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Senior Director, Clinical Lead – Neuropsychiatry
Johnson & JohnsonSenior 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
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
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