Specimen Processor
About The Position
Join Pharmaron's Clinical Research team as a Specimen Processor and play an important role in supporting the accurate processing, documentation, and storage of clinical trial specimens. You'll work in a fast-paced research environment where precision, quality, and attention to detail are essential to ensuring samples are handled according to study protocols and laboratory requirements. This is an excellent opportunity for a laboratory or phlebotomy professional looking to build or expand their experience in clinical research while gaining hands-on exposure to pharmacokinetic (PK) specimen processing and clinical trial operations.
Requirements
- High school diploma or equivalent required
- 1+ years of experience in a laboratory, specimen processing, phlebotomy, clinical research, or related healthcare environment.
- Strong attention to detail with the ability to accurately follow study protocols, laboratory manuals, and SOPs.
- Strong organizational and documentation skills with a commitment to data and specimen accuracy.
- Effective written and verbal communication skills.
- Ability to manage multiple priorities and work effectively in a fast-paced, quality-driven environment.
- Ability to work collaboratively as part of a clinical research team.
Nice To Haves
- additional education or training in laboratory science, phlebotomy, medical assisting, or a related field preferred.
Responsibilities
- Receive, process, centrifuge, aliquot, label, and store clinical research specimens according to study protocols and protocol-specific laboratory manuals.
- Accurately document each stage of PK specimen processing, including applicable centrifugation, processing, and storage times.
- Prepare and accurately label PK cryovials and other specimen containers prior to processing.
- Organize, track, and maintain PK specimens according to study-specific requirements.
- Verify specimen information and documentation for accuracy, completeness, and protocol compliance.
- Maintain appropriate specimen storage conditions and support specimen inventory activities.
- Follow study protocols, SOPs, Good Clinical Practice (GCP) requirements, and applicable laboratory quality standards.
- Identify and communicate specimen discrepancies or processing issues to the appropriate team members.
- Maintain organized and clean specimen processing areas and ensure required supplies are readily available.
- Collaborate with clinical research, laboratory, and operational teams to support timely and accurate specimen processing.
Benefits
- Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
- 401(k) Retirement Plan with generous employer matching
- Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
- Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
- 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
- Employee Assistance Program (EAP), mental health resources, and wellness programs
- Family-friendly benefits, including fertility support and maternity resources
- Professional development and career growth opportunities within a leading global CRO/CDMO
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
