A company is looking for a Study Start-Up Clinical Research Associate (SSU CRA) to manage site selection and activation phases of clinical trials.
Key ResponsibilitiesCollaborate with teams to identify and activate clinical trial sitesPrepare and manage regulatory submissions and start-up documentationTrack and manage essential documents to ensure timely site activationRequired QualificationsBachelor's degree in life sciences, nursing, or a related fieldAt least 2 years of experience in Site Selection Visits and Study Start-Up activitiesExperience with Informed Consent Forms (ICF) review is desiredKnowledge of ICH-GCP guidelines and local regulatory requirementsStrong organizational skills with a focus on timelines and deliverables
Study Start-Up Clinical Research Associate
A company is looking for a Study Start-Up Clinical Research Associate (SSU CRA) to manage site selection and activation phases of clinical trials. ...
Clinical Research Associate (CRA) - Dallas
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Hybrid work-from-home options (dependent upon position and level). Competitive PTO packages, starting at 20...
Senior Study Start-Up Specialist
A company is looking for a Contract Senior Study Start-Up Specialist responsible for overseeing and leading study start-up activities in collaboration with clinical research stakeholders. ...
Clinical Research Associate (CRA) - BS or Advanced Degrees in Life Sciences
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Hybrid work-from-home options (dependent upon position and level). Competitive PTO packages, starting at 20...
Clinical Research Associate
A company is looking for a Clinical Research Associate to support multiple projects in the healthcare field. ...
Clinical Research Associate, Sponsor Dedicated
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Create and maintain appropriate documentation regarding site management, monitor...
Clinical Research Associate - Oncology - Texas / Louisiana
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. Develops site ...
Clinical Research Associate AIM Center
The Clinical Research Associate for the AIM center works directly with the AIM Center Imaging Scientist and other investigators for research projects; as well as other clinical disciplines utilizing AIM Center imaging services. Job Title & Specialty Area: Clinical Research Associate AIM Center. Prim...
Research Associate, Forum (Immediate Start)
Research and identify the most relevant individuals (C-level executives and practitioners working at the heart of their industries) to take part in conference calls, private meetings and roundtables on key investment catalysts . Demonstrable skill in carrying out research with a logical and focused ...
Clinical Research Associate - Southeast - Early Development
We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II for early phase trials. ICON plc is a world-leading healthcare intelligence and clinical rese...