Study Responsible Physician- Neuroscience Late Development

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Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

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Discovery & Pre-Clinical/Clinical Development

Clinical Development & Research – MD

People Leader

Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America

Johnson & Johnson, is recruiting for a Neuroscience Late Development Study Responsible Physician (SRP) to be based at one of our sites in Titusville, NJ or Spring House, PA. Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Our Neuroscience team tackles the world’s toughest brain health challenges including multiple sclerosis, Alzheimer’s disease, Parkinson’s disease, myasthenia gravis, epilepsy, major depressive disorder, bipolar disorder, schizophrenia, and autism. This patient-focused team helps address some of the most complex diseases of our time. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

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Responsible for medical monitoring/reporting and company safety officer activities

Works on clinical development plans, trial protocols and takes ownership of clinical study reports

Evaluates adverse events (pre- and post-marketing) for relationship to treatment

Assists Regulatory Affairs in determining requirements for any corrective actions or health authority reporting related to study conduct or outcome

May act as a medical contact at the company for health authorities concerning clinical/medical issues

Interprets, reports, and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissions

Close interactions with Project Clinical Scientists and Physicians across programs

Assists Regulatory Affairs in the development of drug regulatory strategies

Executes medical-related consultation for internal stakeholders to ensure unbiased data interpretation

May help explore and evaluate new assets (BD) and/or products to support compound value, including review of medical literature related new technologies

Participates in AdBoards & KOL interactions where required (together with / under supervisor of senior clinical personnel)

Participates in the development of presentations and publications of study results

MD (or equivalent) in relevant area; MD/PhD.

Experience in neuroscience (psychiatry, neurology) highly preferred.

Minimum of 1 year conducting clinical trials in pharma/biotech/CRO or minimum of 2 years conducting clinical trials in academia.

Experience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filings.

Solid analytical and critical thinking skills, with the ability to interpret and leverage data for decision making.

Strong communication and presentation skills to effectively convey complex ideas and strategic insights to stakeholders.

Independent decision making and analytical skills are required.

Ability to navigate complex relationships and resolve conflicts effectively.

Exceptional interpersonal and communication skills, with the ability to build…