Medical Director

Atrio Search; United States; Remote; USD 150,000 - 200,000; Full time

Job summary

A leading executive search firm is seeking an experienced Medical Director for a remote position in the United States. The role includes providing medical and scientific leadership for clinical trials, ensuring patient safety, and regulatory compliance. Candidates must hold an MD or equivalent and have over 5 years of experience in clinical research or drug development. Strong knowledge of ICH-GCP regulations and excellent communication skills are required. If you're interested, please reach out via email for a confidential discussion.

Qualifications

• 5+ years in clinical research or drug development.
• Strong knowledge of ICH-GCP and global regulations.

Responsibilities

• Serve as medical monitor for clinical trials.
• Review and approve protocols, informed consent forms, and safety reports.
• Oversee adverse event evaluation and safety management.
• Provide medical input for study design and regulatory submissions.
• Collaborate with cross-functional teams and participate in investigator meetings.
• Support business development with medical expertise.

Skills

Excellent communication

Decision-making

Education

MD or equivalent

Job description

Direct message the job poster from Atrio Search

Executive Search Consultant – CDMO & CRO

Medical Director – CRO – United States (Remote)

Overview:

Provide medical and scientific leadership for clinical trials, ensuring patient safety, regulatory compliance, and high‑quality data. Act as the primary medical expert for assigned projects and support sponsors in study design and execution.

Key Responsibilities

• Serve as medical monitor for clinical trials.
• Review and approve protocols, informed consent forms, and safety reports.
• Oversee adverse event evaluation and safety management.
• Provide medical input for study design and regulatory submissions.
• Collaborate with cross‑functional teams and participate in investigator meetings.
• Support business development with medical expertise.

Qualifications

• MD or equivalent.
• 5+ years in clinical research or drug development.
• Strong knowledge of ICH‑GCP and global regulations.
• Excellent communication and decision‑making skills.

If interested, please reach out here or via email for a confidential chat – [e-mail].

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