Scientific Affairs Analyst in United States at Jobgether
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Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Scientific Affairs Analyst based in United States.
This role sits at the intersection of clinical laboratory science and clinical trial operations, supporting the scientific and operational backbone of pre-award study activities. You will analyze clinical trial protocols to determine testing requirements and ensure accurate, timely responses for proposals and RFPs.
You will act as a key liaison between laboratory operations, R&D teams, sales, and external referral laboratories.
The position plays a critical role in translating scientific and technical requirements into executable laboratory workflows for ongoing and upcoming clinical studies.
You will contribute directly to study feasibility, pricing accuracy, and testing coordination across multiple stakeholders.
The environment is highly collaborative, fast-paced, and detail-driven, requiring strong scientific judgment and communication skills.
Your work will help ensure that clinical trial testing is properly scoped, supported, and executed across internal and external partners.
- Review clinical trial protocols to identify testing requirements and determine appropriate laboratory capabilities for study support.
- Coordinate with internal R&D, laboratory operations, and external referral labs to ensure accurate and timely study setup and execution.
- Prepare and review pricing and proposal documentation, identifying discrepancies and ensuring scientific accuracy.
- Serve as a liaison between laboratory teams, sales, and project management to support RFPs, RFIs, and ongoing study needs.
- Track and document referral testing information throughout active trials, including contracting and operational updates.
- Monitor study lifecycle issues, escalate risks to leadership, and support corrective action implementation when needed.
- Contribute to process improvements aimed at increasing efficiency, reducing costs, and optimizing laboratory operations.
- Bachelor’s degree in a scientific discipline or equivalent experience (e.g., 3+ years as a clinical laboratory scientist).
- At least 2 years of laboratory experience and 1 year of clinical trials exposure.
- Strong understanding of clinical laboratory processes and generalist lab workflows.
- Excellent communication and interpersonal skills for cross-functional and external collaboration.
- Strong organizational and time management abilities with experience handling multiple concurrent projects.
- Proficiency in Microsoft Office and standard business documentation tools.
- Ability to work independently while contributing effectively in team environments.
- MT (ASCP) certification is preferred but not required.
- Competitive annual salary ranging from approximately $70,000 to $90,000.
- Opportunity to work at the interface of clinical science, laboratory operations, and clinical trial development.
- Exposure to cross-functional collaboration with R&D, sales, project management, and external research partners.
- Structured full-time schedule (Monday to Friday, 40 hours per week).
- Professional growth opportunities in clinical trials and scientific operations.
- Inclusive workplace environment with equal opportunity employment practices.
- Eligibility for additional compensation components depending on role structure and location.