Associate Director, Global RWE (Real World Evidence), Global Medical Affairs - Neurology

Eisai Inc.
New Jersey, Princeton
Full-time

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission.

We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development.

Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease.

As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference.

If this is your profile, we want to hear from you.

Summary

The Associate Director is responsible for developing RWE strategies for assigned product(s) and execution of RWE research for the development and communication of product value data to support Eisai business.

This role primarily focuses on late-stage pipeline and marketed products, interfaces with cross-functional teams including US medical affairs, marketing, market access global value and access teams, commercial to align strategies in customer research activities and development of external communication materials.

Responsibilities

  • Support formulation and implementation of Global RWE strategies aligned with the functional, business and patient needs to develop a compelling value proposition that drives optimal access and utilization of Eisai marketed products.
  • As needed, take on responsibility for oversight of vendors selected to manage ongoing RWE efforts, including Ph4 study management, and presentations and publications emanating from these efforts
  • Actively collaborate with cross-functional teams (e.g., US medical affairs, marketing, market access global value and access teams, commercial) to prioritize projects towards achieving effective utilization of resources.
  • Demonstrate product differentiation and value to support, value and access, health outcomes and safety needs.
  • Draft communication / publication strategies for given products and publication / presentation of RWE related research outcomes at internal and external forums.
  • Generate evidence to support Eisai’s recognition as a trusted advocate for patient access to appropriate therapeutic alternatives.
  • Keep up to date with current methodological, clinical practices and professional guidelines to support decision-making towards meeting the needs of patients, providers and payers, as well as optimize access to Eisai’s products and appropriate medical care.
  • Provide oversight to external partner / vendor deliverables in line with defined objectives and scope for assigned products, and address critical escalations as warranted.
  • May provide mentoring, guidance and training to new hires / less experienced colleagues.

Qualifications

  • Masters or Doctoral (preferred) degree in health services research, public health, medicine, epidemiology, or related field with 5+ years of relevant experience in real world evidence generation / outcomes research / or closely related discipline either within biopharmaceutical
  • Experience in designing, analyzing and collecting RWD using EMRs, patient charts, administrative claims datasets.
  • Previous RWE experience in medical or clinical development, and interactions with regulatory authorities is desirable.
  • Experience with launch of products and working on pipeline and marketed products is preferred with emphasis on dengerative disease
  • High competence in design and execution of RWE studies (in partnership with thought leaders in major geographic regions of Eisai business), including developing protocols and analytic plans for prospective and retrospective studies.
  • Strong scientific communication record in terms of conference presentations and manuscripts is desirable.
  • Relevant academic training and prior experience in conducting health economic modeling, health-related quality of life, and / or health services research studies.
  • Proven ability to develop professional relationships with healthcare stakeholders, key opinion leaders, peers and of working in alliance / co-promotion settings and / or leading cross-functional teams.
  • Some experience of managing / leading teams directly / indirectly or coaching and mentoring new hires / less experienced colleagues.
  • Previous experience in vendor management and budget management including cross-functional communication with ability to influence without authority.
  • Proven performance in earlier role.

LI-MI1

IND123

LI-Remote

Eisai Salary Transparency Language :

The base salary range for the Associate Director, Global RWE (Real World Evidence), Global Medical Affairs - Neurology is from : 181,000-237,600Under current guidelines, this position is eligible to participate in : Eisai Inc.

Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan.

Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.

Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit .

Certain other benefits may be available for this position, please discuss any questions with your recruiter.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in 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.

Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.

Eisai Inc. 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.

Please click on the following link for more information :

29 days ago
Related jobs
Promoted
Genmab
Hamilton Township, New Jersey

Director will work as an integral part of the Medical Affairs Strategy Team in close alignment with Global Medical Affairs Strategy Lead and the cross-functional medical affairs cross functional partners, providing input and strategic direction for the program. Reporting to the Global Medical Affair...

Promoted
Sun Pharmaceutical Industries, Inc.
Harlingen, New Jersey

Innovation Summary:The Director, Medical Affairs NA - Biologics Lead will report to the AVP, Medical Affairs NA - Biologics and Market Access, and be a key medical resource in developing and implementing the medical affairs strategy for biologics. Among the responsibilities, the Director will active...

Promoted
Genmab
Hillsborough Township, New Jersey

Director will work as an integral part of the Medical Affairs Strategy Team in close alignment with Global Medical Affairs Strategy Lead and the cross-functional medical affairs cross functional partners, providing input and strategic direction for the program. Reporting to the Global Medical Affair...

Promoted
Sun Pharmaceutical Industries, Inc.
Harlingen, New Jersey

Innovation Summary:The Director, Medical Affairs NA - Biologics Lead will report to the AVP, Medical Affairs NA - Biologics and Market Access, and be a key medical resource in developing and implementing the medical affairs strategy for biologics. Among the responsibilities, the Director will active...

Promoted
Global Channel Management
Raritan, New Jersey

Medical Technologist Specialist needs 1-3 years' experience within a cGMP environment. Medical Technologist Specialist requires:. A Bachelor's degree in Medical Technology, Biology or a related field of study. Medical Technologist Specialist duties:. ...

Promoted
Sun Pharmaceutical Industries, Inc.
Ten Mile Run, New Jersey

We manufacture, market and distribute pharmaceuticals to the world’s largest wholesalers, distributors, warehousing and non-warehousing chain drugstores as well as managed care providers. We are proud that our global workforce is bound by our common values:Humility. This position reports directly to...

American Medical Associates
Plainsboro Township, New Jersey

American Medical Associates -. Assistant Director of Nursing - LTC - Plainsboro Township, NJ. Requirements of the Assistant Director of Nursing:. Must have prior exeprience as an Assistant Director of Nursing. ...

SUN PHARMA
Princeton, New Jersey

The Medical Affairs Director Biologics will report to the AVP, Medical Affairs Biologics, as a key medical/scientific resource in the development and implementation of the medical affairs strategy for dermatology. Among these responsibilities, the Medical Affairs Director will actively manage, lead,...

Bristol Myers Squibb
US,NJ,Giralda,Madison

Establishing a clear, viable and compelling strategy for the Medical Communications, aligned with overall Medical vision, strategy and objectives, and ensure delivery of timely and high-quality medical publications, scientific content, medical education, medical information, and congress presentatio...

Capleo Global LLC
Edison, New Jersey

It is anticipated the Senior Project Director will be required throughout all phases of work within the portfolio. Enhancement of provincial Electronic Health Record (EHR) and Electronic Medical Record (EMR) systems and services. Demonstrated experience in a role contributing to the development or i...