Remote Associate Director — Clinical Science Leader

Ladders; United States; Remote; USD 150.000 - 195.000; Vollzeit

Benefits dieser Stelle

Premium health offerings for employees

Wellness programs

Life insurance and disability coverage

Retirement plans with employer match

Generous paid time off

Zusammenfassung

Ladders is seeking an Associate Director, Clinical Scientist to join our client’s leadership team in Pharmaceuticals & Biotech. This role shapes clinical science strategy across study planning, protocol design, and study execution in a highly regulated development environment.

The Associate Director will partner with clinical operations, regulatory, and cross-functional teams to generate clear, decision-ready insights from complex trial data, advancing programs through strong documentation and

Qualifikationen

• PhD, PharmD, or MD in a related life science discipline is required.
• 4+ years in the pharmaceutical industry; rare disease experience preferred.
• Experience supporting clinical trials and studies; human pharmacology studies preferred.
• Ability to review and present complex scientific and clinical data effectively.

Aufgaben

• Lead clinical science components of study plans and protocol design.
• Review and summarize clinical trial safety and efficacy data for team discussions.
• Coordinate clinical science activities and maintain organized documentation.
• Support study conduct in compliance with protocols and GCP regulations.
• Prepare and review clinical reports and presentations with cross-functional teams.
• Contribute to regulatory submissions and scientific documents.
• Build relationships with external partners and represent the clinical science team.

Kenntnisse

Clinical data interpretation

Presenting complex data

Ausbildung

PhD, PharmD, or MD in life sciences

Jobbeschreibung

Ladders is seeking an Associate Director, Clinical Scientist to join our client’s leadership team in Pharmaceuticals & Biotech. This role shapes clinical science strategy across study planning, protocol design, and study execution in a highly regulated development environment.

The Associate Director will partner with clinical operations, regulatory, and cross-functional teams to generate clear, decision-ready insights from complex trial data, advancing programs through strong documentation and