- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director, Value & Implementation (V&I), Global Medical and Scientific Affairs (GMSA) is accountable for the development and execution of ... scientific & medical affairs plans for Ophthalmology). They build and lead...with V&I Outcomes ResearchSupports the Investigator-Initiated Study programLeads talent review process and demonstrates follow-through on Development Plans for… more
- Merck & Co. (Rahway, NJ)
- …to ensure a thorough understanding of the science behind the medicine and review further unmet medical needs to support collaboration to further differentiate ... Job DescriptionOur Medical Affairs team advances patient care by engaging...-We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco… more
- Merck & Co. (Rahway, NJ)
- …and performance evaluation. This allows the organization to continue advancing medical innovation and improve lives. -Position Description: The main responsibilities ... risk and present results to Senior Management. Perform a review of our Company's top key products in order...-We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco… more
- Merck & Co. (Rahway, NJ)
- …reporting and performance evaluation. This allows the organization to continue advancing medical innovation and improve lives. - As the Company's portfolio continues ... and guidance to support decision making across vendor selection, contract negotiation & review and risk assessments and will be the primary point of contact to… more
- Merck & Co. (Rahway, NJ)
- …their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to set tactical and strategic direction on programs ... development activities including engineering design, engineering analysis and testing, medical device design controls, risk management, test method/fixture development,… more
- Merck & Co. (Rahway, NJ)
- …team, device technical operations, and manufacturing sites.Travel to OEMs to review equipment design, conduct line trials including FAT and report project ... 820, ISO 13485, ISO 14971 etc.) -and industry standards related to medical device manufacturing is a plus.Prior experience in glass container handling/assembly and… more
- Merck & Co. (Rahway, NJ)
- …experience among communicators to drive business objectives across sites. Development, review and approval of strategic communications materials for the Executive ... Minimum of 10 years of experience in pharmaceutical, healthcare, medical tech or biotech communications , with a strong...-We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco… more
- Merck & Co. (Rahway, NJ)
- …robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our Company's success is backed by ethical integrity, forward ... tools, and requirements for all dosage forms (liquid, lyo, drug-device combinations) Review and approval of data and technical documentsAbility to recruit, select,… more
- Merck & Co. (Rahway, NJ)
- …nomenclature data into a centralized databasePerforming data integrity review activities, including proofreadingDeveloping rules to ensure data qualityContributing ... and developing taxonomies, reference data or controlled vocabulariesFamiliarity with medical devicesExperience with FAIR principles and other standardsExperience writing… more
- Merck & Co. (Rahway, NJ)
- …a Global Labeling Lead, you will guide cross-functional teams in the creation, review , and approval of Core and Local Labeling documents.You will be responsible for ... of labeling experience or relevant pharmaceutical industry experience (eg, Medical Affairs, Regulatory Affairs, Clinical, Pharmacovigilance).Current Employees apply HERE… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …standing by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records . Qualifications Doctoral degree required At least ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...in region to Director including budget expenditures as directed Records all activities within a customer response management system… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …for budget records and prepares documents required for the budget review processes Develops requests for proposals; evaluates and provides input into vendor ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...pertinent factors based on the project; and coordinates legal review of finalized contract; Manages vendors to ensure the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Regulatory Intelligence (PVRI) and dissemination across CSPV stakeholders. Participates in the review and management of monthly, quarterly, and ad hoc PVRI reports… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... projects, assists with corporate business filings, and legal technology projects.- Records Management: Provide general support regarding the corporate records … more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …integrityExecutes, owns, assesses and participates in the creation, revision and review of change controls, SOPs, and other documentationParticipates in authoring ... authoring and executing documentation including but not limited to: Batch Records , SOPs, Work Instructions, CQV protocols.Experience with TrackWise, Comet, CMMS,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Includes the following but not limited to: assist with lab cleanings, logbook review , request of logbooks, filing training records , assist with lab ... on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability,… more
- MTA (Brooklyn, NY)
- …TWU Responsibilities: This position performs day-to-day responsibilities of the Medical Records Unit (MRU), which includes: extensive review of employees' ... Administrative Assistant Series - Medical Records Unit (OHS) Job ID: 10033 Business Unit: MABSTOA Location: Brooklyn, NY, United States Regular/Temporary:… more
- Molina Healthcare (New York, NY)
- …with physician and member interventions and incentive efforts as needed through review of medical records documentation. **Job Qualifications** **REQUIRED ... **Job Description** **Job Summary** Molina's HEDIS/Quality Improvement Sr. Medical Records Collector is a team member with several years experience in working… more
- MTA (Brooklyn, NY)
- Staff Analyst Series - Medical Records Unit (OHS) Job ID: 10294 Business Unit: MABSTOA Location: Brooklyn, NY, United States Regular/Temporary: Regular ... Posted: Jan 29, 2025 Description Job Information: Title: Staff Analyst Series - Medical Records Unit (OHS) Opening Date: 1/27/2025 Closing Date 02/10/2025… more
- MTA (Brooklyn, NY)
- Staff Analyst Trainee Series - Medical Records Unit (OHS) Job ID: 10295 Business Unit: MABSTOA Location: Brooklyn, NY, United States Regular/Temporary: Regular ... Jan 29, 2025 Description Job Information: Title: Staff Analyst Trainee Series - Medical Records Unit (OHS) Opening Date: 1/27/2025 Closing Date 2/10/2025… more
