Participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelors degree with 4+ year experience as a Clinical Trials Asso...
Key Responsibilities:Develop government customer-oriented and regulatory, clinical research-grade data products and insights platformsEnsure data products meet the needs of customers seeking regulatory submissions and real-world data clinical research questionsOwn the execution of data product-relat...
The CTRC supports innovative, patient-oriented research, offers clinical research training and recognition programs, and provides researchers with an environment for seeing patients when they take part in clinical research studies. To learn more, please visit Clinical & Translational Research Center...
A company is looking for a Contract Clinical Research Associate with IVD Experience. ...
Reporting to the Lead Clinical Research Associate, the CRA II/Sr. This role will collaborate closely with key cross-functional internal stakeholders including Clinical Operations, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendo...
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. ...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
Excellentknowledge of Clinical Research methods andprocedures. Scor other diploma from a Clinical Researchprogram. Avalid Clinical Researchlicense. Yourexpertise and opinions shall be valuable to us which shall help usin ourresearch. ...
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 ...
M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). As a Clinical Research Physician, you will provide ...
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...
A global role reporting into Senior Manager, Clinical Research Pharmacy Services supporting IP Management specific deliverables in Clinical Trial Execution. Broad work experience in life sciences or medically related field, including biopharmaceutical clinical research experience working on clinical...
The UCLA Center for LGBTQ+ Advocacy, Research, and Health (C-LARAH) is part of the Fielding School of Public Health, within the Department of Epidemiology. The mission of C-LARAH is to maintain an interdisciplinary, research-driven, evidence-based platform used to carry out public policy initiatives...
We are seeking a Clinical Research Associate I (CRAI) who will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. This role is responsible for completing case report forms (CRFs) and ...
Be part of one of the largest and fastest-growing clinical research companies in the United States with potential internal growth and advancement. Work alongside a successful and dynamic team conducting clinical trials for new medications and treatment in various therapeutic areas not limited to gen...
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...
As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ...
The Clinical Research Coordinator will be the main operational interface with study subjects during the conduct of a clinical trial. Resolves study source document discrepancies including supervising and reviewing completion of documentation of discrepancies by clinical research staff. Schedules and...
Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Minimum one (1) year of training and/or experience in research methodol...
Clinical research related experience with two years assisting, supporting and/or participating in coordination of clinical research trials required. The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibilit...
The Clinical Research Coordinator Supervisor (CRC-Su) functions independently and is responsible for the complete coordination of multiple assigned human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Cl...
The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other CRA team members within established protocols and portfolio under general supervision. Works with Clinical Trial Oversight Managers (CTOM...
The CRC II may assist with the training and/or mentoring of CRC I or other CRC II staff on the basics of clinical research, Good Clinical Practice (GCP), Good Documentation Practices (GDP), Standard Operating Procedures (SOPs) and other related aspects of the clinical study. Responsible for the over...
Under moderate supervision, the Clinical Research Coordinator I (CRC-I) is expected to perform all core Clinical Research Coordinator (CRC) responsibilities for human subjects’ (clinical) research. Preferred: Clinical research experience in a hospital setting and/or pediatric clinical research exper...
The Senior Clinical Research Coordinator (CRC) works collaboratively with Principal Investigators (PI) sub-investigators, clinical and ancillary departments, to lead research studies in subject recruitment, data collection, scheduling of study start-up, study related activities and follow-up of enro...