Analytical Science Clinical Data Review Supervisor

Company Description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees with the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording your work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery of pharmacology, forensics, CDMO, advanced material sciences, and in the support of clinical studies.

If you’re looking for a rewarding career, a place to call home, apply with us today

Job Description

The Analytical Science Clinical Data Review Supervisor is responsible for supervising clinical laboratory data review activities, ensuring data integrity, regulatory compliance, and timely delivery of results. This role leads and develops QC data review teams while coordinating training, investigations, and process improvements to support high-quality analytical science operations.

Key Responsibilities

• Manage and coordinate training programs for laboratory and data review staff to ensure compliance with regulatory and procedural requirements.
• Coordinate and support the implementation of laboratory process and safety improvements.
• Review laboratory logbooks and records for completeness, accuracy, and regulatory compliance.
• Verify chain of custody integrity for all tested samples.
• Review audit trails to confirm actions were executed appropriately and within timelines defined by governing procedures.
• Partner with testing teams to resolve data discrepancies, corrections, and annotations to ensure compliance standards are met.
• Conduct laboratory investigations, including root cause analysis, and prepare clear, compliant investigation reports.
• Review and verify both paper and electronic laboratory data.
• Perform data review for Clinical Routine and Process Sciences testing, including compendial assays, ELISA, gel electrophoresis, and HPLC.
• Communicate routine deliverables, status updates, and findings to appropriate internal and client-facing teams.
• Utilize the Laboratory Information Management System (LIMS) to track samples, results, investigations, and performance metrics.

• Supervise direct reports, group leaders, and technical teams within a clinical laboratory environment.
• Promote and model the company’s vision, values, and culture of quality.
• Coordinate and participate in hiring, interviewing, and selection activities.
• Oversee staff scheduling, workload distribution, and onboarding of new hires.
• Manage overtime and weekend schedules to meet operational and client needs.
• Develop and implement team-building initiatives to support engagement and performance.
• Apply Lean and continuous improvement principles to optimize data review workflows.
• Supervise daily operations of the Quality Control (QC) clinical data review team.
• Coach, mentor, and support group leaders while monitoring productivity and quality performance.
• Support ongoing professional development and career growth of team members and group leaders.

Qualifications

• Bachelor’s degree in Chemistry, Life Sciences, Engineering, or a related scientific discipline.
• Minimum of 3 years leading dynamic teams in technical or laboratory settings, with a strong emphasis on team development, coaching, and performance management.
• At least 3 years of hands-on laboratory experience; prior work in a GMP-regulated environment is strongly preferred.
• Experience with HPLC, MCE, and/or ELISA data strongly preferred
• Experience with chromatography processing and review of logbooks, electronic lab notebooks, and LIMS
• Demonstrated experience managing day-to-day lab operations, including workflow optimization, equipment oversight, and compliance with safety and quality standards.
• Proven ability to serve as a liaison between internal teams and external clients, ensuring effective communication, timely project execution, and high client satisfaction.
• Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

What to Expect in the Hiring Process:

• 10-15 Minute Phone Interview with Regional Recruiter
• 45-60 Minute Virtual Interview with Manager and/or Group Leader
• 30 Minute In-Person Onsite Meeting with the Team

This is a full-time, 100% onsite position based on a first-shift schedule (Monday–Friday, 8:30am–4:30pm), with overtime required as needed. Candidates located within a commutable distance to Rensselaer, New York, are strongly encouraged to apply.

What We Offer:

• Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Yearly goal-based bonus & eligibility for merit-based increases
• Hourly compensation is between $38.00 - $41.00 per hour, depending on education and experience

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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