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Senior Director, Clinical Lead – Neuropsychiatry
Johnson & JohnsonSenior 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
✓ 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 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