Assistant Medical Director (Psychiatrist) | Middletown, CT | Direct Hire The Provider FinderAssistant Medical Director (Psychiatrist) | Middletown, CT | Direct HireMiddletown, New JerseyIncumbents in this class must possess and retain certification as a specialist in psychiatry by the American Board of Psychiatry and Neurology OR certification in the field of internal medicine, family medicine or related specialty, from an appropriate specialist board. In the Department of Mental Health and Addiction Services this class is accountable for assisting in administering agency medical, clinical and behavioral health services programs and operations within a hospital division.
Statewide Associate Medical Director UCHC Administration Rutgers The State University of New JerseyStatewide Associate Medical Director UCHC AdministrationNew Brunswick, NJUnder Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption. University Correctional Health Care (UCHC), operating within Rutgers, The State University of New Jersey, is dedicated to excellence in providing physical, mental health, dental and sex offender treatment services to those involved in the criminal justice systems in New Jersey.
Psychiatrist :-Medical Director | Middletown, CT | Direct Hire The Provider FinderPsychiatrist :-Medical Director | Middletown, CT | Direct HireMiddletown, New Jerseycare programs, services and operations; Participates on various committees and boards; Leads the recruitment and hiring of staff, including outreach, interview and selection; May testify in court as needed; May conduct training; May be responsible for coordination of accreditation activities; May serve as agency liaison with external medical, behavioral health planning, advisory. groups, courts and other state medical and service agencies; May monitor contracts with medical services vendors; May participate in quality assurance studies and investigations; May develop processes and practices to improve quality and cost of patient care; Performs related duties as required.
Senior Account Director Business Development (Medical Communications) -US -Remote Thermo Fisher Scientific IncSenior Account Director Business Development (Medical Communications) -US -RemoteNJRemote$108,000–$180,000 / yearSummarized Purpose: The Senior Account Director Business Development secures and retains business for PPD through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need.
Associate Director, Project Management - Medical Affairs (Princeton, NJ or Palo Alto, CA) Summit TherapeuticsAssociate Director, Project Management - Medical Affairs (Princeton, NJ or Palo Alto, CA)Princeton, New Jersey$175,000–$200,000 / yearHARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. The role will serve as a central point of contact for operational planning, delivery, and governance of critical Medical Affairs projects—spanning scientific communications, congress strategy, advisory boards, medical education, and post-marketing data generation supporting launch preparation.
Senior Director, North America Field Medical Affairs - Endocrinology Recordati SpASenior Director, North America Field Medical Affairs - EndocrinologyBridgewater, NJRecordati Rare Diseases, Inc. (RRD) develops high-impact therapies for devastating rare diseases, focusing on providing often overlooked treatments to underserved communities in the U.S. Our mission is to mitigate the impact of rare diseases through increased awareness, improved diagnoses, and enhanced treatment availability, covering endocrinology, metabolic, and oncology franchises. Provides coordination and facilitation of MSL field research activities including assessment and selection of clinical investigators, site identification in relation to RRD clinical trials on marketed products, product line extensions, and products under development; as well as investigator sponsored studies.
Associate Director, Project Management - Medical Affairs Princeton, NJ or Palo Alto, CA Summit Therapeutics IncAssociate Director, Project Management - Medical Affairs Princeton, NJ or Palo Alto, CAPrinceton, NJ$175,000–$200,000 / yearHARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. The role will serve as a central point of contact for operational planning, delivery, and governance of critical Medical Affairs projects-spanning scientific communications, congress strategy, advisory boards, medical education, and post-marketing data generation supporting launch preparation.
Director, Global Medical Affairs, US Rheumatology Bristol Myers SquibbDirector, Global Medical Affairs, US RheumatologyPrinceton, NJ$207,490–$251,433 / 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.
Director, Medical Safety Assessment Physician, Neuroscience Bristol Myers SquibbDirector, Medical Safety Assessment Physician, NeurosciencePrinceton, 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.
Director, Medical Safety Assessment Physician Bristol-Myers Squibb CoDirector, Medical Safety Assessment PhysicianPrinceton Pike, 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.
Sr Scientific Advisor, Medical Communications IQVIA Holdings IncSr Scientific Advisor, Medical CommunicationsParsippany, NJ$99,300–$248,300 / yearProactively partners with internal and external partners to develop and implement a compliant strategy and framework for the delivery and communication of key scientific, pipeline, or clinical insights in line with client objectives. Ability to travel for representation of company at client meetings, advisory boards, medical or industry conferences, pitch presentations, and other meetings as needed.
