National Institute of Clinical Research, a research organization serving the pharmaceutical and biotech industries, is searching for a Clinical Research Coordinator with 2 or more years of experience.
Duties for this position will include managing the study from placement to completion of the final study report. The CRC is responsible for the conduct of quality and efficient clinical trials.
REQUIREMENTS : A minimum of 2 years of clinical research experience is preferred. In-depth knowledge of the clinical research process, including Good Clinical Practices and ICH guidelines;
Strong interpersonal and communication skills; excellent attention to detail; exceptional organizational and planning skills.
Able to project and coordinate study needs in advance. Candidate needs to have good troubleshooting and conflict-resolution skills.
Being bilingual in English / Spanish is a plus!
NICR is an independent, multi-site clinical trial management organization (SMO). We deliver and facilitate, the highest quality clinical trial management to our multi-specialty network of affiliated physicians and researchers across California and Texas.
Candidates must be local to the Victorville & Barstow area.
Location(s)
Victorville & Barstow, CA
Employment Type
- Full-time
- This is not a remote position
Benefits :
- Medical Insurance, Dental Insurance, Vision Insurance, 401k, PTO
Clinical Research Coordinator
Roles on our site support the coordination and management of clinical research activities and involve working closely with research teams to oversee daily study operations and ensure compliance with all regulatory requirements. Provide guidance and training to clinical research staff. Assist with ma...
Clinical Research Coordinator- 233018
The Clinical Research Coordinator must also be able to perform clinical. Maintain and update research fund accounting files, research billing, budgets and. Writes patient information sheet for clinical studies for submission to IRB, as well as. Writes patient information sheet (ICF) for clinical stu...
Clinical Research Coordinator
Assist the field Clinical Development team with administrative tasks for all clinical trials, including tracking study status and enrollment, managing research budgets, and maintaining up-to-date regulatory documents as required. Coordinate and organize clinical staff resources for internal research...
Clinical Research Nurse Coordinator II, Oncology
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...
Clinical Research Coordinator I - Kerlan Jobe Institute
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 ...
Clinical Research Coordinator II (Oncology)
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...
Clinical Research Coordinator II - Pediatric Neonatology - Full-Time, Hybrid
The Clinical Research Coordinator II 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 e...
Clinical Research Coordinator
National Institute of Clinical Research, a research organization serving the pharmaceutical and biotech industries, is searching for a Clinical Research Coordinator with 2 or more years of experience. In-depth knowledge of the clinical research process, including Good Clinical Practices and ICH guid...
Clinical Research Coordinator I - Obstetrics & Gynecology - Maternal-Fetal Medicine (Part-Time, Hybrid)
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 ...
Project Coordinator
The project coordinators main role is to assist the Senior Project Lead of GoodShop with:. Interfacing with clients, vendors and design team to ensure all project deadlines are met. Organization of past and current projects. Project Management experience preferred. ...