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- Drives the processes for assigned protocol registration activity, resulting in timely, high-quality information posted on clinical trial registries and EU PAS)
- Liaises with clinical team reviewers (Global Trial Managers, Operations Leads, Statisticians, Clinical Trial Physicians, Clinical Scientists, Development Leads, Patent Attorneys) and other stakeholders on all assigned trials to ensure trial registrations are accurate, consistent with the protocol and reported in adherence to NIH guidelines
- Provides maintenance support to CT Registration Lead for assigned records, to ensure the accuracy of information disclosed on
- Submits registration updates to on behalf of clinical team, within global regulatory timelines
- Maintains study trackers and ensures they are up to date every week
- Educates stakeholders, as needed, on NIH detailed review criteria for registrations as well as the purpose and format of patient-friendly fields in the protocol registration form
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Clinical Trial Registration Specialist - Lawrenceville, United States - ASK Staffing
Description
"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment".Job Title: Clinical Trial Registration Specialist
Location: Lawrenceville, NJ Remote)
Duration: 12 months
Pay rate:
$ / hour on W2
Job Description:
Hybrid - 50% onsite
Required Education:
B.S, M.S., or Ph.D...Pharm.D
ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.
