- BioAgilytix (Durham, NC)
- …fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You'll gain experience with a variety ... a Scientist III to serve as Bioanalytical Project Manager (BPM)/Principal Investigator (PI), overseeing all aspects of bioanalytical studies-including project scope… more
- Merck & Co. (North Wales, PA)
- …level plans/timelines, country/site selection, site materials, system updates, investigator -meeting planning, communication plans, preparation of status update ... Outlook, etc.)Education/Experience: Bachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical field experience/ Master's… more
- Genmab (NJ)
- …you join us!The RoleAre you ready to make a meaningful impact in oncology drug development and be part of a dynamic, collaborative team that values innovation, ... the drafting and editing of critical documents such as protocols, investigator 's brochures, and clinical study reports.Contribute to Health Authority briefing… more
- Merck & Co. (Boston, MA)
- …definitive/Good Laboratory Practice (GLP)], serving as a contributing scientist/principal investigator on toxicity studies, and executing PK/TK strategies to support ... for all TK-related issues pertinent to the development of assigned drug candidates and closely interact with toxicology study directors, project representatives,… more
- Merck & Co. (Rahway, NJ)
- …establish a consolidated , visible forecast for all study product needs (Bulk Drug Product and Clinical Finished Goods).- - Responsible for authoring clinical supply ... well as preparation and presentation of the clinical supplies information at Investigator Meetings for assigned protocols. - Support the collection of clinical suppl… more
- Genmab (NJ)
- …conducting trial result meetingsReview and approve the CSRAttend trial and investigator meetings if/as neededCollaboration with Genmab Global Drug ... scientific and technical progress within the field of biostatistics in drug development and advise of new methodologies that may support innovation… more
- Legend Biotech USA, Inc. (Baton Rouge, LA)
- …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 trialsDemonstration of excellent oral presentation and communication… more
- Merck & Co. (North Wales, PA)
- …cost of diseases, unmet medical need, patient reported outcomes (PRO) and the value of drug therapy as outlined in the OR planning process and generates data on a ... report forms, data analysis plans, and final reports/publications.Works with the Investigator Study Program Committee to evaluate outcomes research study protocols… more
- Merck & Co. (Rahway, NJ)
- …(CMO) sites that manufacture active pharmaceutical ingredients (API), biologics, vaccine drug substances and finished products. As Director, you will support Quality ... Experience working for a health authority as an inspector, investigator , compliance officer, reviewer, or assessorExperience creating or assessing remediation… more
- Genmab (NJ)
- …the primary point of contact and facilitator for all aspects of investigator sponsored trials (ISTs), from submission, review and approval, through study ... resulting in a proprietary pipeline including bispecific T-cell engagers, antibody- drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced… more
- BioAgilytix (San Diego, CA)
- …fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You'll gain experience with a variety ... and prepare SOPs.Fulfill the role of Bioanalytical Project Manager (BPM)/Principal Investigator (PI) for all assigned clients and studies.Lead regularly scheduled… more
- Eisai, Inc (Nutley, NJ)
- …planning. Research Support Facilitate review and follow up of submitted Investigator -Initiated Studies (IISs) and assist with Eisai sponsored trials.Serve as primary ... Strong broad-based scientific and pharmaceutical knowledge.Clinical trial development and drug launch experience is strongly preferred.Knowledge of treatment guidelines,… more
- Taiho Oncology (FL)
- …as defined in the pharmacovigilance SOPs related to medical inquiries and drug safety information. Use medical affairs plans to develop and align the ... In collaboration with Medical Affairs personnel support data generation Investigator -Initiated Trials (IITs) and HCP initiated projects. Facilitate the review… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …(eg, Project Team, Alliance, Ad hoc, Steering committee, Ad board, workshops, Investigator & Governance meetings). This includes, but is not limited to, the ... experience as a project administrator or similar role in a pharmaceutical drug development environment required Travel:Ability to travel up to 5% Daiichi Sankyo,… more
- Mastercard, Inc. (New York, NY)
- …and governments realize their greatest potential. Title and Summary Senior Investigator , Global Rules Program About the Opportunity: Mastercard's Franchise Brand ... part time) employees generally include: insurance (including medical, prescription drug , dental, vision, disability, life insurance), flexible spending account and… more
- StateJobsNY (Albany, NY)
- …(OSI) is seeking qualified candidates for consideration to serve as an Investigator in one of its five divisions with cross-over and collaboration among ... serious injury or death, threats of violence, gun and drug distribution and possession, contraband smuggling, and criminal organizations...for several openings across New York State as an Investigator in one of OSI's divisions. The OSI division… more
- Kymera Therapeutics (Watertown, MA)
- …to the preparation and review of clinical study documents including the Investigator Brochure, Investigational New Drug Applications (IND), study protocols, ... clinical study reports, applicable sections of New Drug Applications (NDA) and or Marketing Authorization Application (MAA), updates to the IND, NDA and other safety… more
- NYULMC (New York, NY)
- …performs study coordination tasks under the direction of the principal investigator /treating investigator , under the supervision of CTO management/leadership and ... and safe screening research visit(s) under the direct supervision of the PI/ investigator . Supports a safe and compliant eligibility process, following internal and… more
- Miltenyi Biotec (Waltham, MA)
- …data acquisition strategy, methodology, and approach for safety evaluations. Serve as drug safety representative on clinical trials with CRO participation. Lead or ... risk management plans to mitigate safety concerns associated with a drug , including developing safety communication strategies. Support preparation of registrational… more
- Eli Lilly and Company (Boston, MA)
- …Overview: ExploR&D, a Division of Lilly Research Laboratories, is a drug development organization with a mission to catalyze the biotechnology ecosystem. ... As a multidisciplinary team of highly experienced drug developers, we seek to advance investigational medicines for external sponsors with speed and efficiency.… more
