Responsible for the clinical science aspects relative to the study team, Study Leadership Team (SLT) or project team and may lead a clinical study or other project
Job Summary
Responsible for the clinical science aspects relative to the study team, Study Leadership Team (SLT) or project team and may lead a clinical study or other project.
Contribute to the clinical science aspects of the CDP strategy and clinical documentation, representing the CDP on appropriate sub-teams and forums.
Perform responsibilities independently, with interactions with external stakeholders, e.g. investigators, Therapy Area Experts (TAEs) and vendors.
Matching Summary
Responsible for the clinical science aspects relative to the study team, Study Leadership Team (SLT) or project team and may lead a clinical study or other project.
Salary
Base: $141,000 - $262,000; Bonus/Equity: Discretionary annual bonus may be available; Benefits: Not specified
Skills & Requirements
Must-have
Late stage R&D drug development
Clinical trial execution
Medical data reviews
Protocol medical reviews
Cross-functional collaboration
Nice-to-have
External stakeholder interactions
Health Authority interactions
Clinical outcome trials
Therapeutic area expertise
Key Requirements
Advanced Clinical/Science Degree
3+ years clinical development industry experience
3+ years experience designing and conducting medical data reviews
Knowledge of governing laws, regulations, guidelines and Roche SOPs