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
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation for trial inclusion. Suppo...
Histologist Clinical Research Associate
A company is looking for a Histologist - CRA I to support diagnostic studies. ...
Academic Scholar – Clinical or Research Assistant, Associate or Full Professor, Department of Pediatrics, Division of Neonatology
UBMD Pediatrics is one of 18 practice plans within UBMD Physicians’ Group, the single largest medical group in the area, and we are supported by 14 pediatric subspecialties. Candidates must show evidence of continued excellence in clinical practice, such as innovative accomplishments in delivery of ...
Senior Clinical Research Associate
A company is looking for a Senior Clinical Research Associate responsible for monitoring clinical trials and ensuring compliance with regulatory standards. ...
Clinical Research Associate I
Takes a leadership role in the clinical research mission of the organization and Clinical Research Services (CRS) through the management of projects within the research regulatory requirements and careful adherence to the Code of Federal Regulations (Title 21) and guidelines set up by the Internatio...
Oncology Clinical Research Associate - IQVIA Biotech at IQVIA
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 I
Supports the clinical research mission of the organization and Clinical Research Services (CRS) through one of the following areas: (1) the maintenance of research regulatory documents and the submission of new studies, amendments, continuing reviews and all other study documents; (2) data collectio...
Environmental Project Manager - Industrial Hygiene (IH)
Manage project budgets and prepare monthly invoices. Training junior staff and managing projects with one or more field technicians on-site. ...
Research Assistant (Remote)
D Aceto Services LLC is seeking a motivated and detail-oriented Research Assistant to join our remote team. In this role, you will support various research initiatives by collecting, analyzing, and interpreting data to provide insights that drive decision-making. This position is ideal for individua...