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Clinical Research Coordinator/Medical Assistant
A fast-growing dermatology office (Waterford and Livona) is looking for a Clinical Research Coordinator/Medical Assistant.
The Clinical Research Coordinator/Medical Assistant is responsible for coordinating all clinical studies in the office. This candidate assists with Phase 2, Phase 3, and Phase 4 clinical research studies and registry studies. The ideal candidate is a hard-working - self-starter, that is punctual, and a team player.
The position encompasses various job tasks, which are listed below:
The Clinical Research Coordinator/Medical Assistant is responsible for coordinating all clinical studies in the office. This candidate assists with Phase 2, Phase 3, and Phase 4 clinical research studies and registry studies. The ideal candidate is a hard-working - self-starter, that is punctual, and a team player.
The position encompasses various job tasks, which are listed below:
Patient Care management:
- HIPPA compliance.
- Administer medications.
- Process samples.
- Administer EKG, blood draws, and blood pressure.
- Patient scheduling.
- Patient phone calls.
- Obtaining needed medical records.
Data Management:
- Data entry EDC (examples red cap, trial master, RAVE).
- Use of various data entry research portals.
- Compliance with different data storage requirements.
Certifications and Sponsor Training:
- Good clinical practice certification
- Dangerous goods certification.
- Biohazard materials certification.
- Infectious diseases certification.
- Proper organization of regulatory documents.
Required Experience:
- Microsoft Office experience is a MUST.
- Attention to detail; excellent written and verbal communication is a MUST.
Preferred Experience:
- Pharmacy experience.
- Medical terminology.
- Clinical patient care.
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