Ref #: 27874

Employment type: Permanent - Full-Time

Location: Mid-Atlantic USA

Posted: 22-Mar-2021

Description

Clinical Research Associate: Mid-Atlantic USA – Remote

• The Clinical Research Associate is 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 study planning through data-base lock.
• Responsibilities include study planning, study start-up and study closeout.
• Delivers results that have direct impact on the successful completion of the study.
• Collaborate with the CTA and CSM to ensure overall site management while performing study related activities for assigned protocols.
• Collaborate with the CTA and CSM to ensure overall site management while performing study related activities for assigned protocols.

Qualifications:
Bachelor’s degree in B.Sc. or other degree in Life Sciences or equivalent. Must have experience in Clinical Research or equivalent qualification. A Minimum 1 – 2 years of monitoring experience.

DOCS is the FSP division of ICON Clinical Research. We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.

DOCS is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.

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