Clinical Research Associate, Medical Devices - Pharma-Cruiting - Life Sciences Executive Recruiters

Position Description

We are seeking a Clinical Research Associate for our Medical Device Client in Newark, California.

Responsibilities:

1) Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40-50% travel) for GCP compliance according to Company SOP
2) Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites
3) Prepare project management reports for clients, project personnel, and management
4) Review and verify CRFs and other clinical data, in-house, for completeness and accuracy; generate queries
5) Resolve queries of CRF data with study site personnel
6) Review Tables and Listings generated from study data
7) Assist in writing Clinical Study Reports

Minimum Requirements:

Two years’ work experience in clinical research, data management, regulatory affairs, or other relevant healthcare research position
Excellent written and verbal communications skills
Ability and willingness to travel in U.S. mainland and Hawaii
Excellent organizational skills and ability to manage time and work independently.


The Ideal Candidate
1+ to 2 years of experience
Minimum Education – High School or Equivalent

Please send your cover letter, resume and salary requirements to tara@pharmacruiting.com

How to Apply

Application Instructions / Send a Resume