Intern, Clinical Trial Operations
About The Position
This is a unique opportunity as a junior Clinical Trial Assistant in Clinical Operations, initially reporting to the Associate Director/Director Clinical Operations, you will be responsible for acting as a central contact for the clinical study teams and assist with the clinical execution and management to support RevMed clinical trials. Assisting in the review, distributing, and archiving of study specific documents and reports (plans, training materials, study guides, manuals etc.). Assisting with updating and maintaining clinical systems and any reporting tools. Support maintenance of the trial master files (TMF) if applicable, or work with CRO to audit and resolve discrepancies. Create, maintain, and track information for key study related activities. Assisting in the preparation of meeting materials, scheduling meetings, for internal clinical operation team meetings. Working with cross functional study teams, and vendors to assist in the coordination of clinical trial activities. Support other clinical operations activities as appropriate.
Requirements
- Currently enrolled at an accredited college/university as a rising senior or higher in a Bachelor’s degree in biological sciences or related health related field.
- Demonstrate proficiency in Microsoft Word, Excel and PowerPoint and other software platforms.
Nice To Haves
- Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.
- Excellent written and verbal communication and interpersonal skills.
- Demonstrated ability to multi-task, prioritize options.
Responsibilities
- Acting as a central contact for the clinical study teams
- Assist with the clinical execution and management to support RevMed clinical trials
- Assisting in the review, distributing, and archiving of study specific documents and reports (plans, training materials, study guides, manuals etc.)
- Assisting with updating and maintaining clinical systems and any reporting tools
- Support maintenance of the trial master files (TMF) if applicable, or work with CRO to audit and resolve discrepancies
- Create, maintain, and track information for key study related activities
- Assisting in the preparation of meeting materials, scheduling meetings, for internal clinical operation team meetings
- Working with cross functional study teams, and vendors to assist in the coordination of clinical trial activities
- Support other clinical operations activities as appropriate
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What This Job Offers
Career Level
Intern
