**** must have 1.5 years of independent monitoring experience****
As a CRA, you will;
Serve as a primary contact point between the sponsor and the investigational site.
Be assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through to data-base lock.
Responsibilities include;
Site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, monitoring and close-out.
Partnering with the CTA, LTM and GTM to ensure overall site management while performing trial related activities for assigned protocols.
May contribute to process improvement and training
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Research
Industries
Pharmaceutical Manufacturing
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