Established Products International Physician Fellow

Johnson & Johnson, is recruiting for an Established Products (EP) Physician Fellow to be located in Bogotá, Colombia.

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

The Established Products (EP) International Physician Fellow is an associate member of the EP Clinical and Medical Team assigned to a one-year term (may be extended to include a second year of fellowship) rotating through multiple functional groups within EP within J&J Innovative Medicine.

The goal of the fellowship is to (1) develop leadership, clinical, and medical technical skills in drug development and life-cycle management and (2) gain an understanding of the role of a physician in a pharmaceutical company.

The fellow is assigned to Therapeutic Area Portfolio(s) and supports the Clinical and Compound Development Teams (CDTs) to maximize the value of the portfolio(s). The fellow will be a valuable colleague to work with the extended EP community through rotations with the Clinical, Medical Safety, Medical Affairs and Regulatory Affairs teams.

The fellow will spend up to 60% of their time working with functional coordinators and rotation mentors during each of their 12-18-weeks functional rotations (except Regulatory rotation which will be a floating rotation during the year). In parallel, the fellow will divide the remaining time working with LATAM regional EP MAF team on key assigned projects/activities (20%), engaging in clinical work (10%), engaging in activities led by EP Talent Development Team (5%), and establishing connectivity and network-building opportunities with JNJ stakeholders (5%).

The fellow will have the opportunity to travel to our Titusville site (NJ, United States) two to three times during the program, with each trip lasting approximately two weeks. These visits will include one-on-one meetings with senior leadership, hands-on learning experiences, and participation in key meetings, providing an enriching cross-cultural exchange and fostering global medical insights.

Roles and responsibilities:

- Achieve an overall understanding of how EP is structured/works and how it fits into the overall JNJ Innovative Medicine/OCMO organization.
- Complete the required compliance functional trainings as appropriate for an interim member of the EP Clinical & Medical Team.
- Ensure a clear understanding of the overall goals and objectives of EP’s organization.
- Clinical:

- Contribute to the execution of projects across different phases of clinical development.
- Provide active medical and scientific contribution to cross-functional clinical teams.
- Support successful completion of clinical projects and deliverables that enable worldwide registrations for new indications.
- Complete enhancements to the label and compliance with regulatory commitments for products in the market and in development.
- Support innovative development projects to further enhance the value of our products and the EP organization to JNJ and the patients we serve. Work with the Clinical, Medical Affairs and Medical Safety Leaders, project management leads and extended CDT and their internal/ external partners in the execution of specific tasks and projects related to clinical studies and other tactical strategic activities conducted for the support of the assigned portfolio.
- Work in concert with the Clinical Leaders on clinical trial concept and protocol development, execute clinical studies for new formulations, post-approval commitments, and new indications.
- Be actively involved in creation of Clinical Study Reports, publication of clinical research findings and presentations to relevant FDA, EMA, or other Health Authorities, advisory committees, and review meetings.
- Work with Medical Safety, Medical Affairs, Regulatory Affairs rotation coordinators and their functional teams to learn and get experience in multiple sub-functional areas of responsibility to broaden the fellow’s understanding of the role of a physician in the pharmaceutical industry in a late lifecycle stage of the portfolio of products.
- Participate in cross-functional teams for evaluation of new product ideas and related innovative technologies; review medical literature, medical and market access plans.
- Medical Safety - Participate and complete training