preferred)</li>
<li>RSO-eligible: must show evidence of holding a medical radioactive materials license in categories 10CFR 35.100, 35.200, and 35.300 (or equivalent Agreement State categories) or be immediately eligible for a preceptor to hold such licenses. Upon hire, this position will be immediately appointed to hold licenses for clients as a statutory RSO.</li>
<li>Familiarity and proficiency with basic health physics activities (e.g., survey instrument used, survey technique, leak testing, dosimetry review, etc.) and a willingness and aptitude to master more advanced health physics skills and activities.</li>
<li>The ability to understand and apply regulations from various State and Federal entities to different client situations and write effective policy and procedures, Radiation Safety Manuals, and user-friendly forms.</li>
<li>Solid foundation in radiation physics, radiation biology, electronics, and other areas relevant to equipment quality assurance testing. Preferred not required</li>
<li>Effective written and oral communication skills, including professional, courteous, and convincing or persuasive in discussions with clients, regulators, and colleagues.</li>
<li>Strong technical proficiency, the ability to manage multiple complex assignments concurrently and to completion, strong attention to detail, and the ability to deliver exceptional client service.</li>
<li>Excellent time management and organizational skills.</li>
<li>A working knowledge of MS Office Suite (Word, Excel, PowerPoint) and excellent general computer skills. Familiarity with Apple computers (i.e., macOS) and applications is a plus.</li>
<li>The candidate must be willing and open to being trained on new opportunities and activities to enhance their technical skill set.</li>
<li>Applicant must have a valid U.S. Driver's License</li>
<li>Applicant must be authorized to work in the U.S.</li>
</ul>
 
Compensation &amp; Benefits:
<ul>
<li>Medical/Dental/Vision/Life/Short-Term Disability insurance</li>
<li>Generous vacation/sick time policy</li>
<li>401(k) with company matching</li>
<li>8 paid holidays</li>
<li>Flexible Spending Account – Medical and Dependent Care</li>
<li>Continuing Education: Company-paid maintenance for state/or national-level certifications &amp; credentials</li>
<li>Relocation Assistance</li>
<li>Generous meal per diem, travel reimbursements &amp; hotel accommodations for qualifying work travel</li>
<li>State-of-the-art test equipment, phantoms, and computational resources, as well as best-in-class software, with in-house IT support </li>
</ul>
 
About West Physics:
West Physics is a nationwide provider of medical and health physics services. “WP” takes pride in offering the highest level of expertise, flexibility, and commitment to thousands of customers in 50 U.S. States, federal territories, the Caribbean, Latin America, and the Middle East. WP is headquartered in Atlanta, GA, and with the addition of numerous field office locations across the U.S., we can ensure a high level of customer service to our domestic and international clientele. Among our clientele are many major medical centers, equipment manufacturers, and accreditation bodies. We specialize in providing expert radiation safety, consulting, and testing services and addressing complex technical and regulatory problems for clients around the world. WP maintains the very finest test equipment and computational and administrative resources to serve and support our technical staff.
 
West Physics has been recognized by the Inc. 5,000 a total of 10 times as one of the fastest-growing companies in the United States. West Physics is committed to the highest standards of ethics in everything that we do. We believe strongly that our customers are entitled to fair treatment and absolute honesty in every transaction. Therefore, we are a proud member of the U.S. Better Business Bureau and have earned their highest possible ranking (A+).
 
Interested candidates should submit their resumes to <a href="mailto:mark.broomfield@westphysics.com" target="_blank">mark.broomfield@westphysics.com</a>
 
West Physics Mission Statement
“To be the pre-eminent provider of medical and health physics services by delivering outstanding, relentlessly improving customer service and technical expertise, and in so doing, to improve the happiness of our customers and the quality of medical diagnosis and radiation safety for as many human beings as possible.”
 
Equal Opportunity Employer Veterans/Disabled

Health Physicist/Radiation Safety Officer

<h3>Job Description</h3>
Please note: For confidentiality purposes, this position is not located in Blue Bell. The role is based in the tri-state area.
 
