Oncology Regulatory Affairs Associate Director

4 weeks ago


Little Rock, United States Sumitomo Pharma Full time

A leading pharmaceutical company is seeking an experienced Associate Director of Regulatory Affairs based in Little Rock, Arkansas. This role involves managing regional regulatory activities and ensuring compliance for oncology products. The ideal candidate will have at least 7 years of experience in the biopharmaceutical industry, with a strong background in regulatory affairs and oncology product development. Competitive salary and comprehensive benefits included.
#J-18808-Ljbffr



  • Little Rock, AR, United States Sumitomo Pharma Full time

    Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets,...


  • Little Rock, United States Arkansas Staffing Full time

    Associate Director Regulatory AffairsSumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early-...


  • Little Rock, United States KMR Search Group Full time

    Sr. Director Regulatory AffairsThis is a remote position.The company is working on a drug/device combination product, they have a lot of expertise on the medical device side, the need the pharmaceutical expertise.This is a new position, the Director has no reports at this time, this person will be able to build their own team over time. The individual will...


  • Little Rock, United States Merck Full time

    A leading pharmaceutical company is seeking a Medical Affairs Director - Health Systems Oncology to develop professional relationships with healthcare decision makers. This role requires an MD, PharmD, or PhD and extensive experience in medical affairs or clinical settings. The director will execute strategic plans, ensuring access to medical information in...


  • Little Rock, United States Arkansas Staffing Full time

    US Director Of Medical AffairsThe US Director of Medical Affairs for Gynecologic Malignancies (Ovarian, Endometrial and Cervical Cancer) holds primary responsibility for the development and execution of regional oncology Medical Affairs strategies and plans for Gynecological Malignancies in the US across indications. The US DMA for Gynecological Malignancies...


  • Little Rock, AR, United States McKesson Full time

    McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve - we care. What you do at McKesson matters. We foster a...


  • Little Rock, United States Arkansas Staffing Full time

    Integration LiaisonBausch + Lomb is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully...


  • Little Rock, United States Sumitomo Pharma Full time

    A global pharmaceutical company is looking for an experienced Associate Director of Regulatory Affairs based in Little Rock, Arkansas. This role requires strong leadership in regulatory strategies, a minimum of 7 years in biopharmaceutical or pharmaceutical industry experience, and excellent communication skills. The position offers a competitive salary of...


  • Little Rock, United States Arkansas Staffing Full time

    Senior/Consultant, Regulatory LabelingIncredible, high-impact role with a Global Biopharma sponsor! Are you ready to turn your labeling expertise into strategic impact? We're seeking a sharp, detail-driven Senior/Consultant, Regulatory Labeling to join a dedicated partnership with a leading global biopharmaceutical company. In this high-visibility role,...


  • Little Rock, United States Arkansas Staffing Full time

    Cmc Regulatory Affairs Senior/ConsultantExciting opportunity for an experienced and highly motivated professional to join our global regulatory affairs team. This role is critical to ensure our client's investigational, new, and marketed small molecule products are developed and maintained in compliance with global regulatory requirements. The primary...