Clinical Project Manager overseeing planning, execution, and delivery of clinical studies. Ensuring compliance and collaboration across teams in a remote setting.
About the role
- Senior Scientist leading clinical trials and scientific execution for a multinational pharmaceutical company. Guiding cross-functional collaboration and contributing to clinical protocol development while interpreting clinical data.
Responsibilities
- Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s)
- Serving as the lead clinical scientist on the clinical trial team
- Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director
- Collaborating cross-functionally in the development of Protocol and related study materials
- Ensuring CRF design supports data collection in alignment with the protocol in collaboration with Data Management/Programming
- Providing tactical/scientific mentorship to other clinical scientists
Requirements
- Bachelor’s degree + 5 years of pharmaceutical, clinical drug development, project management and or medical field experience OR Master’s degree + 3 years of pharmaceutical, clinical drug development, project management and/or medical field experience OR PhD / PharmD
- Demonstrated ability to drive and manage scientific activities on clinical protocols
- Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions
- Solid knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
- Ability to manage multiple competing priorities with good planning, time management and prioritization skills
- Must be proficient in English
Benefits
- medical, dental, vision healthcare and other insurance benefits (for employee and family)
- retirement benefits, including 401(k)
- paid holidays, vacation, and compassionate and sick days
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