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ConvaTec Group is seeking a Senior Clinical Study Manager to oversee the planning and execution of clinical trials, ensuring compliance with regulations and organizational goals. The ideal candidate will have at least five years of experience in managing clinical trials, particularly in the medical device industry, and will be responsible for mentoring junior team members.
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Job Summary
The Senior Clinical Study Manager oversees the planning, execution, and completion of clinical trials, leading teams and managing budgets to align with organizational goals.
Key responsibilities include managing study efficiency, analyzing risks, coordinating documentation, motivating teams, and ensuring compliance with ICH GCP guidelines and company SOPs.
The role requires extensive experience in independently managing clinical trials, a comprehensive understanding of investigative site capabilities, and advanced knowledge of federal regulations governing research.
Matching Summary
Match Score: 75
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ConvaTec Group is seeking a Senior Clinical Study Manager to oversee the planning and execution of clinical trials, ensuring compliance with regulations and organizational goals. The ideal candidate will have at least five years of experience in managing clinical trials, particularly in the medical device industry, and will be responsible for mentoring junior team members.
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Skills & Requirements
Must-have
manage clinical studies
adherence to project timelines and budget
manage clinical study risks
coordinate clinical study documentation
manage multi-disciplinary clinical study team
manage 3rd party clinical monitoring vendors
manage project budgets
ensure compliance with regulations
drive performance, quality, timelines, and relationships
Nice-to-have
mentoring junior team members
fostering a collaborative environment
build solid professional relationships with KOLs
Key Requirements
Minimum of 5 years independently managing clinical trials