```Duties```
- Oversee and coordinate clinical research studies in accordance with GCP and FDA regulations
- Manage data collection, entry, and analysis processes
- Supervise research staff involved in the studies
- Ensure compliance with protocols, regulatory requirements, and ethical standards
- Conduct clinical laboratory procedures as needed
- Review and maintain documentation for accuracy and completeness
- Collaborate with investigators and healthcare professionals to facilitate research activities
```Qualifications```
- Bachelor's degree in a related field such as healthcare or life sciences
- Proficiency in medical terminology and clinical research practices
- Experience in supervising staff and managing clinical research projects
- Knowledge of compliance management and FDA regulations
- Experience in FDA approved clinical trials (2+ years preferred)
- Strong skills in data management and documentation review
-Blood Draw experience (preferred)
Job Type: Full-time
Pay: $23.71 - $25.85 per hour
Benefits:
Schedule:
- 8 hour shift
- Monday to Friday
Ability to Relocate:
- Bloomfield Hills, MI 48302: Relocate before starting work (Required)
Work Location: In person
