
Study Coordinator
1w1 week agoBioAgilytix
Durham, US · Contract · $50,000 – $70,000
About this role
At BioAgilytix, we are passionate about premier science and the impact it has on our world. Our team of highly experienced scientists delivers tailored services for supporting new medicine breakthroughs with best-in-class bioanalytical services. We are seeking a Study Coordinator for a 6-12 month contract to support our Durham laboratory.
This role supports maintaining accurate study records, tracking project samples received, tested, and reported, and tracking Assay QCs during Project Sample Analysis. Additional duties include supporting project inventory, study start-up and close-out activities, and sample management. Assist in quality review of data submissions and provide information for Sample Analysis Reports.
The position is on-site 5 days per week in a primarily office environment at our Durham location. Ideal candidates bring acute attention to detail, a collaborative mindset, and thrive in a fast-paced, fun culture. Frequent supervision is provided with infrequent discretionary authority.
Work across numerous clients and drug modalities to develop rapidly while gaining experience with a variety of challenges. Enable life-changing, life-saving therapeutics for patients in need. Approach challenges with curiosity, ownership, and passion for scientific quality.
Requirements
- Bachelor’s degree in biochemistry, biotechnology, immunology, molecular biology, or related field with at least one year’s experience in a laboratory environment
- Or Master’s degree in biochemistry, biotechnology, immunology, molecular biology, or related field
- Knowledge base in science with the relevant regulations for our industry
- Excellent oral and written communication skills
- High level of proficiency in Microsoft Office (Word, Excel, Outlook)
- Acute attention to detail
- Ability to work effectively within team to meet objectives under time constraints
- Strong organizational and project administration skills
Responsibilities
- Maintain accurate study records, including sample and study documentation received
- Track project samples received, tested, and reported
- Track Assay QCs and testing performed during Project Sample Analysis
- Support project inventory and related activities
- Support start up and end of study activities
- Support sample management activities
- Prepare Sample Analysis worklist
- Maintain CoA’s, CoT’s, and reagent records
Benefits
- Fast-paced, fun and never boring culture
- Work across numerous clients and drug modalities
- Enable life-changing, life-saving therapeutics
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