This role will focus on the validation of analytical methods for products in development or for commercial products when needed. This position involves executing validation studies and optimizing or developing analytical methods when needed to support drug product applications. In addition to analytical method validation, this position will involve R&amp;D T0 and Stability testing for 2-3 drug products in development
 
Key responsibilities. 
<ul>
<li>Develops analytical methods that are accurate, precise, and specific for use in both the Quality Control department and the Research department. Methods primarily include HPLC and GC but also include ICP-MS, Karl Fisher, solid-state characterization, and others.</li>
<li>Documents the development of the method in the appropriate notebooks for future reference. Performs pre-validation work ahead of transfer to the Validation Department to demonstrate suitability for use.</li>
<li>Prepares test method procedures and supporting documentation for use in the Quality Control laboratory.</li>
<li>May be required to develop validation protocols and validate analytical methods used in the testing of raw materials, intermediate products, final products, and cleaning samples.</li>
<li>Assists in the maintenance and calibration of laboratory analytical instrumentation including, but not limited to HPLC and GC. Maintains accurate records regarding the maintenance and calibration activities.</li>
<li>May support manufacturing operations with testing of raw materials, intermediate products, final products, and cleaning samples. The incumbent is expected to operate in a neat and orderly manner and to provide accurate and timely test results.</li>
<li>Assists in the maintenance of the QC Laboratory. In addition to routine housekeeping and glassware cleaning, maintains and appropriate inventory of supplies and chemicals.</li>
<li>Documents sample preparation, equipment set-up and test results in Laboratory Notebooks or on the appropriate test record form. Documentation must be complete and verified by a second member of the quality group. In addition, laboratory log sheets, those related to equipment usage, calibration, and maintenance, reference standard inventory, QC chemical inventory, or those related to retention samples will be properly maintained.</li>
</ul>
 
EDUCATION/EXPERIENCE. 
<ul>
<li>A Bachelor’s Degree in Chemistry (Master's or PhD Degree is preferred)</li>
<li>A minimum of 7 years of experience in small molecule pharmaceutical laboratories, with a strong background/proficiency in LC, GC, Dissolution and chromatographic method validation and development.</li>
<li>Proficient with Empower software. </li>
<li>Strong organizational skills.</li>
<li>Good communication skills</li>
<li>Good writing skills.</li>
</ul>

Research And Development 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 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
A well-established steel manufacturer is seeking a hands-on Lab Supervisor to lead a small team in its chemical and physical testing lab. You’ll oversee daily testing on metal products, ensure quality compliance, and keep production moving by working closely with engineering and operations.
This is a great fit for someone with 3+ years in a metals or industrial lab and some leadership experience who’s ready to take ownership and make an impact.
What You’ll Do:
<ul>
<li>
Supervise and train lab technicians across multiple shifts
</li>
<li>
Review production orders and assign required testing
</li>
<li>
Perform or oversee testing on steel and metal samples
</li>
<li>
Maintain calibration, accuracy, and lab safety standards
</li>
</ul>
What You’ll Bring:
<ul>
<li>
Experience in steel, foundry, or industrial lab environments
</li>
<li>
Knowledge of chemical or mechanical testing methods
</li>
<li>
Strong leadership and communication skills
</li>
</ul>
Join a growing manufacturer with a great culture, long-term stability, and room to advance.

Lab Supervisor

<h3>Job Description</h3>
Job DescriptionSalary: $48K-$52K, depending upon experience 
Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to build lasting partnerships that enable the life sciences industry to accelerate discovery and innovation in research and manufacturing. We can offer you the chance to build on your skills and knowledge while working among experts in their fieldsand with cutting-edge instrumentation.

Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment.We aim to recruit the best people who stand out among their peers and embody our Core Values:

<ul>
<li>Client Focused: We only succeed when our clients succeed.</li>
<li>Outstanding: We deliver meticulous results through outstanding performance.</li>
<li>Good: We act ethically and morally.</li>
<li>Employee-Centric: We honor and support our employees.</li>
<li>Nimble: We are prepared to adapt in an ever-changing industry.</li>
<li>Team-Oriented: We collaborate with each other and with our clients.</li>
</ul>
 
We currently have a role available for a Bioanalytical Chemist with industrial pharma lab experience.
 
