- Arvinas (New Haven, CT)
- …and external) on study design elements and endpoints + Contribute to the clinical portion of investigator brochures review for consistency and applicability + ... and medical literature to support document development, such as the investigator brochure, protocol design, clinical study report, competitive assessments,… more
- Stony Brook University (Stony Brook, NY)
- …and administering of research, testing, lab study agreements, including sponsor or investigator -initiated clinical trials, supported by a variety of sponsors. ... in the process of negotiating agreements. Assist PIs in formulating budgets for investigator -initiated clinical trials or other research agreements and act as… more
- Parexel (Cheyenne, WY)
- …Provide necessary support to cross-functional teams including Start up, Global Clinical Operations, Investigator Payments, Business Development and Feasibility + ... Site Contract Leader is responsible for overseeing the site contracting process for clinical trials. The Site Contract Lead will manage the site contracting process… more
- BeOne Medicines (San Mateo, CA)
- …regional study vendors + Manages regional study budgets + Works closely with Clinical Business Operation on investigator fees, site payment issues and patient ... readiness quality, within agreed timelines and budget + Leads the regional clinical operations team (including oversight of external partners working on the regional… more
- Parexel (Bismarck, ND)
- …in Lupus is preferred -Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability ... with feasibility leaders, solution consultants + Participate in team project and investigator meetings + Provide training of study teams on TA indication and… more
- Organon & Co. (Savannah, GA)
- …and research including facilitation of research collaborations such as investigator -initiated trials and collaboration with Clinical Development colleagues ... The Medical Science Liaison is a field-based professional with scientific, clinical and therapeutic area expertise responsible for providing medical and scientific… more
- CSL Behring (King Of Prussia, PA)
- …the Clinical Development Plan (CDP), the Project Strategy Document (PSD), Investigator Brochures (IB), Clinical Study Protocols (CSP), Informed Consent Forms ... limited to: the TPP, PSD, CDP, Study Concept Scenarios, Study Outlines, the Investigator Brochure (IB), Clinical Study Protocols (CSP), Master Informed Consent… more
- CSL Behring (King Of Prussia, PA)
- …the Clinical Development Plan (CDP), the Project Strategy Document (PSD), Investigator Brochures (IB), Clinical Study Protocols (CSP), Informed Consent Forms ... worldwide. Could you be our next Senior Director, Global Clinical Program Lead, Cardiovascular? The job is in our...be accountable for the design and execution of the clinical strategy to support the development of a medicine,… more
- Parexel (Dover, DE)
- …client in making budget and contractual decisions against the impacts to client clinical trial timelines + Follow client processes to develop, negotiate, track and ... execute global clinical study agreements with institutions and investigators participating in...study agreements with institutions and investigators participating in sponsored clinical trials + Work with partners to develop and… more
- Children's Hospital Los Angeles (Los Angeles, CA)
- …Matters.** **Overview** **Schedule:** Day Shift **Purpose Statement/Position Summary:** The Clinical Research Assistant assists Principal Investigator with the ... care that is personal, convenient and empowering. Our scientists will work with clinical experts to take laboratory discoveries and create treatments that are a… more
- Parexel (Charleston, WV)
- …for a wide range of documents, including but not limited to investigator 's brochures, clinical study protocols and reports, integrated summaries, literature ... comply with International Committee on Harmonization guidelines, Sponsor SOPs, Good Clinical Practices, and Good Publication Practices. As a study team member,… more
- Terumo Medical Corporation (Somerset, NJ)
- …clinical trial support to sites/investigators that are participating in the clinical research and participate in investigator launch meetings. + Regulatory ... and scientific support for the organization that includes Medical Affairs, Clinical Operations, Sales, Marketing, Regulatory Affairs, to ensure maximum exchange of… more
- Parexel (Carson City, NV)
- …for a wide range of documents, including but not limited to investigator 's brochures, clinical study protocols and reports, integrated summaries, literature ... documents comply with International Committee on Harmonization guidelines, SOPs, Good Clinical Practices, and Good Publication Practices. As a study team member,… more
- BeOne Medicines (Emeryville, CA)
- …and tactical/operational plans aligned to commercial and regulatory objectives. + Clinical trial patient and investigator recruitment experience + Validated ... **General Description:** As the Regional Strategic Feasibility Lead within Global Clinical Operations (GCO), you will play a vital role in collaboration with the… more
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of ... the globe. **Exciting Opportunity** : We're looking for a Clinical Trials Nurse to join our inpatient team! In...and patient/ family support. + Collaborate with the principal investigator to review new protocols from a nursing perspective… more
- Seattle Children's (Seattle, WA)
- …research team with in the organization, implementation and completion of clinical research trials. Maintain regulatory documents; assist the Principal ... Investigator in the planning of protocol implementation and site...implementation and site initiation visits and routine monitoring of clinical studies. Along with the PI, ensure that research… more
- CSL Behring (King Of Prussia, PA)
- …days a week. You will hold work closely with the CDT Lead and other Clinical Representatives in performing delegated tasks in support of the clinical development ... project needs. **Main Responsibilities:** 1 Contribute to the scientific development of clinical programs and individual clinical studies in alignment with the… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …about Life at Olympus: https://www.olympusamerica.com/careers . **Job Description** The Sr. Clinical Trial Coordinator (Sr. CTC) will be responsible for supporting ... the clinical project team during all stages of a ...reconciliation for the Trial Master File (TMF) and the Investigator Site File (ISF). + Manages the tracking, review,… more
- Teleflex (Minneapolis, MN)
- …with team, department, and study-related projects as requested, including audits, investigator meetings, training, etc. o Interfaces with Clinical , Regulatory, ... Regional Clinical Research Associate (REMOTE) **Date:** Nov 8, 2025...patients' lives. **Position Summary** **TRAVEL REQUIRED: 70%** The Regional Clinical Research Associate will be responsible for conducting on-site… more
- Stony Brook University (Stony Brook, NY)
- …University's Renaissance School of Medicine (RSOM) is seeking applications for a clinical pathology faculty member at the Assistant, Associate, or Full Professor ... (Clinician Educator track) to provide laboratory director oversight for the clinical microbiology laboratory section of the Stony Brook University Hospital's… more
