Sr. Clinical Research Associate Jobs

582 jobs

May independently design, plan and implement, and provide overall direction of clinical research projects. Managing all aspects of unblinded assigned clinical studies to ensure studies are completed on time, within budget, and in compliance with Good Clinical Practice (GCP), government regulations, and overall clinical objectives. Develop protocols, investigator brochures and study reports, and as...

Daily activities will vary depending on the clinical phase of the program. Will have responsibilities for managing more than one project. Determine methods and procedures for performing new assignments. The Senior Clinical Research Associate may oversee the activities of CTAs and CRAs. Manage contract research organization (CRO) personnel and study sites to ensure studies are completed on time, w...

Sr. Clinical Research Associate (Senior 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 but Permanent preferred. The company has a robust clinical pipeline including an upcoming study. There is tremendous opportunity to work with a collaborative group of scientists and professionals committed to better...

Are you looking for a new opportunity, with a leading medical device company? Look no further! My client is a renowned Medical Device Company, and they are looking for a Sr. Clinical Research Associate! This is a contract to hire position. Among others, the Clinical Research Associate will have the following responsibilities: Clinical study site management, including: site and study initiation, ...

Perform site management including tracking of essential clinical trial documentation, training of site staff on study procedures, and monitoring of site adherence to protocol specified procedures. Must use detailed knowledge of assigned protocols and Manual of Operations to ensure quality and deliverables are met across sites; Conduct initial review of adverse event reports for completeness prio...

Clinical Research Associate / Medical Device We are seeking Sr. CRAs for Career Monitoring Positions for one of the largest medical device companies in the U.S. You DO NOT need device monitoring experience to qualify. These coveted opportunities are few and far between and will be filled very fast. We offer excellent compensation, benefits and long-term stability. We are looking for monitors in...

Clinical Research Associate / Medical Device We are seeking Sr. CRAs for Career Monitoring Positions for one of the largest medical device companies in the U.S. You DO NOT need device monitoring experience to qualify. These coveted opportunities are few and far between and will be filled very fast. We offer excellent compensation, benefits and long-term stability. We are looking for monitors in...

Clinical Research Associate / Medical Device We are seeking Sr. CRAs for Career Monitoring Positions for one of the largest medical device companies in the U.S. You DO NOT need device monitoring experience to qualify. These coveted opportunities are few and far between and will be filled very fast. We offer excellent compensation, benefits and long-term stability. We are looking for monitors in...

This is a home-based position in AL, AR, CI, DE, DC, FL, GA, KY, LA, ME, MD, MA, MS, NH, NJ, NY, NC, OH, PA, RI, SC, TN, VT, VA and WV. PPD - Local Community. Global Reach. Our global team of experienced CRA Managers work to ensure that our CRAs have an appropriate work load, the tools they need to be successful and that there is a plan for their continued career advancement. PPD CRAs also enjo...

TechData is looking for Outcome Research Biostatistician, Biostatistician/SAS Programmer/Statistical Programmer (Some can be telecommuting), Medical Writer, Clinical Database Programmer, Sr. Study Manager, Clinical Research Scientist/Associate, Drug Safety Associate, Clinical Data Manager inNorthern and Central NJ.Please see below requirements and send your resume to: *****...

Our Client on the Peninsula is looking for a Sr. Research Associate to join their team! Sr. Research Associate Duties: As part of the Product Development/Analytical group the Sr. Research Associate will support: preformulation, formulation, analytical method development and product characterization using a variety of analytical methods with a focus on HPLC and aerosol analysis proprietary dry p...

Associate Clinical Trial Manager/Clinical Trial Manager/Senior Clinical Trial Manager (NJ, MA, CT) Overview: The Associate Clinical Trial Manager (Branford, CT) / Clinical Trial Manager (NJ, MA, CT) / Senior Clinical Trial Manager (NJ, MA, CT) works closely with internal team members and vendors to ensure that assigned clinical trials are conducted per protocol, in a timely fashion and in a mann...

Associate Clinical Trial Manager/Clinical Trial Manager/Senior Clinical Trial Manager (NJ, MA, CT) Overview: The Associate Clinical Trial Manager (Branford, CT) / Clinical Trial Manager (NJ, MA, CT) / Senior Clinical Trial Manager (NJ, MA, CT) works closely with internal team members and vendors to ensure that assigned clinical trials are conducted per protocol, in a timely fashion and in a mann...

Associate Clinical Trial Manager/Clinical Trial Manager/Senior Clinical Trial Manager (NJ, MA, CT) Overview: The Associate Clinical Trial Manager (Branford, CT) / Clinical Trial Manager (NJ, MA, CT) / Senior Clinical Trial Manager (NJ, MA, CT) works closely with internal team members and vendors to ensure that assigned clinical trials are conducted per protocol, in a timely fashion and in a mann...

Serves as primary contact point between the sponsor and the investigational site. 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 sit...

PURPOSE: Responsible for the support of assigned sites in accordance with Good Clinical Practice (GCP), ICH guidelines, federal regulations and SOPs. Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within CMR. May be responsible for monitoring assigned sites in accordance with GCP/ICH and NNI SOPs. RELATIONSHIPS: Reports to a Man...

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 69,000 people. Abbott is an Equal O...

Clinical Research Associate (Senior CRA and CRA II) Theorem Clinical Research is currently hiring talented, dedicated CRA's. These are remote, home-based opportunities open to most US locations. Immediate opportunities available in the following areas: respiratory, neurology, women’s health, oncology, musculoskeletal, medical device, cardiovascular and Phase I. In this role, the CRA is responsi...

At Boston Children’s Hospital, success is measured in patients treated, parents comforted and teams taught. It’s in discoveries made, processes perfected, and technology advanced. In major medical breakthroughs and small acts of kindness. And in colleagues who have your back and patients who have your heart. As a teaching hospital of Harvard Medical School, our reach is global and our impact is pr...

Responsibilities Job Functions: • Responsible for both project management and trial execution by conducting all activities related to the set up, initiation, conduct and completion of clinical trials. • Perform routine site visits, including Pre-Study, Initiation, Routine, and Closeout visits. Visits to include monitoring of proper informed consent procedures, source document verification, and ...