Sr. Clinical Research Associate Jobs

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861 Sr. Clinical Research Associate jobs found on Monster.

Jobs 1 to 20 of 861
Objectives of the Position To lead and ensure timely implementation of clinical research plans for assigned products or product lines With minimal guidance, coordinate and execute clinical research activities for complex multi-site clinical studies Scope Support the clinical evaluation of RMD products Description of Responsibilities Provide technical input to study designs, clinical developm...
Hologic, Inc. is a leading developer, manufacturer and supplier of premium molecular diagnostic products and services that are used to diagnose human diseases, screen donated human blood and to aid in biomedical research. Hologic is also a leader in the development, manufacturing and sales of medical imaging systems and biopsy devices as well as surgical and treatment products, with an emphasis on...
JOB SUMMARY: Responsible for monitoring and or management of the clinical trial monitoring function of Seattle Genetics clinical trials. This position focuses on coordination of all activities required to initiate, maintain and close -out clinical trials. May lead a clinical trial or selected activities. DETAILED DUTIES & RESPONSIBILITIES TYPICALLY INCLUDE: · May act as Protocol Lead on one or ...
OVERVIEW Focus on the submission of essential documents to the TMF. Responsible for TMF reconciliation. May interact with site staff to follow up on documentation. Participates in the completion of all archiving and final TMF reconciliation and transfers, as required. Skills: 8-10 years experience in clinical research. Strong knowledge of GCPs and regulatory documentation. Education: Bach...
Sr. Clinical Research Associate Location: Princeton, NJ Duration: 6 months Sr. Clinical Research Associate Requirements: -Ideally prefers Oncology nurse (RN); would consider Life Sciences degree with strong clinical oncology background -Lymphoma experience preferred -Clinical oncology background is very important -Must be able to travel up to 30% of the time domestically with the possibilit...
On March 27, 2014, Baxter announced plans to create two independent, publicly traded companies formed around the company's Medical Products and BioScience businesses. The company expects to complete this transaction in mid-2015, subject to market and regulatory approvals. Baxter's Medical Products business will remain a diversified company with a broad global footprint built around fluid systems,...
Senior Clinical Research Associate The Sr. CRA will support the operational management and oversight of aspects of a clinical program. This will involve being part of the management team for a 7000 patient Phase 3 cardiovascular clinical study conducted at over 400 sites internationally. The Sr.CRA will work closely with the Clinical Trial Managers, Medical Monitor, Drug Safety, Clinical Data Man...
SUMMARY: Within the Global Medical Sciences group, independently manages from submission to study close out all activities related to the IST/CTEP Program. Works closely and independently with internal cross-functional IST Review Committee members, external collaboration partners, and external investigators, including key opinion leaders. Independently manages and facilitates the on-line activitie...
PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig...
General Summary: Responsible for implementing set-up, execution, oversight and reporting of clinical studies while ensuring that the conduct of the trial is in compliance with the protocol, ICH/GCP, and applicable regulatory requirements. Key Accountabilities/Core Job Responsibilities: Lead multifunctional team through clinical studies activities that meet ICH/GCP and SOP requirements Develop ...
Kelly Services Plymouth Meeting, PA
Clinical Research Associate (CRA III / Sr. CRA) Our client, a Leading Pharma company is seeking a (CRA III / Sr. CRA) to join their team for a Global Study for a very Long Term Contract. The company has a robust clinical pipeline including an upcoming phase III study. There is tremendous opportunity to work with a collaborative group of scientists and professionals committed to bettering human l...
This role is specifically to assist the 190-201 study team with their data listing reviews. We are looking for a very qualified Sr. CRA (or above) who has had a lot of experience doing data listing reviews. Participates in the planning, oversees, and is accountable for the conduct of clinical studies, with a strong focus on enrollment, quality of data, site relationships, and oversight of challen...
Marten Transport Sunnyvale, CA
In this role, you will design, plan and implement clinical research projects. Your primary responsibilities will involve all operational activities for new and/or ongoing infectious disease and/or cancer diagnostic test product clinical evaluations.This is a 6-month temporary assignment. * Independently responsible for all activities of the clinical trial including clinical site selection, study i...
Where Creating the Best Hope for a Healthier Future Begins... Primary responsibilities include: Provides project management for a wide variety of research experiments, including personnel, facilities, animals, supplies, etc in support of research project desired outcomes, budgets and timelines. Plans methods and procedures for collection of data to provide information needed in medical and healt...
DOCS Global is actively seeking Clinical Research Associates (CRAII), Regional, Lead, and Local Trial Managers in the Boston area who have primary therapeutic experience in Oncology and Cardiology as well as other therapeutic areas. Experience working with multiple protocols is required. Experience facilitating pre-study initiation process, orienting site personnel on protocols and procedures, com...
Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. With a portfolio of leading, science-based offerings in diagnostics, medical devices, nutritionals and branded generic pharmaceuticals, Abbott serves people in more than 150 countries and employs approximately 77,000 people. Abbott is an Equal O...
Marten Transport South San Francisco, CA
Senior Clinical Research Associate The Sr. CRA will support the operational management and oversight of aspects of a clinical program. This will involve being part of the management team for a 7000 patient Phase 3 cardiovascular clinical study conducted at over 400 sites internationally. The Sr.CRA will work closely with the Clinical Trial Managers, Medical Monitor, Drug Safety, Clinical Data Man...
Stryker Communictions Fremont, CA
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 ...
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 ...
Real Staffing Francisco, IN
Job Description: OVERVIEW Focus on the submission of essential documents to the TMF. Responsible for TMF reconciliation. May interact with site staff to follow up on documentation. Participates in the completion of all archiving and final TMF reconciliation and transfers, as required. Skills: 8-10 years experience in clinical research. Strong knowledge of GCPs and regulatory documentation....

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