Adult Congenital Heart Disease (ACHD) Cardiologist – Medical Director RWJBarnabas HealthAdult Congenital Heart Disease (ACHD) Cardiologist – Medical DirectorNewark, NJ$500,000–$700,000 / yearNewark Beth Israel Medical Center (NBI), part of RWJBarnabas Healththe largest academic health system in New Jerseyis seeking an experienced Adult Congenital Heart Disease (ACHD) cardiologist to lead and expand our established ACHD program. This leadership role will guide the program toward ACHA accreditation while integrating multidisciplinary care across cardiology, cardiac surgery, maternal-fetal medicine, electrophysiology, imaging, and advanced heart failure and transplant services.
Join RWJBarnabas Health as Medical Director of Occupational Medicine – (Livingston, NJ) RWJBarnabas HealthJoin RWJBarnabas Health as Medical Director of Occupational Medicine – (Livingston, NJ)Livingston, NJ$240,000–$340,000 / yearRWJBarnabas Health, the largest and most comprehensive integrated healthcare system in New Jersey, is actively seeking an experienced, board-certified Occupational Medicine physician for our Occupational Health and Employee Health Services at Essex County Hub located in Livingston, NJ. We deliver best-in-class occupational medicine services, including injury care, regulatory surveillance, pre-employment physicals, DOT exams, and wellness programs – all grounded in regulatory excellence and patient-centered outcomes.
Associate Director Medical Science Liaison - East IQVIA Holdings IncAssociate Director Medical Science Liaison - EastNew York, NY$230,000–$280,000 / yearEDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience - Requirements: Master's level oncology PA or NP degree with active commitment towards completion of doctorate degree preferred and a minimum of 13 years of related experience; or, Accredited doctorate degree in a basic-science or life-science discipline (Pharm. Direct and indirect responsibilities include solid tumor oncology HCP engagement, investigator-initiated studies, support of company sponsored trials, scientific congress support, development of MSL plans, and management of a regional MSL team as assigned.
Director, Medical Safety Assessment Physician Bristol-Myers Squibb CoDirector, Medical Safety Assessment PhysicianMadison, NJ$286,560–$347,244 / yearOversee, prepare and/or review aggregate safety review documents (eg, Development Safety Update Reports [DSUR], Periodic Benefit-Risk Evaluation Reports [PBRER]) and safety sections of relevant clinical trial documents (eg, protocols, clinical study reports [CSR], investigator brochures [IB], informed consent forms [ICF]) and regulatory filings (eg, clinical trial applications [CTA], marketing authorization applications [MAA]). Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Associate Director, Global Medical Affairs Publication Operations Johnson & JohnsonAssociate Director, Global Medical Affairs Publication OperationsRaritan, NJ$137,000–$235,750 / yearFamiliar with the overall publication plan for product(s) and proactively fulfills Pub Ops' role in generating assigned publications, including assigning medical writers and providing editing and project management to efficiently deliver high-quality publications to author teams. · Please use the following language: • Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Director, Medical Strategy - VP IHH Rise&RunDirector, Medical Strategy - VPNew York, New YorkOmnicom’s policy requires employees to work in the office for a minimum of three days a week, unless additional in-office days are directed by their agency or manager. * Experience developing and delivering strategic medical communications content, including scientific platforms, brand planning documents, and pitches.
Sr Medical Director Clinical Development - Radiopharmaceuticals HCC and GI cancers Bristol-Myers Squibb CoSr Medical Director Clinical Development - Radiopharmaceuticals HCC and GI cancersNY$306,814–$371,787 / yearRayzeBio has assets in development for hepatocellular carcinoma (HCC), both as diagnostic and therapeutic, and the Clinical Development Lead will have responsibility to oversee the clinical development plans for these assets across the full range of the development lifecycle, from IND to Phase 3 registrational studies. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Medical Strategy Director- Advertising Fifth ElementMedical Strategy Director- AdvertisingNew York, NY$145,000–$160,000 / yearYou lead medical strategy across major brands and therapy areas, shaping direction, guiding teams, and building trust with clients at a senior level. Lead complex, high-visibility accounts with strong judgment and steady decision-making.
