Study Coordinator (6-12 Month Contract)

BioAgilytix • Durham, NC

1d • Onsite

About The Position

At BioAgilytix, we are passionate about premier science and the impact it has on our world. Our team of highly experienced scientists and professionals deliver tailored services for supporting new medicine breakthroughs with best-in-class bioanalytical services. We are tirelessly committed to our customers by being solution-oriented and deadline-driven. . . and we are growing. Our culture is fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You’ll gain experience with a variety of challenges all while you enable life-changing, life-saving therapeutics to the patients who need them.
We are seeking a Study Coordinator for a 6-12 month contract to support our Durham, NC laboratory. This role is ideal for candidates with experience working in a GxP-regulated environment who can quickly learn systems, evaluate processes, and ensure compliance with quality standards.
This position is on-site 5 days per week.
The ideal candidate has an acute attention to detail and who brings a collaborative mindset and a commitment to scientific quality. If you thrive in a fast-paced environment, approach challenges with curiosity and ownership, and are passionate about ensuring the highest caliber of data for our clients, you’ll feel right at home at BioAgilytix.

Requirements

• Bachelor’s degree in biochemistry, biotechnology, immunology, molecular biology, or related field with not less than one (1) years’ experience in a laboratory environment or related field; or
• Masters’ 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
• Experience working in a GxP environment preferred

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
• May support sample management activities
• May prepare Sample Analysis worklist
• Support Sample Analysis Plan generation
• Maintain CoA’s, CoT’s, and reagent records
• Assist in Quality review data submission for Sample Analysis Projects
• May support data table assembly for Sample Analysis Projects
• Provide information for Sample Analysis Reports
• May support providing information for Client Specific Metrics and Tracking
• Adhere to safety and compliance requirements
• Other duties as assigned

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 251-500 employees