Software Guidance & Assistance, Inc., (SGA), is searching for an. Senior Clinical Research Associate. for a. Contract. assignment with one of our premier. Clinical. clients in. Boston, MA. . Position requires heavy travel to site locations in. Minnesota, New Jersey and Illinois. Willing to accept candidates residing anywhere in the US, as long as they can meet the travel expectations and work EST hours to attend daily staff meetings. Responsibili...
Senior CRA. Location: Mid West. We require Sr. CRAs (10 years of experience across multiple indications) to travel to sites to complete site monitoring activities in compliance with the monitoring plan. Below are the requirements. Sr. CRA with at least 10 Years Experience. Sponsor Experience. Cell/Gene Therapy and Rare Disease Experience. Early and Late Phase Studies. Start Up, Maintenance, and Close Out Experience. Below are the general responsi...
Overview. (Senior) Clinical Research Associate. Location: Sydney (hybrid). . As a (Senior) Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. . You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where peo...
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today. Everest has been an independent CRO since 2004 with a strong foundatio...
Job description. Position Summary. . The Sr. Clinical Research Associate will oversee outsourced clinical operations activities including but not limited to site management, site monitoring and site level TMF filing. Additional responsibilities may be assigned (e.g. management of central labs). Job Duties. . Oversee outsourced clinical trial monitoring by reviewing monitoring plans, monitoring visit reports, deviation listings, and conducting per...
Job Description. Job Description. Cartesian Therapeutics is reimagining cell therapies with transformative technologies to bring a new generation of treatment options to patients with autoimmune diseases. With recent company growth, we are seeking a highly skilled and experienced Clinical Research Associate (CRA) with a strong background in Phase I-III clinical trials, particularly in the. Autoimmune. therapeutic area, with desired expertise in. ...
This is what you will do. The Senior Clinical Research Associate (Sr. CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local country team(s). The Sr.CRA works in close collaboration with other CRAs and the Country Operations Management (COM) Team to ensure that study commitments are achieved in a timely and efficient manner. The Sr.CRA acts as the main contact with the study site...
Job Description. Senior CRA. Responsibilities include. All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties. All aspects of site and registry management as prescribed in the project plans. Organize and make presentations at Investigator Meetings. Report, write...
Job Description. Senior CRA. Responsibilities include. All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties. All aspects of site and registry management as prescribed in the project plans. Organize and make presentations at Investigator Meetings. Report, write...
Job Description. Senior CRA. Responsibilities include. All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties. All aspects of site and registry management as prescribed in the project plans. Organize and make presentations at Investigator Meetings. Report, write...
Job Description. Senior CRA. Responsibilities include. All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties. All aspects of site and registry management as prescribed in the project plans. Organize and make presentations at Investigator Meetings. Report, write...
