Johnson & Johnson companies are equal opportunity employers.
Senior Director, Woman's Health, Established Products Portfolio, Compound Development Team Leader-00000QGT
Description
Janssen Pharmaceutical Research & Development, L.L.C., a member of the Johnson & Johnson Family of Companies, is recruiting for a Senior Director, Womens Health, Established Products Portfolio/Compound Development Team Leader. This position will be based in Titusville NJ, Raritan NJ, High Wycombe UK, Beerse Belgium, or Singapore Singapore.
Janssen Research & Development, L.L.C. develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, and reproductive medicine.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
The Portfolio/Compound Development Team Leader (P/CDTL) is responsible for development and execution of the portfolio and compound strategies for multiple marketed products. The P/CDTL will directly supervise at least one Clinical Leader assigned to support the portfolio. Operational implementation is delivered through effective leadership of many cross-functional Compound Development Teams and the Portfolio, often including support for global registration and marketing efforts. The P/CDTL leads the team to support and develop products in a timely and cost effective manner, and is responsible for the execution of multiple compound strategies. Team leadership via matrix interactions includes individuals from line functions such as Clinical, Project Management, Global Regulatory Affairs, Pharmaceutical Development & Manufacturing Sciences (PDMS), Clinical Pharmacology, Global Strategic Marketing, Global Medical Safety, Janssen Supply Chain (JSC) , Drug Safety Sciences and other scientific and business related disciplines.
The Portfolio/Compound Development Team Leader (P/CDTL) actively contributes to Compound Strategy decisions of multiple CDTs by providing relevant strategic perspective, expertise and senior level guidance. S/he will lead the development and maintenance of the multiple integrated project plans and compound strategies as required for specific products within the Portfolio. S/he will manage successful cross-functional execution of the integrated project plans and specific compound strategies through proper management of cross-functional resources in various settings such as CDTs where relevant, smaller teams as is most efficient, and personal involvement with various strategic partners. This person will align the P/CDT to achieve its goals through the networks of people/functions represented on the team, participate in Portfolio Optimization activities, including new formulations, divesting/delisting, identify issues and leads contingency planning communicating to Senior Leadership, and work closely with the other P/CDTLs and TA Safety Heads and other groups within GMO in strategic planning and process improvements to maximize operational efficiency and ensure cohesive and coordinated approaches to best practices.
Qualifications
An MD is required. Subspecialty training is preferred. At least ten years of pharmaceutical industry experience overall and at least five years of clinical development experience and/or medical affairs experience is preferred. Pharmacovigilance is preferred. Experience on a Compound Development Team, a leadership role within a multi-functional R&D organization, ability to integrate all functional disciplines into a strategy and plan are all preferred. Expert knowledge of the global registration and commercialization is preferred. Strong problem-solving skills for developing creative solutions and meeting project objectives are required. Strong planning skills are required. Demonstrated influence, negotiation and conflict resolution skills, including the ability to influence with clear reporting authority are required. Strong oral and written communication skills are essential. This position is located in Titusville NJ, Raritan NJ, High Wycombe UK, Beerse Belgium, or Singapore Singapore. Up to 10% Travel domestic and international is anticipated.
BE VITAL in your career; be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W: LI NA
J2W:BIO
J2W:NSJ
J2W:MZ
Primary Location:North America-United States-New Jersey-Titusville
Other Locations:Europe/Middle East/Africa-United Kingdom-England-High Wycombe, North America-United States-New Jersey-Raritan, Asia Pacific-Singapore-Singapore-Singapore, Europe/Middle East/Africa-Belgium-Antwerp-Beerse
Organization: Janssen Research & Development, LLC. (6084)
Job Function: Clinical Research MD
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement
Senior Director, Woman's Health, Established Products Portfolio, Compound Development Team Leader-00000QGT
Description
Janssen Pharmaceutical Research & Development, L.L.C., a member of the Johnson & Johnson Family of Companies, is recruiting for a Senior Director, Womens Health, Established Products Portfolio/Compound Development Team Leader. This position will be based in Titusville NJ, Raritan NJ, High Wycombe UK, Beerse Belgium, or Singapore Singapore.
Janssen Research & Development, L.L.C. develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, and reproductive medicine.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
The Portfolio/Compound Development Team Leader (P/CDTL) is responsible for development and execution of the portfolio and compound strategies for multiple marketed products. The P/CDTL will directly supervise at least one Clinical Leader assigned to support the portfolio. Operational implementation is delivered through effective leadership of many cross-functional Compound Development Teams and the Portfolio, often including support for global registration and marketing efforts. The P/CDTL leads the team to support and develop products in a timely and cost effective manner, and is responsible for the execution of multiple compound strategies. Team leadership via matrix interactions includes individuals from line functions such as Clinical, Project Management, Global Regulatory Affairs, Pharmaceutical Development & Manufacturing Sciences (PDMS), Clinical Pharmacology, Global Strategic Marketing, Global Medical Safety, Janssen Supply Chain (JSC) , Drug Safety Sciences and other scientific and business related disciplines.
The Portfolio/Compound Development Team Leader (P/CDTL) actively contributes to Compound Strategy decisions of multiple CDTs by providing relevant strategic perspective, expertise and senior level guidance. S/he will lead the development and maintenance of the multiple integrated project plans and compound strategies as required for specific products within the Portfolio. S/he will manage successful cross-functional execution of the integrated project plans and specific compound strategies through proper management of cross-functional resources in various settings such as CDTs where relevant, smaller teams as is most efficient, and personal involvement with various strategic partners. This person will align the P/CDT to achieve its goals through the networks of people/functions represented on the team, participate in Portfolio Optimization activities, including new formulations, divesting/delisting, identify issues and leads contingency planning communicating to Senior Leadership, and work closely with the other P/CDTLs and TA Safety Heads and other groups within GMO in strategic planning and process improvements to maximize operational efficiency and ensure cohesive and coordinated approaches to best practices.
Qualifications
An MD is required. Subspecialty training is preferred. At least ten years of pharmaceutical industry experience overall and at least five years of clinical development experience and/or medical affairs experience is preferred. Pharmacovigilance is preferred. Experience on a Compound Development Team, a leadership role within a multi-functional R&D organization, ability to integrate all functional disciplines into a strategy and plan are all preferred. Expert knowledge of the global registration and commercialization is preferred. Strong problem-solving skills for developing creative solutions and meeting project objectives are required. Strong planning skills are required. Demonstrated influence, negotiation and conflict resolution skills, including the ability to influence with clear reporting authority are required. Strong oral and written communication skills are essential. This position is located in Titusville NJ, Raritan NJ, High Wycombe UK, Beerse Belgium, or Singapore Singapore. Up to 10% Travel domestic and international is anticipated.
BE VITAL in your career; be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W: LI NA
J2W:BIO
J2W:NSJ
J2W:MZ
Primary Location:North America-United States-New Jersey-Titusville
Other Locations:Europe/Middle East/Africa-United Kingdom-England-High Wycombe, North America-United States-New Jersey-Raritan, Asia Pacific-Singapore-Singapore-Singapore, Europe/Middle East/Africa-Belgium-Antwerp-Beerse
Organization: Janssen Research & Development, LLC. (6084)
Job Function: Clinical Research MD
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement