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Johnson & Johnson

Senior Director, Clinical Lead – Neuropsychiatry

Johnson & Johnson

Senior Director, Clinical Leader responsible for late phase compound strategies at Johnson & Johnson. Leading cross-functional teams to develop impactful healthcare solutions.

Posted 6/5/2026full-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 and has ownership for the design of clinical trials and for the content of clinical study reports
  • 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 and determining requirements for any corrective actions or health authority reporting
  • 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 is required, inclusive of 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 is required.
  • Global registration experience strongly preferred, as is experience working or interacting with Health Authorities.
  • 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
  • pension plan
  • 401(k)
  • vacation – 120 hours per calendar year
  • sick time - 40 hours per calendar year
  • holiday pay – 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 trials designmedical monitoringadverse event evaluationregulatory strategiesclinical drug developmentPhase II developmentPhase III developmentGood Clinical Practicesregulatory requirements
Soft Skills
leadershipsupervisory skillsinterpersonal skillscommunication skillsmanagerial experienceteam developmentbudget managementcross-functional collaborationproblem-solvingstrategic thinking
Certifications
MDBoard Certification in PsychiatryBoard Certification in Neurology