- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a Sr. Investigator as part of the Technical Operations team based in Raritan, NJ.Role ... OverviewThe CAR-T Sr. Investigator will be part of the Technical Operation team and will be responsible to provide specialist knowledge and expertise of cell and… more
- AUROBINDO (Durham, NC)
- …world to live in.Job OverviewAs a key site Quality Employee the QA Investigator will be responsible for assuring that the investigations are conducted and written ... in compliance with all cGMP regulatory as well as facility requirements. This individual will be responsible for:Leading, conducting, writing, reviewing and approving investigations for Deviations and Market Complaints.Assisting SMEs in root cause analysis and… more
- Merck & Co. (Salt Lake City, UT)
- …activities including our Company sponsored trials and our Company Independent Investigator Study Programs as prioritized and requested by our Research Development ... requested by our Research & Development Division's leadership, including our Company's Investigator Study Program (ISP), by acting as the primary liaison to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with Academic Research Organizations (AROs), and meetings with CRO and Investigator Meetings.Support Fair Market Value process in evaluating study budgetsCollect ... to supervisor's attention.Track study metrics such as site start-up, Investigator /site performance, recruitment, regulatory documents, TMF filing and QC activities… more
- Legend Biotech USA, Inc. (Atlanta, GA)
- …scientific meetings including congresses, symposia, advisory boards, and investigator meetings. Interpret and report findings with recommendations for ... research staff who may participate in company sponsored and investigator initiated clinical trials.Demonstration of excellent oral presentation and communication… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …the USOMA Plan. Provides medical review of expanded access programs (EAP) and, investigator -initiated studies (IIS) as part of a US IIS Review Committee, for ... engagement activities with key external stakeholders such as advisory boards, investigator interactions, congress activities, peer to peer discussions with key… more
- City of Spring Hill Kansas (Spring Hill, KS)
- …2 and above may be eligible for consideration as a department investigator . This employee should possess excellent communication and public relations skills. The ... position requires a valid Kansas driver's license. Apply department orders, rules and regulations to police situations; understands and applies legal standards. Operates patrol/unmarked vehicle in a safe and effective manner; inspects vehicle for safe and… more
- Insmed Incorporated (San Diego, CA)
- …regulatory documents (ie, IND submissions, IND Annual Updates, DSUR, and Investigator Brochures) Support enrollment projections and assist with the development and ... implementation of subject recruitment and retention strategies Provide scientific support to the study teams, including:Collaborate with team members in the review and development of Data Management activities including eCRFs, edit checks, report development,… more
- Daiichi Sankyo, Inc. (Minneapolis, MN)
- …and study committee members for DSI clinical research programs, 2) investigator -initiated research study proposals, 3) speakers for DSI Brand Speaker programs, ... 4) advisors for DSI scientific, clinical and marketing advisory boardsGathering customer insights regarding DSI and competitor products to help inform medical and commercial decision-makingEnhanced professional expertise through attendance of select scientific… more
- Insmed Incorporated (NJ)
- …clinical studies.Perform medical monitoring, coding, and data cleaning, and prepare Investigator Alert letters and SAE reports in collaboration with Clinical ... Operations.Ensure the medical integrity of clinical study reports and data interpretation/communication.Author or oversee authorship of clinical sections of regulatory submissions (INDs, briefing books, BLAs, NDAs, etc.) and represent the company at regulatory… more
