Clinical Research Associate - IL IN WI MN
A company is looking for a Clinical Research Associate in the United States.Key Responsibilities : Conducting clinical monitoring activitiesCollaborating with healthcare professionalsEnsuring compliance with protocols and regulationsRequired Qualifications : Bachelor's degree in a related fieldExperience in clinical research or healthcare industryFamiliarity with regulatory requirementsAbility to travel as needed
Cancer Clinical Research Coordinator Associate - BMT
Reporting to the BMT-CT Clinical Trials Operations Manager (CTOM), the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to to manage data, enroll and follow patients on trial, and assist with regulatory and f...
Neuromuscular Clinical Research Coordinator Associate
The position will include working with neuromuscular patients in clinic, educating them on Stanford neuromuscular research studies, consenting participants, and coordinating sample collections during clinic visits. The position will coordinate the oversight and implementation of research protocols a...
Clinical Research Coordinator Associate (50% FTE)
Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and re...
Clinical Research Coordinator Associate (50% FTE)
Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and re...
Clinical Research Coordinator Associate
The CRCA will coordinate all aspects of the study including but not limited to participant communication, conducting in-person assessments, collecting and entering data, and ensuring protocol compliance. Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate d...
Clinical Research Associate
Maintain project files and Trial Master File (TMF) documentation, including ethics committee approvals, investigator CVs, protocols, and other essential study documents. Conduct site evaluation visits, site initiation visits, interim monitoring visits, and close-out visits in accordance with study p...
Sr Clinical Research Associate (CRA)/Principal CRA - West
Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. With clinical trials conducted...
Clinical Research Associate (CRA II/Senior) - West (Oncology)
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines while also Ensuring compliance with the approved standard operating proc...
Senior Clinical Research Associate/Clinical Research Associate II
The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well-being of human subjects are protected, evaluating the quality and integrity of the reported data, evaluating the site efficacy of staff training and requiring retraining where nece...
Clinical Research Associate (CRA II/Senior) - West
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines while also Ensuring compliance with the approved standard operating proc...