Jason Parish
- Role
- Senior Clinical Research Associate at IQVIA
- Location
- Raleigh, NC, US
- LinkedIn followers
- 500 followers
Experience
Senior Clinical Research Associate
Oct 2016 — Present
Perform site selection, initiation, monitoring and close out visits in accordance with contracted scope of work and good clinical practices. • Administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Project Manager (CPM), CRS and/or line manager. • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Skills
- Gcp
- Sop
- Ich-Gcp
- Regulatory Submissions
- Edc
- Irb
- Oncology
- Pharmaceutical Industry
- Electronic Data Capture (Edc)
- Protocol
- Clinical Trials
- CRO
- Clinical Monitoring
- Regulatory Affairs
- Ctms
- Clinical Development
- Clinical Research
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