Clinical Research Coordinator (CRC)

Title: Clinical Research Coordinator - Must have Vaccine experience
Location: Detroit Metro - Farmington Hills, Rochester, Clarkston
Schedule: 8a-5p
Type: Contract, 4 months
Start Date: ASAP

Joule is currently looking to hire 6 Clinical Research Coordinators to work in any of the 3 locations listed above. You must possess at least 2 years of experience in research and you must have experience working on Vaccine trials.

Role & Responsibilities:

• Conduct and manage all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
• Complete all relevant required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner.
• Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up.
• Ensure good documentation practices are applied by all team members when collecting, maintaining and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
• Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products.

Requirements & Skills:

• Bachelor's degree and 2 years relevant experience in the life science industry OR
• Associate's degree with 4 years relevant experience in the life science industry OR
• High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year Clinical Research Coordinator experience
• Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
• Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, processing/shipping lab specimens
• Proficient ability to work independently, plan and prioritize with minimal guidance
• Excellent attention to detail, organization, and communication with varied stakeholders
• Ability to work as a team player with the ability to adapt to changing schedules and assignments
• Ability to travel regionally or nationally if required