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...
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...
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...
A company is looking for a Senior Director, Clinical Research to lead clinical research programs in nephrology, rheumatology, and infectious diseases. Key Responsibilities:Serve as an independent Medical Monitor for clinical trials from Phase 1 through Phase 3Provide oversight and medical accountabi...
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 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...
Field Clinical Research Specialist. Assist with preparation of/revisions to the Clinical Investigation Plan for assigned clinical studies. Interface with representatives from key functional groups (Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs, Legal, and European Clini...
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...
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. ...
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...
The Clinical Research Coordinator (CRC) will play a vital role in supporting the Division of Nephrology's research activities within the Metabolic Bone Disease Unit. Working closely with the Principal Investigator (PI) and other research staff, you will be instrumental in collecting data and coordin...
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...
Clinical Research Professional or Association of Clinical Research Professionals (ACRP) required for a minimum of 12 months prior to assuming CRC IV role. Provide experienced Clinical Research Coordinator (CRC) support to the Clinical Trials Office (CTO) and Multidisciplinary Team (MDT) team. Bachel...
The Clinical Research Aide will be working with the Principal Investigator, research faculty and staff to support two research programs. The Clinical Research Aide will be responsible for supporting tasks essential for ongoing studies. First research program is a study aiming to understand and impro...
Clinical research certification preferred. Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support andguidance in the clinical trials arena. ...
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. ...
Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO). Assist multidisciplinary team in research activities. ...
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 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...
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. ...
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...
Clinical Research Coordinator I The CRC I will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Liaising with Laboratory team...
POSITION PURPOSE Coordinate and participate in clinical research studies by performing activities involved in the collection, compilation, documentation of research data. The position will work with principal investigators and other research team members to accurately and efficiently carry out a ran...
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...