- Merck & Co. (Rahway, NJ)
- …cost estimates requested by Product Development Teams . - Responsible for authoring clinical supply documentation in support of labeling and packaging activities ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...as well as supply chain documentation to support critical CMC activities. - - Support… more
- Merck & Co. (North Wales, PA)
- …Material(s):Required Skills:Business Development, Business Development, Business Management, Clinical Documentation , Clinical Investigations, ... Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical... Clinical Judgment, Clinical Reporting, Clinical Research, Clinical Trial Documentation ,… more
- Merck & Co. (Omaha, NE)
- …the right time. -We are seeking a Growth and Improvement minded Associate Specialist, Logistics who can help drive our Strategic Operating Priorities.Strategic ... SummaryThe Associate Logistics Specialist will be responsible for export of...shipping metrics. The successful candidate will ensure that all documentation for the department has been completed accurately and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJoin Our Team as an Associate Principal Scientist/ Associate Director in Biologics Drug Substance Commercialization!Are you ready to make a ... in and/or spearhead cross-divisional technical teams focused on late-stage clinical process development, characterization, and technology transfer of biopharmaceutical… more
- Eisai, Inc (Exton, PA)
- …difference. If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading and ... new products in development through their lifecycle (Preclinical through phase III clinical development) at the Biologics Pilot Plant as well as supporting… more
- Merck & Co. (Durham, NC)
- …with Microsoft Office (Excel, Word, PowerPoint)Excellent planning, organizational, documentation , presentation and communication skillsAbility to work in ... DayValid Driving License:NoHazardous Material(s):n/aRequired Skills:Business, Business Processes, Capital Planning, Clinical Supply Chain Management, Communication, Customer-Focused, Data Analysis, Financial… more
- Genmab (NJ)
- …as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and ... we would love to have you join us!The RoleThe Associate Director acts as a statistical expert supporting the... Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead… more
- Insmed Incorporated (Los Angeles, CA)
- …Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director Medical Science Liaison will develop and maintain professional ... assigned budget parametersIs accountable for the accurate and timely documentation of all activitiesIdentify Medical Experts, consultants, investigators, and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …project. This position prepares trainings, supports CAPA investigations, case review, documentation reviews in collaboration with the ICSR management and CRO/Vendor ... drug coding conventions (MedDRA, WHO-DD). preferredExtensive knowledge of FDA regulations, clinical and safety databases, preferredFamiliarity with Good Clinical … more
- Merck & Co. (Rahway, NJ)
- …aiding technology development, and supplying Active Pharmaceutical Ingredient (API) for clinical use and drug product development. This will involve handling of ... of the facility.Ensure facility readiness with respect to cleaning (including documentation and execution), dummy run and batch execution, building housekeeping, and… more
- Merck & Co. (Rahway, NJ)
- …aiding technology development, and supplying Active Pharmaceutical Ingredient (API) for clinical use and drug product development. This will involve handling of ... - Ensure facility readiness with respect to cleaning (including documentation and execution), batch execution, building housekeeping, and consumable inventory.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …responsible for the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment. Job duties will be ... Operations.RequirementsH.S. Diploma with relevant experience required; or Certificate or Associate 's degree in a scientific or health services field preferred,… more
- Pharmaceutical Research Associates, Inc (New York, NY)
- Overview As a Senior Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organization, powered by ... experience. A licensed healthcare professional (eg, RN) is also acceptable. An experienced Clinical Research Associate with 5+ years of clinical monitoring… more
- Protara Therapeutics, Inc. (New York, NY)
- …to meet their choline needs via oral or enteral routes. Job Overview: The Clinical Trial Manager (CTM)/ Clinical Research Associate is responsible for ... (CRO) clinical trial services, with a primary focus on ensuring quality Clinical Research Associate (CRA) monitoring and data integrity across all programs.… more
- Nurix (San Francisco, CA)
- …a new script to outmatch disease. Responsibilities and Duties: The Senior Manager/ Associate Director of Clinical Quality Assurance Auditor is responsible for ... and procedures accordingly. Accountable for the QA review of clinical trial documentation and documents submitted to...for the QA review of clinical trial documentation and documents submitted to regulatory agencies. Responsible for… more
- Mount Sinai Hospital (New York, NY)
- Job Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including ... on time and budget. Collect, reviews and files all clinical study documentation for assigned trial(s) and...studies as a clinical trial assistant or clinical research associate is highly desirable. About… more
- Denver Health (Denver, CO)
- …supervision performs concurrent and retrospective reviews as requested by the Clinical Documentation Integrity Manager or Director. Responsible for selected ... summarizes data, establish facts and draw conclusions. Possesses knowledge of clinical documentation and coding concepts, DRG assignments, Inpatient Prospective… more
- Mass General Brigham (Boston, MA)
- …BWH committees related to SRNA education. Directly communicate with the Nursing Clinical Coordinator to ensure proper on-boarding and documentation for all ... of the SRNA educational program. The Assistant SRNA Program Director provides clinical and didactic support to the School of Nurse Anesthesia student population… more
- Catholic Charities Diocese of Paterson (Paterson, NJ)
- …in our Residential/Outpatient Treatment Facilities and Community Programs. Residential Life Associate Part Time Schedule per week: 4:00pm -12:00am (Saturday and ... the agency as assigned Supervise in-house client visits when assigned Ensure all documentation is included in the client's physical chart or Electronic Health Record… more
- Volastra Therapeutics (New York, NY)
- COMPANY Volastra Therapeutics, Inc. is a clinical -stage oncology biotech company based in New York City, pioneering novel approaches to treating cancer by targeting ... 2019, Volastra has grown to support ongoing discovery efforts and a growing clinical organization. Our lead pipeline programs focus on two distinct inhibitors of… more
