The role involves managing all aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings
Job Summary
The role involves managing all aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings.
Candidates will serve as the primary point of contact for the project team and business unit while ensuring deliverables are met within the contract timeline.
Join a global team that values passion, innovation, and a commitment to scientific excellence where collaboration is part of the everyday experience.
Matching Summary
The role involves managing all aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings.
Salary
Not specified; Not specified; Not specified
Skills & Requirements
Must-have
Phase I clinical processes knowledge
FDA regulations and ICH GCP guidelines
IRB submission and informed consent creation
Risk register and mitigation plan development
Budgeting and fiscal management for studies
Vendor oversight and contract adherence
Nice-to-have
Strong consulting and liaison skills
Adaptability to changing study needs
Collaborative team environment experience
Commitment to scientific excellence
Effective multi-tasking abilities
Key Requirements
Bachelor's degree or equivalent qualification
2+ years of relevant clinical research experience
Knowledge of Phase I processes and clinical study operations