The Certified Mobile Research Nurse is a Registered Nursing per diem/PRN position for PCM Trials. You’ll work cooperatively with Clinical Project Managers, Coordinators, and site personnel to complete visits and submit accurate source documentation. No research experience required, on the job ...
Possess good understanding and working knowledge of ICH guidelines, Good Clinical Practices (GCP), PhRMA code, FDA CFR, clinical research ethics, HIPAA and patient privacy laws, and other relevant, local regulatory requirements. Regional Clinical Research Monitoring. Ensures that the conduct of clin...
Responsible to ensure the overall success of the designated Clinical operations/ monitoring projects. ...
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum of 2 years’ experience in monitoring pharmaceutical industry clinical trials. Have an in-depth knowledge of Good Clinical Practice, ICH g...
CHDI’s Clinical Team oversees a portfolio of projects aimed at understanding the natural progression of HD disease, developing the best biomarkers and outcome measures for use in clinical trials, finding ways to expedite and improve the execution of clinical trials, paving relevant regulatory ...
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. To drive continued success in this exciting clinical research ...
The Medical Evidence Generation (MEG) Clinical Research Collaborations team actively bridges Bristol Myers Squibb to the best external science through collaborations with external research entities and networks of practicing clinicians. The Director, Clinical Research Collaborations Lead, will co-le...
Senior Clinical Research Associate. 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 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...
SOPs, informed consent forms, monitoring plans, communication plans, tracking tools, and other project tools as needed draft, review and negotiate changes in informed consent forms evaluate, select, and manage CROs, contractors and other outside vendors anticipate areas of risk, and plan and impleme...
Clinical Research Scientist as indicated for ongoing clinical trial-related activities to provide high-quality and timely deliverables. Assists to execute the clinical trial in alignment with the clinical development plan (CDP). Clinical research experience preferred. This position may serve in a le...
Clinical Research Associate (CRA) III. As a Clinical Research Associate (CRA) III, your responsibilities:. Strong knowledge of Good Clinical Practice (international quality standard for human clinical trials) and local regulations. Conduct clinical trials of pharmaceuticals. ...
Use medical and clinical expertise in design, implementation and monitoring of clinical studies (from Phase 1 to 4) in a team setting. Reports to the Executive Director- Clinical Research & Development. Clinical study management: Provide regional medical & scientific input on trial outlines, trial p...
This position is responsible for working with the physicians within Clinical Development to provide clinical research support for programs as assigned by phase or therapeutic area. Development of protocols for clinical studies. Contribute to the development of program strategy for assigned compounds...
The Medical Evidence Generation (MEG) Clinical Research Collaborations (CRC) team actively bridges Bristol Myers Squibb to the best external science through collaborations with academic institutions and networks of practicing clinicians. The Director, CRC Lead, Hematology/Cell Therapy, will co-lead ...
This position contributes to the implementation of the global development strategy, leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds in various stages of clinical development. This may include clinical trial implementation, and oversight of all aspect...
As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a mini...
This position serves as a key role in the effective implementation of the global development strategy leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds in various stages of clinical development (including clinical trial implementation, and oversight of...
We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II. ICON plc is a world-leading healthcare intelligence and clinical research organization. Cond...
Clinical Research Associate (CRA) III. As a Clinical Research Associate (CRA) III, your responsibilities:. Strong knowledge of Good Clinical Practice (international quality standard for human clinical trials) and local regulations. Conduct clinical trials of pharmaceuticals. ...
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 Early Clinical Development Senior Clinical Research Associate will have relevant Phase I experience, responsible for conducting monitoring activities for one or more client sponsored studies. CRA functions as a member of the clinical study team and performs study monitoring according to Good Cli...
May act, in concert with senior clinical personnel, as the company spokesperson regarding publication of clinical research findings. Contributes to the interpretation, reporting and preparation of oral and written results of product research in concert with senior clinical personal, in preparation f...
Sourcing category/group experience in one or more of the following is preferred: Market Research, Data & Analytics, Clinical Operations Pharmaceutical industry experience helpful, but not required Ability to exert influence on the overall objectives and goals of the department Ability to multi-task ...
We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II assigned to Early Development trials (Phase I). ICON plc is a world-leading healthcare intell...