Senior Clinical Project Manager
New
O
OraOphthalmic Clinical Research
Remote - USFull-TimeSenior
Salary not disclosed
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Job Details
- Experience
- At least 7 years of clinical trial experience, including a minimum of 3 years of clinical project management experience
- Required Skills
- GCPMicrosoft ExcelPowerPoint
Requirements
- Bachelor’s degree in Life Science or equivalent professional experience.
- At least 7 years of clinical trial experience.
- Minimum of 3 years of clinical project management experience.
- Demonstrated expertise in applicable regulatory requirements and Good Clinical Practice (GCP).
- Experience with Veeva TMF and CTMS systems.
- Proficiency with Excel and PowerPoint.
- Strong vendor management skills.
- Ability to plan and manage project risks and operational outcomes.
- Effective organizational and communication skills.
- Ability to travel up to 15% (mainly domestic, overnight).
Responsibilities
- Manage cross-functional project teams to deliver high-quality clinical trials in compliance with regulations and SOPs.
- Initiate, plan, execute, control, close, and resource clinical trial projects.
- Coordinate interdepartmental groups including stats, data management, safety, manufacturing, and regulatory.
- Create and maintain project timelines, project plans, and communication plans.
- Perform weekly budget and progress reviews for each study.
- Review study metrics, protocols, source documents, and CRFs.
- Manage and coordinate all vendors such as central labs and reading centers.
- Represent the company at professional meetings and participate in bid defenses.
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