Director, Clinical Development / Medical Monitor

Cpl Life Sciences US; United States; Remote; USD 100,000 - 125,000; Full time

Job summary

An established industry player is seeking a Director of Clinical Development / Medical Monitor to lead critical late-phase clinical trials in cardiology and metabolic diseases. This role offers the opportunity to make a significant impact in a rapidly growing biotech firm with a robust pipeline and a commitment to patient safety and data integrity. With a strong emphasis on collaboration and leadership, you will guide cross-functional teams and ensure adherence to medical protocols and regulatory standards. If you have a proven track record in clinical development and are ready to take the next step in your career, this is an exciting opportunity to join a team at the forefront of medical innovation.

Qualifications

• 5-10 Jahre Erfahrung in der klinischen Entwicklung und medizinischen Überwachung.
• Starker Hintergrund in Kardiologie, Nieren- oder Stoffwechselkrankheiten.

Responsibilities

• Leitung der medizinischen Aspekte von Phase 2 und 3 klinischen Studien.
• Sicherstellung der Patientensicherheit und Datenintegrität während der Studien.

Skills

Clinical Development

Medical Monitoring

Patient Safety

Data Integrity

Trial Design

Job description

Director, Clinical Development / Medical Monitor

Position: Director, Clinical Development / Medical Monitor

Location: Remote

I’m currently partnered with a rapidly growing biotech company specializing in cardiology, renal, and metabolic diseases. With a robust pipeline and multiple ongoing Phase 2 and 3 clinical trials, the company is making significant strides — their share price has nearly tripled in recent months, underscoring their momentum and success in the space.

They are now seeking a Director of Clinical Development / Medical Monitor with a minimum of 5 years’ experience to support the execution of their late-phase clinical trials.

Key Responsibilities:

• Lead and oversee the medical aspects of Phase 2 and 3 clinical trials
• Ensure patient safety and data integrity throughout the studies
• Provide expert medical input into trial design, conduct, and analysis
• Ensure adherence to medical protocols and regulatory standards
• Offer guidance and leadership to cross-functional study teams

Requirements:

• 5–10 years of experience in clinical development and medical monitoring
• Strong background in cardiology, renal, hypertension, or metabolic diseases (preferred)
• Proven ability to support and oversee Phase 2 and 3 clinical trials

Seniority level: Director

Employment type: Full-time

Job function: Management

Industries: Biotechnology Research and Pharmaceutical Manufacturing