The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Clinical Research Coordinator I - Obstetrics & Gynecol...
We are a global Clinical Research Institute that has been conducting Clinical Trials over the last 25 years. Clinical Research Coordinator (sponsor-backed trials) Highly Preferred BA/BS in a scientific discipline. We have successfully completed over 1,000 clinical studies together with our primary. ...
The Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each...
The Clinical Research Coordinator will be responsible for supporting the planning, implementation, and coordination of clinical trials conducted within our site network. Minimum of [insert number] years of experience in clinical research coordination or related role, preferably in a clinical trial s...
Onsite in San Diego, 92108 area.Strong CRC must have strong attention to detail and will be focusing on a lot of data entry/administrative tasks....
The Clinical Research Coordinator II is crucial to the companies clinical research, managing multiple complex trials across various areas and phases. An exciting Clinical Site Network are looking to bring on board a Clinical Research Coordinator to either of their sites based out of. Minimum of 3+ y...
Onsite in San Diego, 92108 area.Strong CRC must have strong attention to detail and will be focusing on a lot of data entry/administrative tasks....
Under the direction of Research Institute Management, the Clinical Research Nurse Coordinator II is responsible for providing coordinator assistance for sponsored clinical studies within the Center for Clinical Research in accordance with Institutional policy, Good Clinical Practice and ICH guidelin...
The position of Cardiovascular Clinical Research Coordinator supports, facilitates, and coordinates daily clinical trial activities for assigned studies and plays a critical role in the conduct of the study, including study start-up, recruitment and enrollment, subject management, data management, a...
Remain in communication with clinical research project coordinators, Principal Investigators, and other research staff. TES has current openings for Clinical Research Coordinator Assistants. The incumbents will be responsible for assisting with data entry and database corrections for various researc...
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Clinical Research...
Under supervision from Principal Investigator and Clinical Research Supervisor II in the Pulmonary, Critical Care & Sleep Medicine Division, the Research Coordinator supports the ICU clinical research efforts for a variety of research projects and clinical trials focusing primarily on pulmonary diso...
Association of Clinical Research Professionals Certified Professional (ACRP-CP), Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC). Preferred: Clinical research experience in a hospital setting and/or pediatric clinical research experience. Required: M...
Demonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital. The Clinical Research Coordinator will plan, develop and implement start-up procedures for multiple phase I-III research studies in a...
Odyssey Systems Consulting Group, .We focus on people, processes, and performance to deliver superior results.Since our inception in 1997, our commitment to mission success and customer satisfaction has been recognized with exponential growth and exceptional past performance ratings.We accept challe...
The incumbent will work as an Assistant Clinical Research Coordinator to be responsible for coordinating and managing a clinical trial conducted by the Pacific Treatment and Research Center (Pac-TARC) at UC San Diego. Experience performing clinical research duties in a clinical research environment....
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...
The Research Coordinator will assist an Investigator, Research Associate, or Project Manager in operationalizing tasks associated with implementing a research study. Minimum 3 years in Clinical Research and preference for relevant healthcare experience. Key duties include recruiting and consenting r...
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...
Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or equivalent Clinical research certification through SOCRA for ACRP. Under supervision, the Clinical Research Coordinator will be assigned to assist with multiple clinical research studies involving hum...
Under supervision from Principal Investigator and Clinical Research Supervisor II in the Pulmonary, Critical Care & Sleep Medicine Division, the Research Coordinator supports the ICU clinical research efforts for a variety of research projects and clinical trials focusing primarily on pulmonary diso...
The Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each...