Executive Director, Real World Evidence Innovation Center Lead, Global Medical Bristol Myers SquibbExecutive Director, Real World Evidence Innovation Center Lead, Global MedicalPrinceton, NJ$254,530–$308,434 / yearA core priority is working with the Data Analytics and HEOR teams to identifying and integrating the growing portfolio of available therapeutic area-level data sources - including EMR/EHR, claims, registries, specialty datasets, and partner platforms - and making those assets practically accessible and scientifically deployable for the MEG, MAP & RWE and Global Medical teams. Design and deliver an enterprise RWD training curriculum - covering database literacy, advanced study designs (ECAs, hybrid, RWD-supplemented trials), AI/digital approaches, and data acquisition pathways - targeted at MEG & MAP study teams.
Director, Regional Medical Market Lead, INTERCON (Pumitamig) Bristol Myers SquibbDirector, Regional Medical Market Lead, INTERCON (Pumitamig)Princeton, NJ$207,490–$251,433 / yearLead visibility and prioritization of market level evidence gaps as a key driver of Evidence Generation, guiding markets through NIR and IEP related processes, informing Integrated Evidence Plans (IEP), and steering regional discussions to ensure local evidence needs are fully reflected in medical plans. 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 Medical Excellence & Training Director (Remote - East Coast) United Therapeutics CorpAssociate Medical Excellence & Training Director (Remote - East Coast)New Jersey, NJRemote$182,500–$240,000 / yearThe Associate Medical Excellence & Training Director will work closely with senior management, Clinical Practice Liaisons (CPLs), MSL Field Directors, MSLs and internal Medical Affairs counterparts and other cross functional partners and will be responsible for planning, designing, implementing, and evaluating training programs for new hires and continuous education of MSLs and other GMA colleagues. Doctor of Pharmacy (PharmD) or Doctor of Philosophy (PhD) in clinical areas of interest preferably with 7+ years of experience in Medical Affairs supporting specialty care compound/products or clinical practice in PAH/PH-ILD/ILD patient care, or a combination of both with a PharmD or PhD or.
MSL Lead Novartis AGMSL LeadEast Hanover, NJ$289,500–$537,600 / yearExpected Annual Base Salary Range for role: Poland: PLN 289,500 - 537,600 The salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. This is an opportunity to combine your scientific expertise, leadership capability, and strategic mindset to influence medical decision-making, strengthen external partnerships, generate valuable insights, and advance patient outcomes through credible, evidence-based exchange.
2027 Future Talent Program - Global Scientific Value Content - Intern Merck & Co Inc2027 Future Talent Program - Global Scientific Value Content - InternRahway, NJ$39,908–$111,111 / yearWith guidance from preceptor, candidate will connect with key stakeholders (e.g., Global Medical Information, Global Scientific Training, Scientific Affairs, Publications, Medical Science Liaisons, Compliance, Clinical, Value and Implementation Outcomes Research to learn more about the cross-functional collaboration between functional areas in the pharmaceutical industry. With guidance from the preceptor, a successful candidate will gain experience collaborating with key stakeholders such as Global Medical Affairs experts, Observational and Real-World Evidence researchers, and Medical Science Liaisons.
New[PRI] Director -Analytics ProcDNA[PRI] Director -AnalyticsPrinceton, NJFull timeYou'll operate with real autonomy — shaping solutions to underdefined problems, driving proposals and engagements forward without needing a fully scripted brief — while knowing when to pull in practice leadership for strategic or high-stakes calls rather than working around them. Occasional involvement is expected in specific contexts — for example, supporting primary market research, advisory boards, or similar client-facing research activities — but the role is not built around running field medical or investigator relationships.
Clinical Manager - Full Time Penn MedicineClinical Manager - Full TimePrinceton, NJ$78,265.82–$124,813.73 / yearSummary: Under supervision from the Director of outpatient services and other clinical directors, provides comprehensive oversight of the program including senior level clinical leadership in treatment planning and patient care, program development and refinement, supervision and evaluation of staff performance and performance improvement activities. Regulatory Oversight: Work with administrative director to ensure that the program remains in compliance with various regulatory bodies such as Joint Commission, Medicare, Medicaid, and the New Jersey DHS, DMHAS and DCF.
Senior Manager, CRM IT Summit Therapeutics plcSenior Manager, CRM ITPrinceton, NJOverview of Role: The Senior Manager, CRM IT will serve as the technology and business process leader for Veeva CRM, partnering closely with Commercial Operations, Sales, Medical Affairs, Market Access, and IT leadership to define, implement, optimize, and support CRM capabilities across the organization. The ideal candidate will possess deep expertise in pharmaceutical commercial operations and hands-on experience implementing and managing Veeva CRM solutions supporting Sales, Medical Affairs, Key Account Management, Market Access, and Field Reimbursement teams.
Senior Manager, CRM IT Summit TherapeuticsSenior Manager, CRM ITPrinceton, New JerseyThe Senior Manager, CRM IT will serve as the technology and business process leader for Veeva CRM, partnering closely with Commercial Operations, Sales, Medical Affairs, Market Access, and IT leadership to define, implement, optimize, and support CRM capabilities across the organization. HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.