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Johnson & Johnson

Senior Director, Clinical Lead – Neuropsychiatry

Johnson & Johnson

Senior Director, Clinical Lead at Johnson & Johnson overseeing medical strategies for late phase compounds. Leading cross-functional teams to develop products efficiently and effectively.

Posted 5/7/2026full-timeTitusville • Massachusetts, New Jersey, Pennsylvania • 🇺🇸 United StatesSenior💰 $226,000 - $391,000 per yearWebsite

About the role

Key responsibilities & impact
  • Responsible for the development and execution of the clinical development plan
  • Leads Cross-functional Clinical Team; supervises, develops and recruits junior medical staff
  • Molecule responsible physician
  • Responsible for the oversite of medical monitoring/reporting and safety activities
  • Evaluates adverse events (pre and post-marketing) for relationship to treatment
  • Responsible for overseeing content for the Independent Data Monitoring Committee (IDMC) and adjudication meetings as needed
  • Interprets, reports and prepares results of product research in preparation for global health authority submissions and external communication
  • Responsible for assessment of medical publications emerging from the Team and its affiliates
  • Assists Regulatory Affairs in the development of drug/device regulatory strategies
  • Acts as medical contact at company for global health authorities concerning clinical/medical issues
  • May act as company spokesperson regarding publication of clinical research findings and presentations to relevant global health authorities and advisory committees
  • Helps explore and evaluate new product ideas to assist in identifying new marketing opportunities
  • Supports general Clinical/Medical Affairs activities involving product evaluation, labeling and surveillance
  • Supports early clinical development involving product potential and development for registration
  • Manages the budget for all project related clinical activities

Requirements

What you’ll need
  • MD (or equivalent) in relevant area with appropriate post-doctoral training and certification
  • A minimum of 5 years clinical research or pharmaceutical industry experience
  • A minimum of 3 years of Phase II/III development experience within industry
  • Board Certification or Eligibility in Psychiatry or neurology preferred
  • A minimum of 3 years of highly successful managerial/supervisory or related experience
  • Expertise in clinical drug development including demonstrated ability to develop clinical development plans meeting the highest standards
  • Global registration experience strongly preferred
  • Experience working in a Matrix environment is required
  • Ability to interface effectively with clinical operations, medical affairs and marketing is essential
  • Fluent in written and spoken English
  • Working knowledge of the use of Microsoft suite of software products including Excel and Word
  • Experience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filings

Benefits

Comp & perks
  • medical
  • dental
  • vision
  • life insurance
  • short- and long-term disability
  • business accident insurance
  • group legal insurance
  • retirement plan (pension)
  • savings plan (401(k))
  • long-term incentive program
  • vacation – 120 hours per calendar year
  • sick time - 40 hours per calendar year; for employees who reside in the State of Washington – 56 hours per calendar year
  • holiday pay, including Floating Holidays – 13 days per calendar year
  • Work, Personal and Family Time - up to 40 hours per calendar year
  • Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
  • Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member
  • Caregiver Leave – 10 days
  • Volunteer Leave – 4 days
  • Military Spouse Time-Off – 80 hours

ATS Keywords

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Hard Skills & Tools
clinical development planclinical researchPhase II developmentPhase III developmentclinical drug developmentmedical monitoringadverse event evaluationregulatory strategiesclinical trial conductregulatory filings
Soft Skills
leadershipsupervisory experienceinterpersonal skillscommunication skillsmanagerial experienceteam developmentbudget managementcross-functional collaborationproblem-solvingstrategic thinking
Certifications
MDBoard Certification in PsychiatryBoard Certification in Neurologypost-doctoral trainingclinical research certification