- Merck & Co. (Rahway, NJ)
- …Material(s):n/aRequired Skills:Adaptability, Adaptability, Business, Business Risks, Change Management, Clinical Development, Clinical Research , ... Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full Company's Research & Development… more
- Merck & Co. (Rahway, NJ)
- …managing the 'end-to-end' integrated clinical supply chain across the full c ompany's Research & Development Division portfolio of clinical trial s .- GCS is ... within the business.-- - - Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM).... - Interacts with key partner organizations such as clinical development, regulatory , quality and other supply… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disordersJob Summary: The Regulatory Process Manager will be a key member of the Global ... Regulatory Affairs (GRA) Process Excellence & Analytics function, responsible...Regulatory Affairs and cross-functional teams (eg, Quality, CSPV, Clinical Operations, Clinical Development, RA CMC) to… more
- Merck & Co. (North Wales, PA)
- …and key strategic engagements. This includes the ability to:Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability ... (eg, ICF documents / amendments); Partners with the Study Manager on study deliverables.Ensuring CRF design supports data collection...Adaptability, Clinical Data, Clinical Operations, Clinical Outcomes, Clinical Research , … more
- Merck & Co. (Rahway, NJ)
- …tactical/scientific mentorship to other clinical scientists. Core Skills Solid knowledge of clinical research regulatory requirements (e . g . , GCP ... . , ICF documents/ amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data... Clinical Data, Clinical Data Interpretation, Clinical Operations, Clinical Research , … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Interactions: Leads US FDA/EU EMA interactions with support from higher-level manager . Regulatory Knowledge: Demonstrates expert knowledge of US/EU regulatory ... focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.Summary: This position manages… more
- Merck & Co. (North Wales, PA)
- …for managing any study specific partners and/or vendors.Core Skills: Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to ... Driving License:NoHazardous Material(s):n/aRequired Skills:Adaptability, Adaptability, Clinical Data, Clinical Operations, Clinical Research , Clinical… more
- Merck & Co. (North Wales, PA)
- …collaborations, and key strategic engagements. This includes the ability to:--Strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) ... the strategy and leads the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to demonstrate your… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …relationships with key stakeholders within CSPV and external functions including Clinical Development, Research Development, Regulatory Affairs.Facilitate ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary: Manage… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Pharmaceutical industry, with involvement in regulated clinical trials, clinical safety, pharmacovigilance included regulatory document reviewMust have at ... providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders....years proficiency in ICH GCP Guidelines, US and European regulatory requirements for the conduct of clinical … more
- Merck & Co. (North Wales, PA)
- …Vice President in BARDS and will work collaboratively with other leaders in Clinical Development and Global Regulatory Affairs.--The AVP provides leadership and ... Job DescriptionIn Biostatistics and Research Decision Sciences (BARDS), a distinguished department within our renowned Research and Development division,… more
- BioAgilytix (Durham, NC)
- …is seeking a Scientist III to serve as Bioanalytical Project Manager (BPM)/Principal Investigator (PI), overseeing all aspects of bioanalytical studies-including ... we tackle challenges across the spectrum of drug discovery to clinical diagnostics, driving advancements that shape the future of healthcare.Essential… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary: The Senior ... Collaboration and partnership with other functions and stakeholders in supporting clinical trial monitoring and execution through RBQM activities. Accountable for… more
- Eisai, Inc (Nutley, NJ)
- …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... speakers and related aspects of speaker programsCollaborate with Promotional Program Manager for speaker usage and issuesOffer feedback on nominating new speakers… more
- Medix (Grand Rapids, MI)
- Clinical Research Nurse Supervisor Are you ready to be at the forefront of changing lives for the better? As a member of our global team, you'll contribute to ... clinical competency and may be required to perform clinical research -specific patient care tasks as needed...activities to ensure adherence to protocol, patient safety, and regulatory compliance. Partner with the Manager and… more
- Insight Global (New York, NY)
- …& Experience Bachelor's degree in life sciences or related field 5+ years of clinical research project management experience Experience with clinical trial ... A leading healthcare system is seeking a fully remote Project Manager . As a Project Manager for cohort Site Management, you will manage the day-to-day operations… more
- Project Renewal (New York, NY)
- Title: Clinical Practice & Training Manager Reports to : Sr. Director of Clinical Development & Training Schedule: Monday to Friday; Hybrid schedule. ... supervision of the Senior Director of Clinical Development & Training, the Clinical Practice & Training Manager leads the design and implementation of… more
- Abbott (Minneapolis, MN)
- …location for our Electrophysiology division. As a manager , the function of a Manager Regulatory Affairs is to combine knowledge of scientific, regulatory ... and get on with their lives. The Opportunity The Regulatory Affairs Manager will work on-site at...regulatory submission to authorities. Evaluate risk of and regulatory solutions to product and clinical safety… more
- Arrowhead Pharmaceuticals (San Diego, CA)
- …documentation to ensure regulatory compliance and conformance with existing regulatory applications and approvals Research and analyze regulatory ... Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that...candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San… more
- Mount Sinai Hospital (New York, NY)
- Job Description Job Title: Wound Care Clinical Program Manager , NP - Wound Care Center, Mount Sinai Hospital, Full-time - Day The Clinical Program Manager ... clinical orientation, competency assessment and interventions in the assigned clinical program of designated nursing staff within the Medical Center. This… more
