The growing team at the CTU is comprised of a Director of Clinical Trials Operations, Clinical Site Manager, Clinical Trial Associate, and Licensed Clinical Nurses with strong experience in clinical trials. Active private practice with patients available for clinical research or access to patients w...
Key Responsibilities:Provide oversight of clinical development with input on global strategyInterpret and communicate clinical trial dataIdentify new clinical research opportunities and support in-licensing and out-licensing activitiesRequired Qualifications:MD or DO degree from an accredited medica...
Collect, prepare and maintain required research documentation, such as informed consent records, case records, clinical notes and medical reports. Participate in the design, administration and monitoring of clinical trials. ...
Director, Clinical Research Physician in Clinical Development. ...
Report directly to the Clinical Research Manager of the DLD research team and Principal Investigators of relevant studies. We are seeking a Clinical Research Coordinator to join the Division of Digestive & Liver Disease within the Department of Medicine at CUIMC. This role will be instrumental in co...
Key Responsibilities:Lead business development and capture for opportunities within federal agenciesDirect and manage large clinical trials support services contracts or projectsMentor a team of clinical research professionals and foster a culture of continuous improvementRequired Qualifications:Mas...
The Clinical Research Nurse promotes good clinical practices in the conduct of clinical investigations by possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection. The Clinical Research Nurse is responsible for protocol coordi...
The Clinical Research Coordinator provides research coordination support for multiple clinical research projects. The position involves coordinating various clinical research projects, such as registries, retrospective data reviews, long-term follow-up studies, and other non-interventional studies. ...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
The Clinical Research Coordinator (CRC) will provide support for research activities in the Metabolic Bone Diseases Unit. Reporting to the Principal Investigator, the CRC will assist with recruitment, assessment and follow up in research studies. Provide back-up support for clinical trials including...
Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO). Assist multidisciplinary team in research activities. ...
The Clinical Research Nurse promotes good clinical practices in the conduct of clinical investigations by possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection. The Clinical Research Nurse is responsible for protocol coordi...
Unblinded Clinical Research Coordinator I DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. Interpret clinic schedule a...
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructions to site personnel and...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
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 ...
Under the supervision of the investigator(s) and research coordinator, and following established policies and procedures, performs a variety of clinical research activities, and participates in carrying out research objectives, ensuring compliance with all legal, regulatory and protocol guidelines. ...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Supervise staff and perform Clinical Research Coordinator and/or Clinical Research Regulatory Coordinator duties, as applicable. Supervise the organization's clinical research staff including assisting with interviewing, performance improvement, and evaluations. Ensure clinical research policies and...
The Clinical Research Nurse promotes good clinical practices in the conduct of clinical investigations by possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection. Scope of WorkThe Clinical Research Nurse is responsible for pr...
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructio...
The Clinical Research Assistan. As a partner with the Certified Medical Assistants, the position will also work as a MA while not performing clinical research duties. High School diploma; prefer an associate degree for clinical research work. ...