- J&J Family of Companies (Raleigh, NC)
- Director , Regulatory Medical Writing (1 of 4) - 2406211847W **Description** Johnson & Johnson is currently seeking a Director , Regulatory ... people can reach their potential. At Johnson & Johnson, we all belong. The Director , Regulatory Medical Writing (RegMW) is a highly experienced … more
- Takeda Pharmaceuticals (Raleigh, NC)
- … response documents and key components of regulatory submissions. + The Associate Director , Medical Writing is seen as an expert in medical ... therapies to patients worldwide. Join Takeda as a Associate Director Medical Writing where you...documents. Collaborate with all Takeda regions to ensure a medical writing regulatory document strategy… more
- Takeda Pharmaceuticals (Raleigh, NC)
- …the best of my knowledge. **Job Description** **About the role:** **Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology ... contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing...US based employees may be eligible to participate in medical , dental, vision insurance, a 401(k) plan and company… more
- J&J Family of Companies (Raleigh, NC)
- Associate Director , CMC Regulatory Affairs - 2406221330W **Description** Johnson & Johnson is recruiting for an Associate Director , CMC Regulatory ... Authorities. + Provides technical expertise and technical input in the preparation and writing (as applicable) of regulatory dossiers for submission to Health… more
- Organon & Co. (Raleigh, NC)
- …support the approved early development plans. The TMED Lead will serve as the medical monitor and/or study director responsible for the execution (in conjunction ... **The** **Position** **This position can be 100% remote in the US** The Director , Translational Medicine and Early Development (TMED) Lead will be responsible for… more
- Cardinal Health (Raleigh, NC)
- …(CMC) Development + Nonclinical Development and Consulting + Clinical Development and Research + Medical Writing + Regulatory Publishing + Dossier Services + ... & Filing + Quality Review Standards + Drug, Biologic (IV, Injectable) and Medical Device Development + Regulatory Outsourcing + Pharmaceutical Compliance + … more
- ThermoFisher Scientific (Morrisville, NC)
- …Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Overview:** Provides medical oversight of clinical trials to ensure company SOPs, client ... directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides medical … more
- Fujifilm (Raleigh, NC)
- **Overview** As the Associate Director of Biosafety, you will serve as the Corporate Biosafety Officer (BSO) and provide expertise in biorisk management, ... and safety. This position will report to the Global Director , Biosafety and Toxicology, and sit under the global...Toxicology, and sit under the global quality leadership group ( Regulatory , IT, Safety, QA, and QC). **External US** The… more
- J&J Family of Companies (Raleigh, NC)
- Program Director - PSC - 00001LCI **Description** Johnson & Johnson is currently seeking a Program Director to join our Patient Service Center Team. While this ... Johnson & Johnson, we all belong. Purpose: The Program Director will be solely dedicated to the management of...facing role. + Working Knowledge of Reimbursement Pharmacy and/or Medical benefits + Prior experience and knowledge with pharmacy… more
- Merck (Wilson, NC)
- …standards while minimizing environmental waste and impact. **Job Description** This Associate Director , MDCP Operations Lead position will serve as the primary ... medical device and combination product (MDCP) point of contact...that are both compliant and pragmatic. **Responsibilities** The Associate Director , MDCP Operations Lead position is responsible for providing… more
- West Pharmaceutical Services (Raleigh, NC)
- …with a good technical understanding and knowledge of combination products, medical device qualification, primary packaging, regulatory requirements, and program ... Director , Business Development for Drug Packaging and Delivery...candidate will have a strong background in pharmaceuticals and medical device, with a deep understanding of drug delivery… more
- Takeda Pharmaceuticals (Raleigh, NC)
- …writing strategy for key clinical and regulatory documents and regulatory submissions; guides medical writing document preparation, including ... Writing team, you will report to the Associate Director . **How you will contribute:** + Reporting to a...Principal Medical Writer guides medical writing activities for key clinical and regulatory … more
- Perdue Farms, Inc. (Raleigh, NC)
- …safety program throughout live production in conjunction with the collocated safety director . + Partner with the Perdue Agribusiness safety teams at cohabitated feed ... mill sites to ensure compliance with regulatory requirements and corporate standards. + Directly leads & manages, safety for live production operations… more
- CVS Health (Raleigh, NC)
- …activities (vaccine clinics, inventories, remodels, pilots, rollouts, etc.), compliant with regulatory guidelines, and embracing change and new ways of working. The ... Review communications from CSC (Weekly myWork Communication) and Region Director to brief DL, RX on key priorities and.... Strong communication skills in both formal and informal writing and speech . Proven ability to work with… more
- RELX INC (Raleigh, NC)
- …and analytical Marketing Analyst to join our Marketing team. Reporting to the Sr. Director of Demand & Marketing Operations, you will play a key role in collecting, ... experience + 5+ years of experience in analytics + Exceptional communication, writing , and organizational skills + Well-organized with high attention to detail +… more