Rutgers Robert Wood Johnson Medical School is seeking a Gastroenterologist to serve as Clinical Director RWJBarnabas HealthRutgers Robert Wood Johnson Medical School is seeking a Gastroenterologist to serve as Clinical DirectorNew Brunswick, NJRutgers Robert Wood Johnson Medical School is seeking a gastroenterologist to serve as Clinical Director of Gastroenterology and oversee the clinical operations of the Division of Gastroenterology and Hepatology, ensuring high-quality care, operational efficiency, and strategic alignment with the organizations goals. Managing our gastroenterologists clinical performance and activities, overseeing clinical staff, developing and implementing clinical strategies, and improving patient outcomes through collaboration with multidisciplinary.
Medical Scientific Director Teva Pharmaceutical Industries LtdMedical Scientific DirectorParsippany, NJ$212,160–$265,200 / yearAdditional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible, Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. The Medical Scientific Director serves as a scientific and strategic partner within Teva's Medical Affairs organization, supporting both early‑stage and mature assets, including- but not only- respiratory therapies (e.g., ICS/SABA combinations) and neurology products (e.g., AJOVY).
Director, Medical Performance Measurement Bristol-Myers Squibb CoDirector, Medical Performance MeasurementPrinceton Pike, NJ$190,060–$230,308 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Senior Director, Medical Performance Measurement Bristol-Myers Squibb CoSenior Director, Medical Performance MeasurementPrinceton Pike, NJ$224,910–$272,538 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
NewDirector, Vaccines Portfolio Medical Strategy and Communications PfizerDirector, Vaccines Portfolio Medical Strategy and CommunicationsPearl River, Massachusetts$176,600–$294,300 / yearReporting to the Senior Director, Medical Scientific Communications and Content, Vaccines, in this portfolio-wide, cross-pathogen role, you will be responsible for developing and advancing an integrated medical strategy and unified scientific narrative for Pfizer Vaccines, connecting evidence across pathogens and positioning Pfizer as a rigorous scientific reference point in vaccines across all stages of life. Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
Clinical Development Medical Senior Director (MD Required) PfizerClinical Development Medical Senior Director (MD Required)New York City, NY$274,500–$457,500 / yearProvides clinical guidance to the development of the clinical data collection strategy, instruments, and data review plan, ensuring alignment with the protocol and SAP, optimized data collection principles, and clinical data review best practice; sets the clinical data review strategy and leads the team in the review of emerging clinical data and trends; reviews and queries data; presents data to internal and external stakeholders; partners with site-facing colleagues in support of data issue resolution; ensures all clinical queries are appropriately addressed in support of database lock. Provides clinical guidance to the development of the Safety Review Plan and Safety Narrative Plan; reviews safety data and ensures clinical documents are updated in response to emerging safety profile; tracks and reconciles Serious Adverse Events; leads clinical safety data discussion during Safety Review Team meetings in collaboration with Medically Qualified Individual(s); reviews safety narratives.
Senior Director Medical Affairs (COVID-19/Viral Diseases) Shionogi Inc.Senior Director Medical Affairs (COVID-19/Viral Diseases)Florham Park, New Jersey$280,000–$350,000 / yearPartner with the Clinical Research team in the planning and review of Clinical Research programs, protocols and final study reports for clinical development projects, as well as in Clinical Research programs needed for the support of existing products and claims. This Senior Director Medical Affairs will have primary responsibility for the COVID-19/Viral Diseases COVID-19/Viral Diseases disease portfolio, with the flexibility to expand into other product areas as needed and as Shionogi Inc. continues to grow.