Job duties include, but are not limited to, the following:
 
<ul>
<li>Perform routine &amp; non-routine LC/MS analyses.
<ul>
<li>Sciex/Analyst experience preferred.</li>
</ul>
</li>
<li>Develop and optimize LC/MS analytical methods.</li>
<li>Consistently produce standard curve and QC data that meet established validated assay criteria.</li>
<li>Operate and perform basic, routine maintenance and diagnostics on HPLC and mass spectrometers.</li>
<li>Use the LC/MS software to perform routine data processing.</li>
<li>Accurately prepare and label laboratory reagents, solutions and samples.</li>
<li>Consistently utilize data file nomenclature and organizational conventions.</li>
<li>Track study submissions on the analyst/customer collaboration site.</li>
</ul>
 
Job requirements include, but are not limited to:
 
<ul>
<li>BS-Chemistry (or related field) with 0-2 years of industrial experience.</li>
<li>Proactively maintaining productivity with strong attention to detail.</li>
<li>Excellent communication skills verbal and written. Ability to communicate issues as they occur.</li>
<li>Works well both as a team and as an individual.</li>
<li>Strong safety focus and willingness to assist with general lab housekeeping.</li>
<li>Ability and willingness to adapt to changing project needs and timelines.</li>
</ul>
 
This job posting will close by 2/28/2026 or when a candidate is identified, whichever comes first.

Bioanalytical Chemist

<h3>Job Description</h3>
Job Description
This is a remote position.
The Biostatistician will play a critical role in designing, analyzing, and interpreting clinical trial data to support drug development and regulatory submissions. This position collaborates with clinical, data management, and regulatory teams to ensure statistical rigor in trial design, data analysis, and reporting. The ideal candidate brings strong analytical skills, regulatory knowledge, and proficiency with statistical programming tools. Key Responsibilities: Collaborate with clinical and regulatory teams to design statistically sound clinical trials (e.g., sample size calculation, randomization methods). Develop and review statistical analysis plans (SAPs) in compliance with regulatory guidelines. Perform statistical analyses using SAS, R, or other statistical software on clinical trial datasets. Interpret results and present findings in clinical study reports, regulatory submissions, and scientific publications. Provide statistical support during protocol development, including endpoints and methodology. Ensure statistical deliverables meet internal quality standards and regulatory requirements (e.g., FDA, EMA, ICH). Review case report forms (CRFs) and data validation rules for accuracy and consistency with statistical needs. Collaborate with Data Management and Clinical Operations to ensure data integrity and resolve data discrepancies. Stay up to date on industry best practices, methodologies, and relevant regulatory guidance. Minimum Qualifications: Master’s or Ph.D. in Biostatistics, Statistics, Mathematics, or a related quantitative field. Minimum of 3 years (for MS) or 1 year (for PhD) of relevant experience in the pharmaceutical, biotechnology, or CRO industry. Proficient in statistical programming languages such as SAS and/or R. In-depth knowledge of ICH-GCP, CDISC standards (SDTM, ADaM), and regulatory guidance documents. Strong understanding of clinical trial design, methodology, and regulatory requirements. Excellent communication skills with the ability to interpret and present statistical findings clearly. Strong attention to detail and a commitment to data quality and accuracy. In addition to a dynamic and collaborative work environment, we offer a comprehensive benefits package to support our employees' well-being. Our benefits include paid holidays, Paid Time Off (PTO) policy, and medical insurance to ensure our team members have the flexibility and coverage they need. We believe in fostering a healthy work-life balance while providing the necessary support for professional and personal growth. Be part of our network of Subject Matter Experts. E-Verify Participation: Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. For more information on E-Verify, please contact DHS at 888-897-7781 or through their website at dhs.gov/e-verify.

Biostatistician

<h3>Job Description</h3>
Trident Consulting is seeking a " Chemistry Expert 2” for one of our clients. A global leader in business and technology services.
 
Position: Chemistry Expert 2
 Location: Cleveland, OH
 Mode: Contract 
<ul>
<li>2nd Shift: 2:00 PM – 10:30 PM, Monday–Friday</li>
<li>40 hours/week, 8 hours/day</li>
</ul>
Position Overview
Research Organics, LLC is seeking an experienced QC / Analytical Chemist to support Quality Control operations due to a spike in business needs. The role focuses on wet chemistry testing, HPLC analysis, method validation, and GMP-compliant documentation, with responsibility for independent testing, data review, investigations, and technical support of protocols and reports.
This position requires a highly self-motivated, detail-oriented laboratory professional capable of working independently with minimal supervision while maintaining strict adherence to GMP, data integrity, and safety standards
 
