- Bausch Health (Bridgewater, NJ)
- …your skills and values drive our collective progress and impact. The Senior Specialist Regulatory Affairs executes on the pharmaceutical regulatory ... Authorities for assigned brand products + Liaise with country-specific regulatory affairs personnel for international submissions and registrations +… more
- Bausch + Lomb (Trenton, NJ)
- …degree, Bachelor degree preferred or equivalent related training. 0-1 year of Regulatory Affairs experience or related experience in a regulated environment. ... reporting, administrative documentation, due diligence, market expansion, labeling content, regulatory compliance, regulatory intelligence and change management.… more
- AbbVie (Florham Park, NJ)
- …be based on qualifications listed below. Purpose: The Senior Director provides specialist medical and scientific strategic and operational input into core medical ... affairs activities such as: healthcare professional/provider interactions (Payers, Patients,...into and influences the development of asset strategy. Provides specialist medical insights, and executes on data generation, communication,… more
- AbbVie (Florham Park, NJ)
- …will be based on qualifications listed below. Purpose: The Director provides specialist medical and scientific strategic and operational input into core medical ... affairs activities such as: health-care professional and provider interactions;...content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. + Has overall responsibility for… more
- RWJBarnabas Health (Elizabeth, NJ)
- …credentialing information to relevant committees, while acting as a liaison with regulatory agencies and health plans to maintain accurate provider information and ... of the medical staff organization. Preferred: + Certified Provider Credentialing Specialist (CPCS) and /or Certified Professional in Medical Services (CPMSM).… more
- Cardinal Health (Trenton, NJ)
- **What Regulatory Submissions Operations contributes to Cardinal Health** Regulatory provides regulatory affairs and product development consulting ... services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. This function applies subject matter expertise to provide… more
- Stryker (Mahwah, NJ)
- …preferably with medical devices. + A minimum of 2 years in a Regulatory Affairs role required. + Experience in scientific writing, performing systematic ... States. In your role as a Staff Clinical Evaluation Specialist on the Clinical Affairs team, you...data, interpret trends, and communicate scientific findings to support regulatory body submissions for diverse geographies. You will apply… more
- Bayer (Whippany, NJ)
- …biology, chemistry, or related sciences preferred with 10+ years in biomarker/IVD/ regulatory affairs / drug-related development / medical research activities or ... Leaders and the respective late development roles; + Provide specialist IVD/CDx input and reports to early and late...MS degree with 13+ years of biomarker/IVD / regulatory affairs / drug- related development /… more
- Merck (Rahway, NJ)
- **Job Description** **Role Summary** + The Senior Specialist , Global Professional Engagement is a member of the GEMS Consulting & Medical Education team within, V&I ... exists within the broader V&I Global Medical & Scientific Affairs (GMSA), which is part of Our Company Research...of Our Company Research Laboratories (RL). + The Senior Specialist , Global Professional Engagement serves as a key professional… more
- Fujifilm (Trenton, NJ)
- **Position Overview** The Sales Specialist , Diagnostic Oncology, in the Invitro Diagnostics Division, is responsible for identifying, prioritizing, and establishing ... expense tracking and reporting (Salesforce.com) + Where appropriate, collaborate with the Medical Affairs Team. + Follow up to define pathway and respond to customer… more
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