1 день назад
Study Responsible Physician - Neuroscience Late Development
199 000 - 343 850$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Study Responsible Physician - Neuroscience Late Development (clinical development and neuroscience): Designing and executing Phase 2/3 neuroscience clinical studies with an accent on medical monitoring, patient safety, regulatory filings, and clinical study reporting. Focus on evaluating adverse events, interpreting clinical data, supporting regulatory strategies, and collaborating across matrixed clinical and scientific teams.
Location: Titusville, New Jersey; Cambridge, Massachusetts; or Spring House, Pennsylvania, United States. The role is associated with multiple country postings in the United States, Belgium, and Switzerland. Hybrid work is indicated.
Salary: $199,000–$343,850 per year.
Company
Johnson & Johnson develops healthcare and medical solutions, including medicines and MedTech products, across complex diseases and patient-care needs.
What you will do
- Design and execute Phase 2/3 clinical studies within the Neuroscience Late Development portfolio.
- Contribute to clinical development plans, trial protocols, protocol training materials, clinical study reports, and regulatory documents.
- Provide medical monitoring and safety oversight through data reviews, adverse-event evaluation, medical-history coding, protocol-deviation review, and site interactions.
- Support health-authority communications, corrective-action decisions, regulatory strategies, and drug-safety reporting.
- Interpret research results and prepare presentations and publications with senior clinical personnel.
- Collaborate with clinical operations, project management, regulatory affairs, data management, biostatistics, medical writing, legal, quality, and safety functions.
Requirements
- MD or equivalent degree in a relevant area; MD/PhD is applicable.
- At least 1 year of clinical-trial experience in pharma, biotech, or a CRO, or at least 2 years in academia.
- Knowledge of Good Clinical Practices and regulatory requirements for clinical trials and regulatory filings.
- Fluent written and spoken English required.
- Analytical, critical-thinking, communication, presentation, problem-solving, and conflict-resolution skills.
- Experience leading and managing work in a matrix organization, including influencing without direct reporting authority.
Nice to have
- Experience in neuroscience, psychiatry, or neurology.
- MD/PhD qualification.
- Experience evaluating scientific opportunities, new assets, or products in the therapeutic area.
Culture & Benefits
- Patient-focused work addressing neurological and psychiatric conditions including multiple sclerosis, Alzheimer’s disease, Parkinson’s disease, epilepsy, and schizophrenia.
- Retirement pension and 401(k) savings plans.
- Eligibility for a long-term incentive program.
- Vacation, sick time, holidays, parental leave, caregiver leave, bereavement leave, volunteer leave, and military spouse time-off benefits.
- Inclusive workplace and interview accommodations for applicants with disabilities.
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