- Merck & Co. (Upper Gwynedd, PA)
- …Management, Regulatory CMC, Regulatory Strategy Development, Regulatory Submissions, Technical Writing -Preferred Skills:Job Posting End Date:08/2/2025 *A ... Scientist, CMC, R4 - Pharm Pre-approval Reporting to the Sr Director / Director /Principal Scientist/Sr Principal Scientist in Pre-approval Pharmaceutical CMC is… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …strong technical knowledge based upon academic training and job experience.Strong oral and writing skill. Able to write regulatory documents in highly complex ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Merck & Co. (Rahway, NJ)
- … Regulatory , Operations, Non-clinical, Clinical, and other functional areasExperience with regulatory submissions including writing / review of regulatory ... robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our Company's success is backed by ethical integrity, forward… more
- Merck & Co. (Rahway, NJ)
- …Infectious Disease, MATLAB, NONMEM, Phoenix WinNonlin, Python (Programming Language), Regulatory Writing , R Programming, Vaccine DevelopmentJob Posting End ... West Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our robust infectious disease and vaccines pipeline. - As an… 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 significant ... cross-functional teams to foster collaboration and innovation.Document Excellence: Author regulatory and technical documentation, ensuring all processes align with… more
- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you. Associate Director , Medical Education - Oncology, is responsible for the strategic planning and ... & Business Agility, Healthcare Environment Dynamics, Inquiry Resolution, Literature Evaluation, Medical Information Writing Skills, Medical Review,… more
- Merck & Co. (North Wales, PA)
- …engagements. This includes the ability to:--Strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) Proven ability to manage competing ... solving, prioritization, conflict resolution, and critical thinking skillsStrong communication, writing , and presentation skillsProficient knowledge in Microsoft office or… more
- City of Spring Hill Kansas (Spring Hill, KS)
- …at the discretion of management, formally or informally, either verbally or in writing . Application Process: 100% City paid medical , dental and vision premiums ... If so, apply now We offer excellent comprehensive benefits including 100% City paid medical , dental and vision premiums for the 2025-2026 Plan Year. We also offer… more
- Eisai, Inc (Nutley, NJ)
- At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... a difference. If this is your profile, we want to hear from you. Director , Clinical Quality Assurance The Director , Clinical Quality Assurance position is… more
- Merck & Co. (North Wales, PA)
- …Ethical Standards, ICH GCP Guidelines, Life Science, Medical Writing , Motivation Management, Ophthalmology, Prioritization, Regulatory Compliance, ... medical protocol deviations in collaborations with the Clinical Director .Other responsibilities include:Collaborating cross-functionally in the development of Protocol… more
- Merck & Co. (Rahway, NJ)
- …Ethical Standards, ICH GCP Guidelines, Life Science, Medical Writing , Motivation Management, Prioritization, Problem Solving, Regulatory Compliance, ... medical protocol deviations in collaborations with the Clinical Director . Other responsibilities include: Collaborating cross-functionally in the development of… more
- Merck & Co. (Rahway, NJ)
- …to high-volume clinical and commercial assembly equipment and processes for medical devices/drug delivery systems. Reporting to the Director responsible ... for this area, you will partake in medical device assembly and process development using semi-automated and automated equipment, conduct functional testing, assist… more
- City of Harrisburg (Harrisburg, PA)
- The City of Harrisburg is accepting applications for the position of Project Director - Asset Management in the Department of Building and Housing Development. The ... Project Director plans, directs, and controls all fiscal activities necessary...(vacation, sick and personal time) and health care benefits ( medical , dental, prescription and vision). The City intends to… more
- Teton Valley Health (Driggs, ID)
- …regulations and other regulatory requirements, such as, DNV, OSHA, etc. The Director , as a Registered Nurse, practices in a surgical services specialty unit by ... Description The Director of Surgical Services is an administrative leader...to communicate effectively in English, both verbally and in writing Basic knowledge in computer use; including email and… more
- Abbott (Alameda, CA)
- …for diversity, working mothers, female executives, and scientists. The Opportunity This Associate Director Regulatory Affairs - APAC will work on-site at our ... Division. As a manager, the function of an Associate Director Regulatory Affairs, APAC (Asia Pacific) is...technical area or MBA Minimum 5+ years' experience in regulatory affairs. Experience working with Medical Devices,… more
- Sutro Biopharma (South San Francisco, CA)
- Description Sutro Biopharma, Inc. is looking for a Director , Regulatory Affairs Medical Writer who will provide leadership in development and execution of ... regulatory authorities. Provide guidance for document development for regulatory writing deliverables, including organization, content, and resource… more
- Scholar Rock (Cambridge, MA)
- …ScholarRock.com and follow @ScholarRock and on LinkedIn. Summary of Position: The Sr. Medical Director , Drug Safety & Pharmacovigilance is a key position within ... expertise, and guidance, pre- and post-approval for assigned products, the Sr. Medical Director will drive the proactive implementation of risk management… more
- Healogics (Melrose Park, IL)
- …care providers across the wound care continuum, Wound Care Center (WCC)(R) Providers, and Medical Director regarding clinic and patient needs. May function as a ... that would benefit through our out-patient clinic partnerships The Clinical Program Director is responsible for the management and the strategic growth of the… more
- MEITHEAL PHARMACEUTICALS INC (Chicago, IL)
- …toward a common goal, for the greater good. Position Summary: The Director of Scientific Communications & Medical Information at Meitheal Pharmaceuticals ... including GPP (Good Publication Practice) and ICMJE standards. Collaborate with clinical, regulatory , and medical affairs team members to ensure publications… more
- LanceSoft (Cambridge, MA)
- Job Title: Director , Signal Management Location: Cambridge, MA 02139 - Remote Duration: 07 Months Objective : Ensures signal detection, evaluation and management ... and leading the development of required processes (eg, with Global Regulatory Affairs, Data Sciences). Ensures that Client Signal Management processes and… more
