Medical Director-

Vivid Resourcing; United States; Remote; USD 200,000 - 300,000; Full time

Benefits offered by this job

Comprehensive benefits package

Work-life balance

Fully remote work

Job summary

A collaborative CRO is seeking a remote Medical Director to provide expertise across clinical programs. The role involves serving as a medical advisor, ensuring protocol integrity, and overseeing safety data reviews. Candidates should possess an MD, 5+ years of clinical experience, and strong regulatory knowledge. Competitive salary and comprehensive benefits offered.

Qualifications

• 5+ years of Clinical experience (post-residency) as a Physician.
• 2+ years in clinical development within pharma, biotech, or CRO environments.
• Experience/knowledge in Regulatory affairs with IND & NDA submissions is a plus.

Responsibilities

• Serve as medical and scientific advisor on assigned clinical programs.
• Oversee medical review of safety data, including AEs and SAEs.
• Provide clinical input on key documents such as protocols and reports.

Skills

Clinical experience

Regulatory guidelines knowledge

Communication skills

Ability to manage priorities

Education

MD (or equivalent)

Job description

Get AI-powered advice on this job and more exclusive features.

This range is provided by Vivid Resourcing. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$200,000.00/yr - $300,000.00/yr

Medical Director – (Remote, U.S.)

An opportunity to join a collaborative, science-driven CRO that values innovation, curiosity, and meaningful impact in clinical research. We’re seeking a Medical Director to provide expertise in medical, clinical and scientific fields across multiple therapeutic areas, contributing to the design, oversight, and interpretation of clinical programs from early development through regulatory submission.

Key Responsibilities

• Serve as medical and scientific advisor on assigned clinical programs.
• Ensure medical and ethical integrity in protocol design, study conduct, and data evaluation.
• Oversee medical review of safety data, including AEs, SAEs, and patient narratives.
• Provide clinical input on key documents such as protocols, investigator brochures, and clinical study reports (CSR).
• Partner with cross-functional teams to deliver high-quality outcomes for sponsors and stakeholders.
• Contribute to business development by supporting proposals, budgets, and sponsor meetings.

Qualifications

• MD (or equivalent) with an active or prior medical license.
• 5+ years of Clinical experience (post-residency) as a Physician.
• 2+ years in clinical development within pharma, biotech, or CRO environments.
• Strong grasp of general medicine, clinical trial methodology, and regulatory guidelines (ICH, GCP).
• Experience/knowledge in Regulatory affairs with IND & NDA submissions, CSRs etc. is a plus
• Proven ability to manage priorities, communicate effectively, and lead in a matrix environment.

Offer

• Competitive salary ($200k-$300k)
• Comprehensive benefits package for all benefit-eligible employees, which includes medical, vision, dental, HSA, FSA, EAP, life & disability insurance and 401(k).
• Encourages a work-life balance to allow employees to work fully remote.

If you're interested, please don't hesitate to apply or message me: [e-mail]