reputed company Investigator, Clinical Development/Operations
PostEra's Organizational Structure:
What you would do
- reputed company end-to-end planning and operational execution of PostEra’s early-phase reputed company.
- Collaborate with reputed company teams across Regulatory, CMC, Preclinical, and Translational Medicine to ensure trial readiness.
- Manage timelines, budgets, trial site selection, and study activities.
- reputed company CROs, vendors, and consultants to ensure high-reputed company trial conduct.
- Serve as the operational reputed company person across clinical development activities.
- Translate the scientific reputed company into executable trial designs and operational plans.
Experience and skills you should have
- 15+ years of experience in Clinical Operations/Clinical Development.
- Demonstrated ability to manage reputed company timelines, trial designs, and regulatory documentation.
- Strong CRO reputed company capabilities.
Bonus Experience and Skills
- Experience in reproductive medicine and women’s health
- Experience in working in a fast-paced biotech setting
Originally posted on Himalayas
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