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Review Process Lead
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$55 an hour
Full-time
- This position acts as the interface with Regulatory Advertising and Promotion (RAP), Privacy, Health Care Compliance Officers (HCCOs), Law Department, study team members, suppliers, and other stakeholders involved in the development, management, and dissemination of patient and site-facing tactics.
- Skills; Patient recruitment, Veeva and clinical trials.
- At least 3 years of relevant experience in global patient recruitment, clinical trial execution with a pharmaceutical company, CRO, and/or healthcare facility/research site.
- Expertise in the areas of drug development, clinical trial operations, and strategic planning.
- Previous experience in clinical trial operations including the execution of study outreach, patient compliance and study support programs.
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