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Sr. Clinical Research Associate Jobs

32 jobs

TalentMine is actively hiring Sr. CRA's for a leading company within the Pharmaceutical industry. This is an exciting opportunity to take your skills as a CRA to the next level. If you are looking for upward mobility at a great company, please send resumes to ***** for more information. Responsibilities: Monitors and manages clinical trials Site Visits: Qualification, I...
Sr. Clinical Research Associate (CRA) needed to perform/coordinate all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and company Standard Operating Procedures. • Conducts site visits to assess protocol and regulatory compliance and manages required documentation • Responsible for ensuring that data...
Sr. Clinical Research Associate (CRA) needed to perform/coordinate all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and company Standard Operating Procedures. • Conducts site visits to assess protocol and regulatory compliance and manages required documentation • Responsible for ensuring that data...
Monitors and/or supervises the monitoring activities of assigned clinical trials to ensure data integrity and adherence to Federal regulations, company policies, and any other applicable procedures. Acts as project resource to study, site, and in-house personnel regarding the product under test and the clinical trial conduct. Responsible for supporting Comply with applicable Regulations, ICH/GCP ...
JOB SUMMARY: This position focuses on coordination of all clinical operations site management and monitoring activities required to initiate, monitor and complete clinical programs at the clinical trial site level. May act as mentor for less senior members of the Clinical Trial Team. Provide the clinical operation input to the clinical project team. DETAILED DUTIES & RESPONSIBILITIES TYPICALLY I...
About Avanir Pharmaceuticals, Inc. ( www.avanir.com ) Avanir Pharmaceuticals, Inc. is a biopharmaceutical company focused on bringing innovative medicines to patients with central nervous system disorders of high unmet medical need. As part of our commitment, we have extensively invested in our pipeline and are dedicated to advancing medicines that can substantially improve the lives of patients ...
Sr. Clinical Research Associate • 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,...
About Avanir Pharmaceuticals, Inc. ( www.avanir.com) Avanir Pharmaceuticals, Inc. is a biopharmaceutical company focused on bringing innovative medicines to patients with central nervous system disorders of high unmet medical need. As part of our commitment, we have extensively invested in our pipeline and are dedicated to advancing medicines that can substantially improve the lives of patients a...
Requisition ID 9427BR Job Title Sr. Clinical Research Associate Group MedSurg and Neurotech Division Neurovascular Business Function Clinical Affairs Country United States State/Province CA City Fremont Employment Category Full Time Percent Travel Required Up to 40% Shift 1st About Stryker Stryker is one of the world’s leading medical technology companies and together with our customers...
Overview: The Sr. Clinical Research Associate is responsible for conducting the day-to-day management of activities associated with the execution of clinical trials. The Sr. CRA ensures that clinical tasks are being performed in compliance with all regulations, Good Clinical Practices, and company policies and procedures. The Sr. CRA will be responsible for data management, study materials and lo...
Southborough, MA - The Senior Clinical Research Associate is a member of the Clinical Affairs team responsible for performing activities essential to providing clinical guidance, strategy and support for the development of new technologies and products. The incumbent will assist in the design, development, organization, implementation and evaluation of scientifically valid clinical research. He/Sh...
The Senior CRA role is integral to driving project success. This position will independently manage and monitor clinical trial sites, and will function as the Lead CRA on select projects. In the Lead role, this position will be responsible for providing direction to and training for other CRAs assigned to those projects. The Sr. CRA/Lead CRA will be responsible for ensuring that sites and CRAs op...
This Senior Clinical Research Associate (Senior CRA) position represents Rho in the global medical research community while developing and maintaining collaborative relationships with investigational sites and client company personnel. The Senior CRA performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guid...
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team, our Clinical Research Associates (CRA’s) identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV ensuri...
Sr. Clinical Research Associate• 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 Site Managers and/or Protocol Managers, where applicable, to orient and train site personnel regarding the protocol and applicable regulatory requirements.• Identifies, evaluates, and ...
Sr. Clinical Research Associate• 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 Site Managers and/or Protocol Managers, where applicable, to orient and train site personnel regarding the protocol and applicable regulatory requirements.• Identifies, evaluates, and ...
JOB SUMMARY: This position focuses on coordination of all clinical operations site management and monitoring activities required to initiate, monitor and complete clinical programs at the clinical trial site level. May act as mentor for less senior members of the Clinical Trial Team. Provide the clinical operation input to the clinical project team. DETAILED DUTIES & RESPONSIBILITIES TYPICALLY I...
Requisition ID 9427BR Job Title Sr. Clinical Research Associate Group MedSurg and Neurotech Division Neurovascular Business Function Clinical Affairs Country United States State/Province CA City Fremont Employment Category Full Time Percent Travel Required Up to 40% Shift 1st About Stryker Stryker is one of the world’s leading medical technology companies and together with our customers...
Monitors and/or supervises the monitoring activities of assigned clinical trials to ensure data integrity and adherence to Federal regulations, company policies, and any other applicable procedures. Acts as project resource to study, site, and in-house personnel regarding the product under test and the clinical trial conduct. Responsible for supporting Comply with applicable Regulations, ICH/GCP ...
Perform all phases of clinical site management from site identification and qualification through site closure to ensure the integrity of clinical data with respect to accuracy, accountability and documentation through review of case report forms, source documents, and medical records. Ensure documentation at study sites are maintained according to FDA regulations and ICH-GCP guidelines, and coll...