 Key Responsibilities
Laboratory Testing &amp; Analysis
<ul>
<li>Perform wet chemistry testing including IR, pH, TLC, solubility, and related analyses</li>
<li>Conduct HPLC testing and related instrument activities</li>
<li>Follow compendial methods (USP / EP / JP)</li>
<li>Execute testing using approved written procedures and SOPs</li>
</ul>
Validation &amp; Documentation
<ul>
<li>Draft and execute method validation protocols</li>
<li>Write validation and analytical reports</li>
<li>Perform peer review and technical review of analytical data, protocols, and reports</li>
<li>Maintain Good Documentation Practices (GDP) and Data Integrity compliance</li>
</ul>
Quality &amp; Investigation
<ul>
<li>Identify Out-of-Specification (OOS) results</li>
<li>Conduct root cause investigations with minimal guidance</li>
<li>Recommend and document corrective actions as required</li>
</ul>
Instrument &amp; Compliance Activities
<ul>
<li>Perform instrument, titrant verification, and calibration as scheduled</li>
<li>Support GMP, cGMP, ISO 9001/14001/45001 requirements</li>
<li>Maintain laboratory safety, housekeeping, and 5S practices</li>
</ul>
Collaboration &amp; Continuous Improvement
<ul>
<li>Work effectively within a team environment</li>
<li>Support process improvement, quality, and safety initiatives</li>
<li>Demonstrate company Core Values: Courage, Respect, Achievement, Integrity, Responsibility, Transparency</li>
</ul>
Required Qualifications
Education &amp; Experience
<ul>
<li>Bachelor's degree in Chemistry or Life Sciences + minimum 5 years of lab experience</li>
<li>OR</li>
<li>Associate degree in Chemistry or Life Sciences + minimum 10 years of non-academic lab experience</li>
</ul>
Technical Skills
<ul>
<li>Wet chemistry &amp; analytical testing</li>
<li>HPLC</li>
<li>Method validation</li>
<li>Compendial testing (USP/EP/JP)</li>
<li>GMP laboratory experience</li>
<li>Strong documentation and data review skills</li>
</ul>
Soft Skills
<ul>
<li>Strong planning, organization, and critical thinking</li>
<li>Ability to manage larger projects with minimal oversight</li>
<li>High attention to detail and proactive issue escalation</li>
</ul>
Self-driven and solution-oriented
 
Physical &amp; Safety Requirements
<ul>
<li>Ability to stand for long periods</li>
<li>Ability to lift up to 25 lbs</li>
<li>Exposure to chemicals requiring PPE</li>
<li>Compliance with OSHA and site safety standards</li>
</ul>
 
Pre-Employment Requirements
<ul>
<li>Background check</li>
<li>Drug &amp; alcohol screening</li>
<li>Pre/annual medical monitoring</li>
</ul>
 
About Trident: 
Trident Consulting is a premier IT staffing firm providing high-impact workforce solutions to Fortune 500 and mid-market clients. Since 2005, we've specialized in sourcing elite technology and engineering talent for contract, direct hire, and managed services roles. Our expertise spans cloud, AI/ML, cybersecurity, and data analytics, supported by a 3M+ candidate database and a 78% fill ratio. With a highly engaged leadership team and a reputation for delivering hard-to-fill, niche talent, we help organizations build agile, high-performing teams that drive innovation and business success.
 
Some of our recent awards include: 
Trailblazer Women Award 2025 by Consulate General of India in San Francisco
Ranked as the #1 Women Owned Business Enterprise in the large category by ITServe.
Received the TechServe Excellence award.
Consistently ranked in the Inc. 5000 list of fastest-growing private companies in America
Recognized in the SF Business Times as one of the Largest Bay Area BIPOC/Minority-Owned Businesses in 2022.

Chemistry Expert 2

<h3>Job Description</h3>
The Staff Scientist will prepare grant applications and other scientific communication materials on a wide range of genomic research topics. This role is deeply immersed in the science of NYGC and supports our research team in building and expanding a successful, independently-funded research base. They collaborate with diverse teams of students, postdoctoral fellows, and principal investigators, and relates scientific and strategic goals to individual grant opportunities and other research communications vehicles. Typical grants include individual investigator, multi-PI and research center grants.
 
