- Insmed Incorporated (NJ)
- …each other, and for the future of science, we're in. Are you?About the Role:The Clinical Trial Manager will be responsible for the management and oversight of ... services, management of project timelines and deliverables. Key trial management support to the Associate Directors...Leads and coordinates the management and execution of all clinical trial activities in compliance with GCP… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …more about Life at Olympus: https://www.olympusamerica.com/careers . **Job Description** The Sr. Clinical Trial Coordinator (Sr. CTC) will be responsible for ... and primary point of accountability and reconciliation for the Trial Master File (TMF) and the Investigator Site...resolution of data queries under the guidance of the Clinical Research Associate (CRA), Data Management and/or… more
- Caris Life Sciences (Phoenix, AZ)
- …yourself, Caris is where your impact begins.** **Position Summary** A Clinical Trial Specialist-Biorepository provides operational and regulatory support for ... include, but not limited to, study documentation maintenance, leading site onboarding activities, driving site engagement through...have 1-2 years' experience in a Biorepository setting or Clinical Trial setting + Proficient in Microsoft… more
- Stony Brook University (Stony Brook, NY)
- …correspondence with sponsors and IRB in obtaining approvals and maintenance of clinical trial materials and documents. Experience with research informed consent ... Clinical Research Associate II **Required Qualifications...Neurosurgery clinical research trials; collect and submit clinical trial patient data, coordinate patient appointments.… more
- BeOne Medicines (Emeryville, CA)
- …guidelines - Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ... Familiar with industry CTMS and data management systems **Other Qualifications:** - Understands clinical trial processes with a thorough knowledge of ICH and… more
- Merck & Co. (Rahway, NJ)
- …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good … more
- Merck & Co. (Boston, MA)
- …Atherosclerosis, Cardiology Clinical Research, Cardiovascular Diseases, Clinical Development, Clinical Studies, Clinical Trial Designs, Clinical ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
- Merck & Co. (Upper Gwynedd, PA)
- … Clinical Judgment, Clinical Medicine, Clinical Reporting, Clinical Research Management, Clinical Trial Development, Communication, Data Analysis, ... serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology Clinical ...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (North Wales, PA)
- …Engineering or closely related field plus 9 years SAS programming experience in a clinical trial environmentOR a Master's degree (or US equivalent) in Computer ... field plus 7 years SAS programming experience in a clinical trial environment.Requirements:Experience and knowledge in leading...You can apply for this role through the- Career Site (or via the Workday Jobs Hub if you… more
- Merck & Co. (Rahway, NJ)
- …field and relevant experienceRequired Experience and Skills:-- -A deep understanding of the clinical trial process: You can speak the language of protocols, ... Job DescriptionWe are seeking an Associate Principal Scientist to contribute to a pivotal...stewarding these data, you will empower our scientists and clinical teams to make faster, data-driven decisions that propel… more
- Insmed Incorporated (Minneapolis, MN)
- …Clinical Operations, and Medical Affairs Departments. This may include trial site identification, ongoing recruitment motivation, and issue/problem ... strong related experience.Other Pharmaceutical experience - Medical Information, Medical Strategy, Clinical management/ trial experience and 2 years clinical … more
- Insmed Incorporated (St. Louis, MO)
- …Clinical Operations, and Medical Affairs Departments. This may include trial site identification, ongoing recruitment motivation, and issue/problem ... and infectious diseaseOther Pharmaceutical experience - Medical Information, Medical Strategy, Clinical management/ trial experience and 2 years clinical … more
- Aequor (New York, NY)
- …Supporting the development of the patient reported outcomes strategy in a clinical trial setting Literature review and evidence synthesis. Supporting ... Description: Research Associate (Contractor) HTA Value & Evidence, Oncology, Global...the development and execution of deliverables to support early clinical development programs. The position is located at Headquarters… more
- Parexel (Baton Rouge, LA)
- …in Lupus is preferred -Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability ... experience treating rheumatology patients clinically and/or who possess extensive rheumatology clinical trial related experience will be considered for this… more
- BeOne Medicines (San Mateo, CA)
- …healthcare discipline* with minimum of 8 years of combined experience in Feasibility, Clinical Data Analytics, Clinical Trial Management, and Operations ... into actionable insights that drive strategic feasibility decisions, enhance country and site feasibility, and optimize study planning. As the analytics lead, this… more
- Lundbeck (Deerfield, IL)
- …of the R&D and Medical organization to ensure appropriate TPP development specifically clinical trial endpoints. **Leader of Cross-Functional US Teams** + To ... assets in collaboration with appropriate stakeholders. + Work closely with Associate Director, US NPP to increase internal capabilities and deliver evaluation… more
- CSL Behring (King Of Prussia, PA)
- …timely processing of dispense data to update SAP inventory + Manage shipments for Clinical Trial or IIS Programs; ensure compliance of SOPs and Sunshine Act ... impact on the organization. In this role you will report into the Associate Director, Customer Support. **Responsibilities:** + Respond to all inquiries received by… more
- Lilly (Stamford, CT)
- …with a strong working knowledge of the clinical research process + Prior clinical trial site -level or affiliate experience + Prior experience with ... better for people around the world. **Position Summary** : The Associate Director, Clinical Development Trial Lead (CDTL) independently leads the… more
- IQVIA (Washington, DC)
- … clinical trial operations for the firm's clientele.** **Position Overview** **The Clinical Trial Associate (CTA) supports the In-House Clinical ... Research Associate and clinical Trial Manager to ensure optimal management of essential documents...for site use.** **Handle, distribute and track clinical trial supplies (non-IP) for site… more
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