Pfizer, S.A. de C.V
Senior Medical Director, Late Development, Breast Oncology
Pfizer, S.A. de C.V, Tampa, Florida, us, 33646
Senior Medical Director, Late Development, Breast Oncology
Location: United States - Washington – Bothell, Pennsylvania – Collegeville, New York – New York City, Massachusetts – Cambridge, Connecticut – Groton
We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.
To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.
Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life‑changing medicines to the world.
Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.
Job Summary This position is for a Senior Medical Director within the atirmociclib program. The individual will support clinical trial(s) and lead sub‑teams in clinical development. The ideal candidate should have prior experience in clinical trials, supporting development programs, health authority interactions and demonstrate leadership to ensure the clinical development program meets scientific, ethical, and regulatory standards.
Job Responsibilities
Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring.
Lead peer‑to‑peer interactions with investigators.
Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities.
Lead and contribute to development and maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist and the cross‑functional team.
Provide clinical development leadership across several study teams.
Serve as the Clinical Development Lead on subteams including for Marketing Authorization Applications.
Collaborate with the Global Development Team to create and refine development strategies.
Represent the company in external engagements or as committee member in joint collaborations.
Collaborate with Clinical Scientists to review and interpret clinical data, identify key findings and implications, and communicate to internal and external stakeholders.
Maintain a high level of clinical expertise and professional competence by staying abreast of the latest developments, literature, and guidelines to advise on and drive current and future clinical development plans.
Basic Qualifications
Medical degree with 5+ years of industry experience.
Clinical oncology experience (typically 4+ years).
Preferred Qualifications Board certified/eligible in oncology or equivalent preferred.
Breast Oncology experience (2+ years).
Organizational Relationships Reports to Global Development Lead and partners closely with subject matter experts within cross‑functional study team, Pfizer Oncology Division and counterparts in other divisions within Pfizer.
Work Location Assignment This hybrid role requires you to live within commuting distance and work on‑site an average of 2.5 days per week.
Non‑standard Work Schedule, Travel or Environment Requirements Travel to scientific conferences / meetings several times per year, as needed.
Compensation and Benefits The annual base salary ranges from $242,000.00 to $403,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 25.0% of the base salary and eligibility to participate in our share‑based long‑term incentive program. Pfizer offers comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.
Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. (Additional details omitted.)
EEO & Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E‑Verify employer. This position requires permanent work authorization in the United States.
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We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.
To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.
Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life‑changing medicines to the world.
Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.
Job Summary This position is for a Senior Medical Director within the atirmociclib program. The individual will support clinical trial(s) and lead sub‑teams in clinical development. The ideal candidate should have prior experience in clinical trials, supporting development programs, health authority interactions and demonstrate leadership to ensure the clinical development program meets scientific, ethical, and regulatory standards.
Job Responsibilities
Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring.
Lead peer‑to‑peer interactions with investigators.
Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities.
Lead and contribute to development and maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist and the cross‑functional team.
Provide clinical development leadership across several study teams.
Serve as the Clinical Development Lead on subteams including for Marketing Authorization Applications.
Collaborate with the Global Development Team to create and refine development strategies.
Represent the company in external engagements or as committee member in joint collaborations.
Collaborate with Clinical Scientists to review and interpret clinical data, identify key findings and implications, and communicate to internal and external stakeholders.
Maintain a high level of clinical expertise and professional competence by staying abreast of the latest developments, literature, and guidelines to advise on and drive current and future clinical development plans.
Basic Qualifications
Medical degree with 5+ years of industry experience.
Clinical oncology experience (typically 4+ years).
Preferred Qualifications Board certified/eligible in oncology or equivalent preferred.
Breast Oncology experience (2+ years).
Organizational Relationships Reports to Global Development Lead and partners closely with subject matter experts within cross‑functional study team, Pfizer Oncology Division and counterparts in other divisions within Pfizer.
Work Location Assignment This hybrid role requires you to live within commuting distance and work on‑site an average of 2.5 days per week.
Non‑standard Work Schedule, Travel or Environment Requirements Travel to scientific conferences / meetings several times per year, as needed.
Compensation and Benefits The annual base salary ranges from $242,000.00 to $403,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 25.0% of the base salary and eligibility to participate in our share‑based long‑term incentive program. Pfizer offers comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.
Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. (Additional details omitted.)
EEO & Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E‑Verify employer. This position requires permanent work authorization in the United States.
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