Eisai US
Associate Medical Director, US Oncology Medical Affairs - RCC
Eisai US, Nutley, New Jersey, us, 07110
Overview
At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisais human health care (hhc) mission. Were a growing pharmaceutical company focused on neurology and oncology, with a strong emphasis on research and development. Eisai seeks highly-motivated individuals who want to work in a fast-paced environment and make a difference. Responsibilities
Assists in the development of medical affairs strategy, planning and supportive tactics for the assigned therapeutic area. Under the direction of the Vice President, Medical Affairs, collaborates with key stakeholders to execute the medical affairs plan, including post-marketing research, congress management, medical education, research grants, medical advisory boards, and scientific communication/publication components of the medical operating plan. Leads country-level strategic development, planning, implementation, and oversight of Phase IIV clinical trial programs and early new product development within Medical Affairs for assigned product(s). Utilizes expert medical, clinical and scientific knowledge to provide tactical input for the development of product strategies and maintains relationships with external stakeholders to solicit feedback and strengthen Eisais medical reputation. Reviews and approves medical and scientific content of all relevant materials and communications. Participates in the design, strategies, planning and execution of Phase IV clinical development programs for assigned product(s). Creates IIS strategies and reviews proposals in conjunction with company policies. Participates in the review of CME grants. Serves as a medical resource providing direction for assigned products on key internal business processes, including active participation in relevant medical review committees. Supports timely and relevant communications with external customers, thought leaders, strategic alliances, key organizations, and institutions. Provides inputs to the development of budget and resources, including talent planning, and addresses deviations. May mentor, guide, and train new hires or less experienced colleagues. Qualifications
Advanced scientific degree (MD, PhD, PharmD) with 4+ years of experience in the pharma/biotech industry or academia, or a combination of equivalent education and experience. Practical knowledge of FDA regulations/ICH guidelines regarding conduct of clinical studies in oncology. Experience across Medical Affairs functions or phase II/III/IV clinical trials and diseases in the therapeutic area is preferred. Proven performance in earlier roles. Compensation & Benefits
The base salary range is 177,200232,600. Eisai offers participation in the Eisai Inc. Annual Incentive Plan and the Eisai Inc. Long Term Incentive Plan. Final pay determinations depend on factors including experience, education, knowledge, and skills. Employees are eligible to participate in company benefit programs. For information on benefits, visit https://us.eisai.com/careers-at-eisai/benefits. Some other benefits may be available; discuss with your recruiter. Eisai is an equal opportunity employer and is committed to recruiting, hiring, training, and promoting on all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Eisai prohibits discrimination based on disability, including disabled veterans, and provides reasonable accommodations where needed. Eisai participates in E-Verify. E-Verify is an Internet-based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Right To Work. Job details
Seniority level: Director Employment type: Full-time Job function: Health Care Provider Industries: Pharmaceutical Manufacturing
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At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisais human health care (hhc) mission. Were a growing pharmaceutical company focused on neurology and oncology, with a strong emphasis on research and development. Eisai seeks highly-motivated individuals who want to work in a fast-paced environment and make a difference. Responsibilities
Assists in the development of medical affairs strategy, planning and supportive tactics for the assigned therapeutic area. Under the direction of the Vice President, Medical Affairs, collaborates with key stakeholders to execute the medical affairs plan, including post-marketing research, congress management, medical education, research grants, medical advisory boards, and scientific communication/publication components of the medical operating plan. Leads country-level strategic development, planning, implementation, and oversight of Phase IIV clinical trial programs and early new product development within Medical Affairs for assigned product(s). Utilizes expert medical, clinical and scientific knowledge to provide tactical input for the development of product strategies and maintains relationships with external stakeholders to solicit feedback and strengthen Eisais medical reputation. Reviews and approves medical and scientific content of all relevant materials and communications. Participates in the design, strategies, planning and execution of Phase IV clinical development programs for assigned product(s). Creates IIS strategies and reviews proposals in conjunction with company policies. Participates in the review of CME grants. Serves as a medical resource providing direction for assigned products on key internal business processes, including active participation in relevant medical review committees. Supports timely and relevant communications with external customers, thought leaders, strategic alliances, key organizations, and institutions. Provides inputs to the development of budget and resources, including talent planning, and addresses deviations. May mentor, guide, and train new hires or less experienced colleagues. Qualifications
Advanced scientific degree (MD, PhD, PharmD) with 4+ years of experience in the pharma/biotech industry or academia, or a combination of equivalent education and experience. Practical knowledge of FDA regulations/ICH guidelines regarding conduct of clinical studies in oncology. Experience across Medical Affairs functions or phase II/III/IV clinical trials and diseases in the therapeutic area is preferred. Proven performance in earlier roles. Compensation & Benefits
The base salary range is 177,200232,600. Eisai offers participation in the Eisai Inc. Annual Incentive Plan and the Eisai Inc. Long Term Incentive Plan. Final pay determinations depend on factors including experience, education, knowledge, and skills. Employees are eligible to participate in company benefit programs. For information on benefits, visit https://us.eisai.com/careers-at-eisai/benefits. Some other benefits may be available; discuss with your recruiter. Eisai is an equal opportunity employer and is committed to recruiting, hiring, training, and promoting on all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Eisai prohibits discrimination based on disability, including disabled veterans, and provides reasonable accommodations where needed. Eisai participates in E-Verify. E-Verify is an Internet-based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Right To Work. Job details
Seniority level: Director Employment type: Full-time Job function: Health Care Provider Industries: Pharmaceutical Manufacturing
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