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Regional CRA Jobs

338 jobs

Pharm-Olam International has one of the largest global footprints of any CRO. We are currently seeking experienced candidates to fill the roles of: **CRA II/CRA III/SCRA's** West Coast/Midwest/Central US (regional positions) 50-75% travel, which will vary based on the phase of assigned study/ies. These are full-time, home-based positions. Required Attributes: Minimum of 3 plus years’ monitor...

DOCS! We are hiring CRA/SCRA for one of the top Global CRO and world's leading pharmaceutical company across many different therapeutic areas in United States. Kindly do share your updated resume to proceed further and one of our regional recruiter will get touch base with you directly for your further queries. Job Requirements - Four year degree required (B.A, B.Sc) - Minimum 3+ years recent ...

Worldwide Clinical Trials is a therapeutically focused global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract research organizations, we offer exceptionally strong clinical trial methodology integrated with an effective global operations network. We are currently seeking hi...

Worldwide Clinical Trials is a therapeutically focused global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract research organizations, we offer exceptionally strong clinical trial methodology integrated with an effective global operations network. We are currently seeking hi...

Worldwide Clinical Trials is a therapeutically focused global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract research organizations, we offer exceptionally strong clinical trial methodology integrated with an effective global operations network. We are currently seeking hi...

Hays Life Sciences is currently partnered with a growing CRO to assist in their search for Home- based Regional CRAs throughout the continental United States and Canada. This CRO deals with Clinical Trials from the early development stage to post-approval. In this capacity, you will play a large role in clinical trials. In this position you will conduct site visits to assess protocol and regulato...

Looking for Regional CRA's * any location *Perm * open therapy * minimum 5years of experence; Overview of the Role: - Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for...

DOCS is actively seeking a Regional CRA with Oncology experience. May require up to 50% travel. Responsibilities include: -Coordinate monitor, reviews and generate queries of CRF's for clinical trials -Interface with, and assure training of investigators, center staff, trial monitors and clinical staff -Ensure adequate monitoring is conducted on all clinical trials including identification of...

DOCS is actively seeking a Regional CRA with Oncology experience. May require up to 50% travel. Responsibilities include: -Coordinate monitor, reviews and generate queries of CRF's for clinical trials -Interface with, and assure training of investigators, center staff, trial monitors and clinical staff -Ensure adequate monitoring is conducted on all clinical trials including identification of...

DOCS is actively seeking aRegional CRA with Oncology experience.May require up to 50% travel.Responsibilities include:-Coordinate monitor, reviews and generate queries of CRF's for clinical trials-Interface with, and assure training of investigators, center staff, trial monitors and clinical staff-Ensure adequate monitoring is conducted on all clinical trials including identification of issues and...

CRA role: •Expedites the pre-study and study initiation processes including the conduct of Pre-Study valuation and Site Initiation visits. •Conducts Site Initiation visits in collaboration with RCO Site Managers and/or GCO&S Protocol Managers, where applicable, to orient and train site personnel regarding the protocol and applicable regulatory requirements. •Identifies, evaluates, and recommend...

Serves as primary contact point between the sponsor and investigational sites.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 data-base lock. Responsibilities include site selection, pre-trial...

Serves as primary contact point between the CRO. sponsor and investigational sites. A Site Manager 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 start-up through data-base lock. Responsibilities include s...

CRA role: •Expedites the pre-study and study initiation processes including the conduct of Pre-Study valuation and Site Initiation visits. •Conducts Site Initiation visits in collaboration with RCO Site Managers and/or GCO&S Protocol Managers, where applicable, to orient and train site personnel regarding the protocol and applicable regulatory requirements. •Identifies, evaluates, and recommend...

Serves as primary contact point between the CRO, sponsor and investigational sites.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 data-base lock. Responsibilities include site selection, pre-...

DOCS is actively seeking aRegional CRA with Oncology experience.May require up to 50% travel.Responsibilities include:-Coordinate monitor, reviews and generate queries of CRF's for clinical trials-Interface with, and assure training of investigators, center staff, trial monitors and clinical staff-Ensure adequate monitoring is conducted on all clinical trials including identification of issues and...

Requisition ID 32435BR Title Regional Clinical Research Associate (CRA)-Biopharm-LA/Orange County Job Category Clinical Trial Management Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regul...

Requisition ID 32436BR Title Regional Clinical Research Associate (CRA) - Cleveland, OH Job Category Clinical Trial Management Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and...

Requisition ID 32438BR Title Regional Clinical Research Associate (CRA) - Sacramento, CA Job Category Clinical Trial Management Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations an...

Requisition ID 32439BR Title Regional Clinical Research Associate (CRA) - Pittsburgh, PA Job Category Clinical Trial Management Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations an...