Job Information
System One Clinical Research Coordinator (CRC) in Rochester Hills, Michigan
Title: Clinical Research Coordinator
Location: Rochester Hills, MI
Schedule: 8a-5p
Type: Contract, 6 months
Start Date: ASAP
Joule is currently looking to hire a Clinical Research Coordinators at a Rochester Hills, MI site. You must possess at least 2 years of experience in coordinating clinical 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
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.