Intern Cta

**Essential Functions**
Assist Clinical Research Associates (CRAs)/In-house Clinical Research
Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately
updating and maintaining clinical systems that track site compliance and
performance within project timelines.
Assist the clinical team in the preparation, handling, distribution, filing, and
archiving of clinical documentation and reports according to the scope of
work and standard operating procedures. Assist with periodic review of study
files for completeness.
Assist CRAs/iCRAs and RSU with preparation, handling and distribution of
Clinical Trial Supplies and maintenance of tracking information. Assist with
the tracking and management of Case Report Forms (CRFs), queries and
clinical data flow. Act as a central contact for the clinical team for designated
project communications, correspondence and associated documentation.
May accompany CRAs on site visits to assist with clinical monitoring duties
upon completion of required training and with required approval. May perform
assigned administrative tasks to support team members with clinical trial
execution.

**Qualifications**
- Bachelor's Degree Pursuing degree Req
- Appropriate verbal and written communication skills to function within a professional work environment.
- Evidence of effective problem - solving, analytical, and critical thinking skills.
- Proficiency in alignment with the desired role placement
- Evidence of strong team work and communication skills.