- Merck & Co. (Rahway, NJ)
- …ONSITE 3 DAYS PER WEEK)The Submissions Content Source Management Business Operations Lead is expected to understand the end-to-end regulatory submission process. The ... and finalization, and feed to the Submissions Assembly team. The Business Operations Lead should be able to understand the various source area processes and apply… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent) Our company's Device Product & Process ... with applicable regulatory, quality, company, and customer requirements.-This position will lead cross-functional development teams within and external to Device… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …medical/clinical queries from health authorities. Leadership and Collaboration: Lead cross-functional teams in clinical development , medical affairs, and ... OverviewThe Respiratory Clinical Development Medical Lead will oversee the...new drug or 505(b)(2) applications. This role involves strategic leadership in clinical trials, clinical sciences, medical monitoring, target… more
- Cipla (Fall River, MA)
- Job Title QA QMS Associate Organization Name InvaGen Pharmaceuticals, Inc. Location 927 Currant Rd, Fall River, MA Shift General (8:30AM - 5:00PM) Employment Type ... employee discounts, and other benefits. Purpose The QA QMS Associate position is an individual contributor role and a...are not limited to the following: Assist in the development , implementation, and maintenance of the QMS in line… more
- Aequor (Aliquippa, PA)
- …and execute the on-site operations strategy in partnership with 3PL local leadership , manufacturing sites, planning, and transportation teams. Lead and oversee ... Prepare for and support internal and external regulatory inspections and audits. Lead the development , revision, and lifecycle management of Standard Operating… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …across analytics teams.Responsibilities- Data-Driven Insights Reporting and trend analytics: Lead the development and implementation of robust analytics ... areas centered around rare diseases and immune disorders. Summary The Associate Director, Global Oncology Medical Affairs, Medical Analytics will be responsible… more
- Eisai, Inc (Bethesda, OH)
- …through in neurology and oncology, with a strong emphasis on research and development . Our history includes the development of many innovative medicines, notably ... your profile, we want to hear from you. The Associate Director of Global Submission Management (GSM) is responsible...primary liaison between R&D functions, acting as the submission lead for designated global applications (eg, INDs, NDAs, MAAs,… more
- Merck & Co. (Rahway, NJ)
- …people and animals.- Within the Animal Health Division, we are seeking an Associate Director, Customer Operations, to provide strategic leadership that elevates ... to the Executive Director of Business Operations, this individual will lead a team that will champion cross-functional process improvements, project execution,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …ensure accurate media reporting Leads communications excellence activities that contribute to leadership development within the USO LT via media training, ... approaches to: Corporate Reputation & Brand; Commercial Communications; Enterprise & Leadership Communications; and Digital Channels & Content. We provide objective… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Quality Associate Director/GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, encompassing the ... full scope of site operations.- Collaboration is required with site leadership , regional compliance leadership and Divisional Quality Assurance to elevate site… more
- Merck & Co. (South San Francisco, CA)
- …to our Company's biologics, drug conjugates, and novel modality discovery and development pipeline. The Associate Principal Scientist will be primarily discovery ... Responsibilities:Project-team representative for biologics or other modality drug discovery and development . Contribute to overall team strategy and lead the… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …reward hard work and dedication with opportunities for continuous learning and personal development . Are you ready to maximize your potential with us? The Position ... Manages the entire pre-deal evaluation to contract development , negotiation (Deal to Contract) process for assigned channels...GPOs) and other area/regional accounts. Acts as PCOR Account Lead responsible for leading company response from Deal to… more
- Merck & Co. (North Wales, PA)
- …target in ulcerative colitis (UC) and Crohn's disease (CD).- -- The Associate Director, US Payer Marketing, Immunology, is responsible for developing and ... market access strategies and solutions across the immunology pipeline and business development targets.- The individual will collaborate across functions in the … more
- Merck & Co. (Rahway, NJ)
- … Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project ... provide tactical direction and partner with the DSCS Digital Leadership Team to drive the execution and management of...the broad guidance of the DSCS Digital Program Mgmt Lead , the Associate Director, DSCS Digital Project… more
- Eisai, Inc (Dallas, TX)
- …you. The Associate Director, Access and Reimbursement (AD ARM) will lead the Eisai Access and Reimbursement Managers (ARMs), Eisai's field-based access and ... and oncology, with a strong emphasis on research and development . Our history includes the development of...Reimbursement, the AD ARM will be responsible for the leadership , direction, and management of a team of ARMs;… more
- Formation Bio (New York, NY)
- …and AI driven pharma company differentiated by radically more efficient drug development . Advancements in AI and drug discovery are creating more candidate drugs ... because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach… more
- Cipla (Fall River, MA)
- Job Title : QA Document Control Associate FLSA Classification : Full-Time, Professional Work Location : Fall River, MA Work Hours: General Shift: 08:30 AM - 5:00 PM ... based on business needs) Reports To : QA QMS Lead Salary Range : $64,272 - $77,662 PURPOSE The...: $64,272 - $77,662 PURPOSE The QA Document Control Associate in a pharmaceutical environment is responsible for managing… more
- Insmed Incorporated (NJ)
- …in the US utilizing regionally based scenarios, cases, etc. For locally unique needs, lead development of programs. Couple skills development with scientific ... medical new hires within assigned therapeutic areas.Live and Virtual Training Sessions - Lead the agenda development , logistics, and session planning for live… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of emerging data (internal or competitive), such as congress updates and development program highlights.- Provides medical leadership in interactions with key ... other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director Global Medical Affairs Oncology (GMA), under the direction of… more
- Merck & Co. (Rahway, NJ)
- …Pharm Sciences colleagues.-Recommends and executes programs of value to the Company which lead to availability of Clinical Supplies and Development Batches to ... and regulatory issues.- Provides technical, project management and system leadership .-Education Minimum Requirement:-BS in Engineering Science, or Information Systems,… more