Dermatology Residency Program Director – Robert Wood Johnson Medical School RWJBarnabas HealthDermatology Residency Program Director – Robert Wood Johnson Medical SchoolNew Brunswick, NJSubmit accurate and complete information required and requested by the DIO, GMEC, and ACGME; Provide applicants who are offered an interview with information related to the applicants eligibility for the relevant specialty board examination(s); Provide a learning and working environment in which residents have the opportunity to raise concerns and provide feedback in a confidential manner as appropriate, without fear of intimidation or retaliation; ensure the programs compliance with the Sponsoring Institutions policies and procedures related to grievances and due process; Ensure the programs compliance with the Sponsoring Institutions policies and procedures for due process when action is taken to suspend or dismiss, not to promote, or not to renew the appointment of a resident; A program does not operate independently of its Sponsoring Institution. To perform this job successfully, an individual must include specialty expertise must include current certification in the specialty for which they are the program director by the American Board of Dermatology; must include current medical licensure and appropriate medical staff appointment; must include ongoing clinical activity; and, A program director is a role model for faculty members and residents.
Covid-19 Vaccines, Medical Evidence Strategy Lead - MD (Sr. Director) PfizerCovid-19 Vaccines, Medical Evidence Strategy Lead - MD (Sr. Director)Pearl River, NY$254,100–$423,500 / yearThe foremost priority will be in setting strategy for the generation of real-world evidence across Pfizer and in collaboration with BioNTech to ensure COVID-19 studies are conducted with scientific rigor and operational efficiency in support of regulatory requirements, public health needs and education of and interactions with healthcare providers. The individual filling this position will assume the role of the Global Medical Evidence Strategy Lead within the COVID-19 vaccine franchise and will assume primary responsibility for overseeing the strategy for COVID-19 medical evidence generation and interpretation; to include but not limited to vaccine effectiveness and COVID-19/SARS-CoV-2 burden studies.
COVID-19 Vaccines, Medical Evidence Strategy Lead (Sr. Director) PfizerCOVID-19 Vaccines, Medical Evidence Strategy Lead (Sr. Director)Pearl River, Pennsylvania$230,900–$384,800 / yearThe foremost priority will be in setting strategy for the generation of real-world evidence across Pfizer and in collaboration with BioNTech to ensure COVID-19 studies are conducted with scientific rigor and operational efficiency in support of regulatory requirements, public health needs and education of and interactions with healthcare providers. The individual filling this position will assume the role of the Global Medical Evidence Strategy Lead within the COVID-19 vaccine franchise and will assume primary responsibility for overseeing the strategy for COVID-19 medical evidence generation and interpretation; to include but not limited to vaccine effectiveness and COVID-19/SARS-CoV-2 burden studies.
Associate Director Marketing, HCP Medical Education Teva Pharmaceutical Industries LtdAssociate Director Marketing, HCP Medical EducationParsippany, NJ$154,160–$202,335 / yearAdditional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible, Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. Build and execute portfolio-wide plans in conjunction with other marketing disciplines, including KOL Engagement/Congress Planning and Thought Leader Liaison (TLL) teams, including a specific focus on brand-related content for congresses/conventions focused on movement disorders and acting as the liaison to Speakers.
Covid-19 Vaccines, Medical Evidence Strategy Lead (Sr. Director) PfizerCovid-19 Vaccines, Medical Evidence Strategy Lead (Sr. Director)New York City, NY$230,900–$384,800 / yearThe foremost priority will be in setting strategy for the generation of real-world evidence across Pfizer and in collaboration with BioNTech to ensure COVID-19 studies are conducted with scientific rigor and operational efficiency in support of regulatory requirements, public health needs and education of and interactions with healthcare providers. The individual filling this position will assume the role of the Global Medical Evidence Strategy Lead within the COVID-19 vaccine franchise and will assume primary responsibility for overseeing the strategy for COVID-19 medical evidence generation and interpretation; to include but not limited to vaccine effectiveness and COVID-19/SARS-CoV-2 burden studies.