Project Responsible Physician

**Position Overview**:
As a Project Responsible Physician (PRP), you will play a vital role in the development and execution of medical strategies and the implementation of a complex compound program, with a primary focus on Alzheimer’s disease. Your contributions will be crucial to the success of our clinical trials, ensuring they meet the highest standards of medical and scientific integrity.

**Key Responsibilities**:
As a Project Responsible Physician (PRP), you will own the development and execution of clinical trial protocols, ensuring they align with strategic goals and are executed to the highest standards in collaboration with Clinical Scientists, Clinical Operations, Medical Monitors, Statistics, and Data Management teams. You will coordinate medical monitoring efforts, evaluate adverse events, and interpret and report research results, preparing them for submission to health authorities. In this role, you will serve as a key medical contact for health authorities, provide consultation to internal partners, and work closely with the Regulatory Affairs team to ensure compliance and address clinical inquiries. Additionally, you will build and present content for Independent Data Monitoring Committee (IDMC) and adjudication meetings, and contribute to the development of presentations and publications of study results.

**Additional Responsibilities**:

- Assist Regulatory Affairs in developing drug regulatory strategies.
- Provide medical-related consultation to ensure unbiased data interpretation.
- Explore and evaluate new assets and products, reviewing medical literature on new technologies.
- Participate in AdBoards & KOL interactions under senior clinical personnel supervision.
- Review clinical trial advertising and promotional materials.

**Principal Relationships**:

- Internal Contacts: Collaborate with Clinical and Compound Development Teams, business development, strategic marketing, legal, and Global Service Organizations.
- External Contacts: Act as a company spokesperson for clinical research findings, assess external clinical research proposals, and develop credible relationships with scientific leaders and regulatory officials.

**Supervision**:
Report to the Clinical Leader or other appropriate supervisors.

**Qualifications**:
**Qualifications**:

- Education: MD (or equivalent) with relevant post-doctoral training and certification; specialist qualification in neuroscience is highly desired.
- Experience: Minimum of 5 years conducting clinical trials in pharma/biotech/CRO or academia.
- Skills:

- Proficiency in written and spoken English.
- Knowledge of Good Clinical Practices and regulatory requirements.
- Strong analytical, decision-making, and critical thinking skills.
- Effective communication and presentation skills.
- Ability to navigate complex relationships and resolve conflicts.
- Proficiency in Microsoft Excel and Word.

Why Join Us?

This is an exciting opportunity to work on innovative healthcare solutions at Johnson & Johnson. You’ll be part of a dynamic, international team, contributing to projects that have a profound impact on global health. We offer a collaborative environment with ample opportunities for personal and professional growth.

We are an equal opportunity employer and value diversity at our company.