Vice President, Clinical Development - Biotech Leader

Green Life Science; Northern (KY); Hybrid; USD 250,000 - 420,000; Full time

Job summary

Green Life Science is seeking a Vice President of Clinical Development for the USA. Lead clinical development across programmes from early stages through registration and post-marketing activities, collaborating with internal teams, regulators, investigators, and patient groups to advance therapies for serious diseases.

You will oversee medical monitoring, safety oversight, and regulatory interactions with FDA/EMA; contribute to publications and medical affairs; and drive patient recruitment

Qualifications

• MD degree required.
• Minimum 10 years of clinical development experience in biopharma.
• Proven track record with regulatory submissions and approvals.
• Strong knowledge of FDA/EMA regulations, GCP, and ICH guidelines.

Responsibilities

• Provide strategic and medical leadership across programmes from development through registration and post-marketing.
• Oversee clinical development plans, protocols, and regulatory documentation.
• Ensure safety monitoring, eligibility reviews, adverse events reporting, and pharmacovigilance.
• Represent the company with FDA, EMA, and other authorities.
• Collaborate with Clinical Operations and external partners on trial execution and oversight.
• Engage investigators and advocacy groups to support study design and interpretation of results.
• Support patient recruitment and engagement strategies with study sites.
• Contribute to publications and medical affairs activities.

Skills

MD degree

Clinical development leadership

Regulatory submissions

FDA/EMA knowledge

Cross-functional collaboration

Written & verbal communication

Education

MD degree

Job description

Green Life Science is seeking a Vice President of Clinical Development for the USA. Lead clinical development across programmes from early stages through registration and post-marketing activities, collaborating with internal teams, regulators, investigators, and patient groups to advance therapies for serious diseases.

You will oversee medical monitoring, safety oversight, and regulatory interactions with FDA/EMA; contribute to publications and medical affairs; and drive patient recruitment