Senior Medical Director TTR – Mid-Sized Markets – International

Job title:

Senior Medical Director TTR – Mid-Sized Markets – International

Company:

Alnylam Pharmaceuticals

Job description

Job Description:OVERVIEWMedical Affairs International TTR stands for integrity through unbiased, objective and balanced medical-scientific dialogs with the medical community. It plays a strategic role in a matrix of major responsibilities.The Senior Medical Affairs Director International Mid-size Markets (MSM) TTR reports into the Vice President, Head Medical Affairs International TTR.The MSM country Medical Affairs Directors TTR report into the Senior Medical Affairs Director MSM TTR.The Senior Medical Director is the regional medical-scientific lead responsible to ensure scientific excellence.This individual is an active member of the international Medical Affairs Leadership and the MSM Leadership Teams .The successful candidate will be accountable for the development and the implementation of the long and short-term MSM Medical Affairs TTR cardiomyopathy and polyneuropathy strategy and action plans in collaboration with the MSM countries, International and Global Medical TTR teams/leaders related to:

• Evidence generation
• Eviden dissemination – including HCP education programs
• Key thought leader engagement programs
• Operational excellence

KEY RESPONSIBILITIESMEDICAL AFFAIRS MSM TTR TEAM LEADERSHIP

• Provides leadership to the MSM countries’ Medical Heads and oversight of the MSM countries’ Medical Affairs Teams.
• Attracts, retains, and develops Medical Affairs MSM TTR talent, ensuring that each team member has regular performance reviews, receives timely feed-back and has specific development plans that are implemented in a timely manner.
• Sets performance metrics for country Medical Affairs Teams ensuring execution of local Medical Affairs plans.

CROSS-FUNCTIONMAL COLLABORATION

• Contributes to the development of the MSM Business strategy (including the Medical Affairs one).
• Partners with the Head of MSM Business to appropriately enable commercial success.
• Provides Medical Affairs expertise as needed to assist in the development and execution of compliant commercial activities.
• Partners with country, MSM regional and International stakeholders, both externally and internally to support reimbursement applications and patient access.
• Represents Medical Affairs in pricing and reimbursement teams and meetings and closely collaborates with market access and other relevant country stakeholders.

EVIDENCE GENERATION

• Ensures development and implementation of post-approval evidence generation (e.g. phase 4, investigator-initiated studies, collaborative studies, chart reviews) in the MSM region alligend with Global and International evidence generation strategy to address strategic data gaps (e.g. payer data needs).
• Partners with Global and International Medical Affairs Teams and other R&D functions to provide Medical Affairs input on clinical trial design and supports clinical trial enrolment.
• Partners with key stakeholders to define operating principles to guide evidence-based Medical Affairs activities and ensure all activities are compliant with local laws and regulations

BUDGET MANAGEMENT

• Oversees MSM countrie’s Medical Affairs budget and resource allocation with utmost accuracy.

COMPLIANCE

• Ensures compliance with all applicable laws and regulations

QUALIFICATIONS

• M.D. (Medical Doctor) and/or PhD and/or equally qualified academic healthcare professional with proven enterprize, strategic, team and personal leadership experience in the Pharmaceutical or Biotechnology industry. Medical degree and experience in cardiology preferred.
• Strategic thinker with excellent problem solving and decision -making skills, ideally with product launch experience.
• Resilient self -starter, who can act independently and learn quickly.
• Team builder, capable of interacting effectively with external medical contacts and at every level within the company.
• Broad understanding of the regulatory environment in the region and direct experience in the P&R processes.
• Extensive cross-functional project leadership experience and ability to operate effectively in a complex matrix organization.
• Perceptive, creative person with the ability to contribute new ideas and to build consensus.
• Business acumen, demonstrating desire to work in a fast-growing environment
• Ability and willingness to travel including during week-ends (min. 25%)

About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by “interfering” with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality.Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we’ve been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as one of Science Magazine’s Top Biopharma Employers, one of America’s Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK – among others.At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients.

Expected salary

Location

Nederland

Job date

Sun, 15 Dec 2024 08:25:23 GMT

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