PMV Pharma is hiring a
Senior Director Clinical Scientist

Summary

Join our team as the Senior Director, Clinical Scientist, Oncology, leading scientific planning and execution of clinical trials, overseeing design, conduct, analysis, and reporting, while ensuring alignment with regulatory requirements and corporate objectives.

Requirements

• MD, PhD, PharmD, MS, or equivalent degree in life sciences required
• Minimum of 8 years of experience in clinical science, clinical research, or equivalent; with required experience in Oncology
• Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols
• Strong understanding of regulatory requirements and guidelines for clinical trials (e.g., GCP, ICH, FDA)
• Experience working in a matrix management and cross functional team environment
• Ability to interact externally and internally to support scientific and business strategy
• Excellent analytical and organizational skills
• Must possess excellent oral and written communication and presentation skills
• Demonstrable abilities to effectively communicate project direction and status to varying organizational levels, including leadership teams, executives and steering committees. Able to distill complex matters into a clear business case and roadmap for execution

Responsibilities

• Serve as the lead clinical scientist on clinical trials, providing scientific and strategic direction
• Oversee the design, conduct, analysis and reporting of clinical trials in accordance with GCP and ICH guidelines
• Perform site-facing activities such as training and responding to clinical inquiries
• Review development of site and CRA training materials and presentation at Site Initiation Visits and Investigator meetings and support on Study committee (e.g., Safety Review Committee) activities
• Conduct activities related to data generation and validation, and clinical data review/query resolution
• Work closely with cross-functional teams, including Medical Affairs, Clinical Operations, Regulatory Affairs, and Research, to ensure the successful progression of our clinical programs
• Collaborate with principal investigators, key opinion leaders, and clinical trial sites to ensure robust study design and execution
• Lead the monitoring team in the review and interpretation of clinical data and protocol deviations
• Contribute to the preparation of clinical study reports, regulatory submissions, and publications
• Present clinical trial data and findings to internal and external stakeholders, including scientific advisory boards and regulatory agencies
• Reviews competitive landscape and supports the identification of business development opportunities