Key Responsibilities
<ul>
<li>Takes a lead role in preparation and project management of individual and multi-investigator proposals;</li>
<li>Provides advice on grantsmanship, editorial support and standardized language for administrative sections;</li>
<li>Identifies opportunities for funding</li>
<li>Manages the scientific writing process, including proposal management, team-building and coordination; establishing timelines and deliverables;</li>
<li>Provides draft preparation, review and revision of grants and scientific writing.</li>
<li>Coordinates with and supports Sponsored Research staff to ensure timely, accurate application submission.</li>
<li>Edits manuscripts, fellowship applications, research progress reports, clinical research protocols and other research communications materials.</li>
<li>Interacts with lab members to independently develop new grant proposals.</li>
<li>Organizes small group meetings with lab members to review project progress, plan experiments, and integrate team data.</li>
<li>Assists in the design and planning of functional genomics and genetic perturbation experiments; and,</li>
<li>Assists in analysis and figure preparation of diverse types of data, including high-throughput sequencing, microscopy images, gel images, and schematic diagrams.</li>
</ul>
 
Key Responsibilities include (but are not limited to):
<ul>
<li>PhD in genetics, genomics, cancer biology, neuroscience or related discipline required;</li>
<li>5+ years research experience, including contributing to grant writing, required. NIH experience strongly desirable;</li>
<li>Exceptional written communication skills required to prepare and edit competitive grant applications, publications, administrative materials, and other research communications;</li>
<li>Ability to grasp complicated technical subjects, synthesize diverse lines of evidence and apply these abilities to technical writing required;</li>
<li>Experience handling the scientific writing and project management process for multi-investigator and institutional grant applications strongly preferred;</li>
<li>Experience with standard grant development concepts, practices, and procedures in a research environment preferred;</li>
<li>Applied statistics background required, to perform power calculations and develop quantitative metrics for genomic assays;</li>
<li>Ability to collaborate with diverse teams of investigators and administrative personnel required; and,</li>
<li>Strong project management skills and experience required.</li>
</ul>
 
Competencies
<ul>
<li>Technical and Professional Skills: Consistently demonstrates skills and knowledge relevant for current role; strives to expand the depth and breadth of technical and professional skills; works with a high level of integrity; exhibits focus and discipline; appropriately prioritizes, manages expectations, and delivers on commitments.</li>
<li>Collaborative &amp; Communicative: Models collaboration and teamwork; brings out the best in others; effectively works with all levels, internally and externally; respects and embraces diversity of perspective; communicates clearly and listens carefully; uses good judgment as to what to communicate and when to do so.</li>
<li>Adaptable &amp; Innovative: Adaptable and embraces change; develops new insights and pursues improvements and efficiency; fosters exchange of new ideas and willing to challenge the status quo; takes initiative and is solution-oriented; engages in work with passion and curiosity.</li>
</ul>
 
Salary
The salary range for this position is $62,000-78,000 per year. Base pay offered may vary depending on job-related knowledge, skills, and experience. In addition, NYGC offers a full range of medical, financial, and other benefits as well as generous time off.
 
About the New York Genome Center
The New York Genome Center (NYGC) is an independent, nonprofit, academic research organization dedicated to advancing genomic research. NYGC scientists and staff are furthering new approaches to diagnosing and treating neurological diseases and cancer through their unique capabilities in whole genome sequencing, RNA sequencing, state-of-the art analytics, and the development of genomic tools. NYGC concentrates specifically on disease-based research in the following areas: neuropsychiatric disease (autism, schizophrenia, bipolar); neurodegenerative disease (ALS, Alzheimer’s, Parkinson’s, Huntington’s), and cancer.
Located in Lower Manhattan, the New York Genome Center was founded by and remains closely affiliated with the leading academic medical centers and research universities in the New York region, engaging in research projects with and for these institutions. Essential to our collaborative work is an outstanding faculty, whose members typically hold a joint appointment at NYGC and a partner university. They support our scientific mission by conducting independent research in areas of mutual interest to us and the wider scientific community.
 
