- Merck & Co. (Rahway, NJ)
- …of the study protocol as well as preparation and presentation of the clinical supplies information at Investigator Meetings for assigned protocols. - Support ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...(GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full c ompany's Research… more
- Legend Biotech USA, Inc. (Baton Rouge, LA)
- …and their research staff who may participate in company sponsored and investigator initiated clinical trialsDemonstration of excellent oral presentation and ... team. Direct education for healthcare professionals treating oncology patients on clinical data, adverse event management, and mechanism of action for commercial… more
- Eisai, Inc (Nutley, NJ)
- …; tracking certifications and maintain statuses of study team membersAssist with investigator meeting planning, including entering clinical meetings into Eisai ... your profile, we want to hear from you. The Clinical Trial Assistant will support all phases of ...Clinical Trial Assistant will support all phases of clinical study activities (feasibility, start-up, conduct and close-out) under… more
- Genmab (NJ)
- …the drafting and editing of critical documents such as protocols, investigator 's brochures, and clinical study reports.Contribute to Health Authority ... industry. Oncology and immunology experience preferredDemonstrated experience authoring protocols, investigator 's brochures, and clinical study reports. Senior… more
- Northwestern Memorial Healthcare (Chicago, IL)
- …is responsible for serving as a liaison between Northwestern University (NU) clinical research investigator teams (eg, investigator -initiated trials, sponsor ... care of our employees. Ready to join our quest for better? Job Description The Clinical Research Nurse reflects the mission, vision, and values of NM, adheres to the… more
- Merck & Co. (NJ)
- …and goals for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The RMSD serves as a role model for ... with applicable policiesMaintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) for the… more
- Merck & Co. (Chicago, IL)
- …and goals for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies and serve as a role model for other ... (GMSA) strategy, including field standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities.Location: This is… more
- Merck & Co. (Rahway, NJ)
- …Development Team, Global Brand and V&I Outcomes Research leads to define clinical development plans and brand strategies for assigned TAsProvides a solid ... as relevant members to the Product Development sub-teams (Value Evidence, Clinical , Commercial, Publications and Label teams)Aligns medical plans and activities with… more
- Merck & Co. (North Wales, PA)
- …DescriptionThis position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have ... management, communication, and collaboration skills in support of our clinical trials.Job Responsibilities: Responsible for the operational planning, feasibility,… more
- Genmab (NJ)
- …through scientific exchange in a fair and balanced manner and provide clinical /scientific support for Genmab's pipeline.Domestic travel of approximately 50% will be ... regional, national, and global Medical Affairs strategiesProvide insights/feedback on emerging scientific/ clinical data that enhance the value and appropriate use of… more
- BioAgilytix (Durham, NC)
- …a Scientist III to serve as Bioanalytical Project Manager (BPM)/Principal Investigator (PI), overseeing all aspects of bioanalytical studies-including project scope ... we tackle challenges across the spectrum of drug discovery to clinical diagnostics, driving advancements that shape the future of healthcare.Essential… more
- Hackensack Meridian Health (Paramus, NJ)
- …out the research and works under the general supervision of the principal investigator responsible for the clinical trial(s) to which is assigned. ... issues and changes within the protocol. In collaboration with the principal investigator , clinical research coordinator, and clinical team, participates… more
- Eisai, Inc (Cincinnati, OH)
- …Eisai, the company and its hhc mission; b) provide key scientific and clinical information about Eisai's products; serve as a conduit for communication between Eisai ... Product/Therapeutic Area Support to External Stakeholders Act as the primary clinical /scientific resource to Healthcare Providers (HCPs) in the territory for… more
- Taiho Oncology (FL)
- …practitioners on Taiho products and relevant disease states, and facilitation of clinical research. The Sr. Manager, Medical Field integrates clinical /scientific ... Product/Therapeutic Area Support to External Stakeholders: Act as the primary clinical /scientific resource to HCPs in a specified geography for information… more
- The University of Chicago (Chicago, IL)
- …Clinical Research Coordinator (Sr. CRC) is a specialized researcher partnering with the clinical Principal Investigator (PI) and under the direction of the ... Department BSD MED - Hematology and Oncology - Clinical Research Staff - Cluster 3 About the...Hematology/Oncology in the Department of Medicine. While the Principal Investigator is primarily responsible for the overall design, conduct,… more
- Mount Sinai Hospital (New York, NY)
- …in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, ... of the research project, under direct supervision of the Principal Investigator or senior clinical research staff. 2. Assists in the activities related to … more
- Merck & Co. (North Wales, PA)
- …access and identifies value evidence needs to provide strategic input into clinical and market development programs.- Brings strong payer and HTA/reimbursement focus ... report forms, data analysis plans, and final reports/publications.Works with the Investigator Study Program Committee to evaluate outcomes research study protocols… more
- Genmab (NJ)
- …us!The RoleThe Associate Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead for both early ... responsibilities as described below. The Associate Director contributes to clinical development strategies and plans.Responsibilities:Compound/Indication LevelAct as lead and… more
- BioAgilytix (San Diego, CA)
- …Manager II will lead scientific and operational activities in support of preclinical, clinical , and product release studies for our San Diego lab. This role requires ... team(s) developing and validating bioanalytical assays for support of preclinical, clinical and product release studies.Motivating team by inspiring employees to… more
- BioAgilytix (San Diego, CA)
- …studies in biological matrices using LC-MS/MS, supporting preclinical and clinical development across multiple modalities. The remaining 5% will involve ... troubleshoot issues, and ensure timely completion of studies.Serve as Principal Investigator or Study Director for GLP/validation projects, reviewing data, methods,… more
