Clinical Research Coordinator/Medical Assistant

About the Job 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: 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.