Equal Opportunity
We are committed to fostering a workplace environment that is welcoming and fair to all, ensuring that every employee has the opportunity to thrive. We believe that bringing together individuals with diverse backgrounds, experiences, and perspectives leads to greater collaboration, innovation, and discovery. Valuing and supporting each employee in reaching their full potential strengthens our organization and enhances our collective success. We recognize that creating an environment where all employees feel valued and included requires sustained effort and dedication from the entire organization.
The New York Genome Center is a VEVRAA Federal Contractor. All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of race, creed, color, gender, religion, national origin, sexual orientation, age, disability, genetic predisposition or carrier status, protected veteran or military status, domestic violence victim status, partnership status, caregiver status, alienage or citizenship status, marital status, or any other characteristic protected by applicable law. NYGC takes affirmative action in support of its policy to hire and advance in employment individuals who are protected veterans and individuals with disabilities. 
 
FLSA Status – Exempt
This position is eligible for visa sponsorship and relocation assistance.

Staff Scientist / Grant Writer, Sanjana Lab

<h3>Job Description</h3>
ARM Group is looking for a self-driven Senior Geotechnical Engineer who has a strong business acumen and embodies an ownership mentality. As a Senior Engineer, you will collaborate with a team of multi-disciplined engineers and scientists, project managers, CAD designers, and other staff to service our Geotechnical needs. This role will establish client relationships, define client needs, develop winning strategies, prepare proposals, and manage the development, design and permitting of a wide range of projects related, including: shallow foundations; deep foundations; retaining structures; karst hazards; mechanically stabilized earth (MSE) berms/walls; slope stability; ground improvement techniques; geotechnical support of shale gas projects and solid waste projects; and others. Experience with dam inspections, monitoring, rehab, and permitting is also desired.
 
Primary Responsibilities:
<ul>
<li>Manage and coordinate multiple projects simultaneously.</li>
<li>Maintain schedules, develop project timelines, coordinate with subcontractors, and manage people and materials to complete jobs on schedule and within budget guidelines.</li>
<li>Act as the direct point of contact in communication with clients and stakeholders.</li>
<li>Assess and mitigate project risks in advance of detailed engineering efforts.</li>
<li>Assist the ARM business development team, including the preparation of technical proposals.</li>
<li>Perform and/or check technical calculations and prepare project reports and specifications.</li>
<li>Prepare client communications, proposals, contract documents, etc. and consults with other internal partners as needed.</li>
<li>Monitor project work progress, adhere to the scope of work and communicate with key stakeholders including the project manager, client, and subcontractors.</li>
<li>Pro-actively recognize conditions and problems of non-routine nature and develop effective solutions.</li>
</ul>
 
Requirements
<ul>
<li>Bachelor’s degree in civil engineering is a minimum. Master’s degree in Geotechnical Engineering is preferred.</li>
<li>P.E. registration required.</li>
<li>5+ years of geotechnical experience.</li>
<li>Excellent communication and public speaking skills: articulate, assertive, and confident.</li>
<li>Strong organizational skills with proven ability to manage multiple, complex projects.</li>
<li>Creative thinker with effective teamwork skills.</li>
<li>Ambitious and eager to grow.</li>
<li>Detail-oriented and thorough.</li>
<li>Strong work ethic and self-motivated mentality.</li>
<li>Ability to communicate orally and in writing with key stakeholders.</li>
<li>Must have strong technical competency and analytical ability.</li>
<li>Must be able to work independently and collaborate with peers when appropriate.</li>
<li>Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the public.</li>
<li>Experience managing vendor and client payment terms to achieve positive cash flow.</li>
<li>Understanding of financial models and budget management.</li>
<li>Reasonably proficient in AutoCAD, MS Office Suite, and other industry-specific software.</li>
</ul>
 
Your Wellness, Our Priority: A Look at Our Benefits
We invest in our team's well-being and future through a comprehensive benefits package with a range of offerings designed to support you holistically. Our health and wellness offerings include two Health Insurance options (Traditional PPO and QHDHP with an HSA), vision and dental coverage, life insurance, disability protection, accident and critical illness coverage. To enhance your future financial security, we provide a 401(k) with company match, HSA/FSA accounts, and 529 college savings plans. Work-life balance is prioritized through our generous PTO starting at 15 days per year and 10 paid holidays per year, giving you ample time to rest, recharge, and attend to life outside the office. An Employee Assistance Program is provided to you and your household with resources to assist you in managing a variety of situations. We invest in your professional growth through our Tuition Reimbursement program and continuing education opportunities. After 6 months of employment, all team members become eligible for quarterly bonuses, providing additional avenues for financial growth. This robust package is designed to foster a workplace where you can thrive both personally and professionally, underscoring our dedication to your overall well-being and future success.

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