Job Description

A fast-growing dermatology office (Waterford and Livona) is looking for a Clinical Research Coordinator.

The Clinical Research Coordinator 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.

Job Tags

Full time,

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