Laboratory Research Associate
About The Position
The Clinical Laboratory Research Associate (CRA) will join our dedicated clinical laboratory team and be responsible for the analysis and data collection for clinical laboratory device trials. They will serve as a point of contact for multiple clinical trials and specimen procurements, while preparing and maintaining regulatory records, protocols, supply accountability, case report forms (CRFs), shipping records, de-identification and ID crosswalk. They will participate in site sponsor visits, trainings, and inspections. They will assist in assessing the feasibility of clinical study protocols, development of workflow procedures, and drafting of Institutional Review Board (IRB) submissions. They will maintain the quality and integrity of the clinical data through completion of eCRF database and on-site source verification records while working with sponsors to resolve queries and helps ensure all study deliverables are completed per study timelines. The CRA will manage all trial data files for studies and help train new/ ad hoc research staff on protocol requirements, source documentation, EDC system, case report form completion, and workflow.
Requirements
- Associate’s degree WITH at least 2 years of clinical laboratory or research experience
Nice To Haves
- Bachelor’s degree in scientific discipline or health care
Responsibilities
- Analysis and data collection for clinical laboratory device trials
- Serve as a point of contact for multiple clinical trials and specimen procurements
- Preparing and maintaining regulatory records, protocols, supply accountability, case report forms (CRFs), shipping records, de-identification and ID crosswalk
- Participate in site sponsor visits, trainings, and inspections
- Assist in assessing the feasibility of clinical study protocols, development of workflow procedures, and drafting of Institutional Review Board (IRB) submissions
- Maintain the quality and integrity of the clinical data through completion of eCRF database and on-site source verification records while working with sponsors to resolve queries and helps ensure all study deliverables are completed per study timelines
- Manage all trial data files for studies and help train new/ ad hoc research staff on protocol requirements, source documentation, EDC system, case report form completion, and workflow.
Benefits
- We offer medical, dental, and vision coverage starting the first of the month after hire for employees working 24+ hours/week.
- Additional perks include discounted childcare through Bright Horizons and voluntary benefits like pet insurance, legal services, and identity theft protection.
- We support your long-term wellness with a 403(b) retirement plan and company match, flexible spending accounts, access to financial advisors, and up to $400/year in wellness rewards.
- When life gets tough, we’re here with 24/7 EAP counseling, virtual mental health support, a food pantry, PTO donation program, and professional attire through the Classy Closet.
- With access to 100,000+ online courses, leadership programs, tuition reimbursement, clinical ladders, and internal mobility, we help you grow wherever your passion leads.
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What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Education Level
Associate degree
