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Company | Akorbi |
Address | South San Francisco, CA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Translation and Localization |
Expires | 2023-07-06 |
Posted at | 10 months ago |
Project Manager- Clinical Trials
- Maintain and communicate timelines, and lead cross-functional project planning meetings.
- Coordinate between Devices TPM and engineers, Clinical Supply, Data management, and various other teams to ensure on time launch and successful execution.
- Work closely with cross-functional teams to lead planning and execution of clinical studies and deploy Study Watch to support our external partners or our internal product development studies.
- Proven ability to manage complex projects involving multiple stakeholders, and in a fast pace environment.
- Exceptional organizational, documentation and general program management skills in a clinical trial setting, including stakeholder management with medical personnel and scientific research colleagues; excellent communication skills, with experience communication to executives
- 3-5 years of experience working in project management or similar discipline.
- Bachelor's degree or equivalent practical experience.
- Knowledge and experience of clinical trials.
- Ability to multi-task and organize different inputs to improve operational efficiency and efficacy.
- Ability to improvise, work efficiently and respond quickly to changes and a dynamic work-flow.
- Establish solid relationships with cross-functional teams.
- PMP certification
- Strong problem-solving and analytical skills, and ability to handle ambiguity and create order out of it
- Strong working knowledge of project management tools such as spreadsheets, docs, and project tracking software.
- Strong interpersonal skills with sensitivity to changing personalities and priorities.
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