Director, Clinical Research Physician in Clinical Development. ...
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum of 3 years’ experience in monitoring pharmaceutical industry clinical trials. Have an in-depth knowledge of Good Clinical Practice, ICH g...
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...
Responsibilities include but are not limited to: coordinating the data management activities of the CPDM, while providing supervision and delegation of work assignments and evaluation of the CPDM Clinical Research Coordinators (CRCs) and Data Coordinators(DCs); creating and promoting professional de...
A company is looking for a Clinical Research Coordinator for a Clinical Trials Processing Lab. ...
The Clinical Research Coordinator (CRC) will be responsible for managing the day-to-day activities of a highly innovative portfolio involving participant engagement in cardiovascular and hypertension clinical research. We are an innovative research entity within the Division of Cardiology (Hypertens...
Alcanza Clinical Research (“Alcanza”) is a national, collaborative network of clinical research sites, founded on the mission to accelerate the development of new therapies by reducing barriers to clinical research participation for all. The RA performs clinical, lab, and administrative tasks as nee...
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. ...
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. ...
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...
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. ...
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 ...
Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO). Assist multidisciplinary team in research activities. ...
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 ...
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...
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 RA performs clinical, lab, and administrative tasks as needed for the successful operation of the clinical research site. Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. Clinical Researc...
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...
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 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. ...
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 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...
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 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...
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...