In-House Clinical Research Associate
New
4
4DMTBiotechnology
Remote, United StatesContractMiddle
Salary60 - 70 USD per hour
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Job Details
- Experience
- Minimum of 1-2 years of experience supporting clinical trials
- Required Skills
- Microsoft Office
Requirements
- B.A. or B.S. degree.
- Minimum of 1-2 years of experience supporting clinical trials in a sponsor or CRO environment.
- Working knowledge of clinical trial operations and ICH GCP guidelines.
- Experience with TMF/eTMF systems (Veeva Vault preferred).
- Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
- Strong organizational skills and attention to detail.
- Ability to manage multiple priorities and meet deadlines.
- Strong interpersonal skills and ability to collaborate effectively with cross-functional teams.
- Experience supporting Phase 3 clinical trials (preferred).
- Ophthalmology experience (preferred).
- Willingness to travel as trial needs demand (<5% anticipated).
Responsibilities
- Support study execution across start-up, conduct, and close-out phases.
- Serve as a primary point of contact for assigned clinical sites and CRO field CRAs.
- Support oversight of CRO monitoring activities and review monitoring visit reports.
- Maintain tracking tools for site activation, subject enrollment, and essential document collection.
- Collect, review, and track site regulatory documents for compliance.
- Perform TMF quality control activities and support TMF audits.
- Organize and coordinate internal team and investigator meetings.
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