Regulatory affairs director Jobs in Zürich

POSITION SUMMARY

As an integral member of the global Sickle Cell Disease team reporting to the Global Medical Affairs Team Lead Sickle Cell Disease you will contribute to the development of the global medical strategy and tactical execution for Sickle Cell Disease (SCD) focusing on Voxelotor.

KEY RESPONSIBILITIES

Work closely with cross-functional colleagues from Medical Affairs Global Product Development Biostatistics Regulatory Affairs Safety Commercial and Market Access to ensure that the Sickle Cell Disease (SCD) global medical strategy / tactical and evidence generation plans with a primary focus on Voxelotor optimally address current and future needs.

Lead the Voxelotor publications subcommittee and act as overall SCD publication lead to plan and implement appropriate publication strategies and tactics in accordance with Pfizer policy.

Work with the publication process including concept author and agency liaison publications subcommittee review and allowing for promotional use if appropriate

Establish how the medicines profile fits into customer needs and the commercial strategy and compares to competitive medicines effectively communicating same to various stakeholders including patients.

Development review and approval of internal and external medical materials; review and approval of commercial materials training of medical and XFT colleagues

Lead support and coordinate external medical communication initiatives via symposia proactive / reactive medical communication etc.

Collaborate with colleagues in Medical Affairs to ensure all communications are aligned with the medical strategy with the patient at the heart of everything we do

Partner with Patient Advocacy to develop research studies to understand the patient and caregiver perspective around burden of disease and treatment outcomes

Partner with Global Access Strategy & Pricing colleagues to prepare reimbursement dossiers as appropriate

Contribute to GMAT and GMAT sub-committees (Evidence Generation; Medical Insight and Impact; Medical Engagement) as appropriate

Collaborate with external study investigators patient groups and other consortia to maximize synergies in development of and access to complementary data

Proactively bring patients & physicians voice to medical affairs efforts on cross-functional teams while considering the needs of SCD providers and payers.

Participate in the ongoing assessment of the benefit-risk of the medicines taking into account new data as it becomes available.

Provide consultation & contribute to the planning and timely high-quality execution of medical tactics to support the Countries and Regions and lifecycle plan.

Participate in the effective communication of current scientific knowledge including medical needs to different stakeholders including patients customizing the communication for the audience leading to effective communication.

Serve on working groups in a professional inclusive manner encouraging open discussion as related to assigned activities and specific roles while demonstrating respect for all people.

Support the organization of global external meetings including advisory boards congresses and symposia as appropriate

Educate concerning medicine and / or therapeutic expertise to other medical and non-medical team members including Sale Force / country medical colleagues.

Address potential medical issues and ensure implementation of risk-management strategies in collaboration with team partners.

MINIMUM REQUIREMENTS

PharmD or PhD and 5 years of medical affairs experience

Experience objectively interpreting and analyzing medical and scientific data

Experience defining and communicating complex scientific and medical concepts to internal and external stakeholders

Excellent verbal communication and presentation skills

Experience prioritizing multiple demands

Experience effectively leading in a matrix organization

Up to 25% international travel

PREFERRED QUALIFICATIONS

International experience

Sickle Cell Disease therapeutic area experience

Candidate demonstrates a breadth of diverse leadership experiences and capabilities including : the ability to influence and collaborate with peers develop and coach others oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

Work Location Assignment : This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week.

Medical

Required Experience :

Director

Key Skills

Apache,Control System,Data Structures,Hotel Front Office,Clinical

Employment Type : Full-Time

Experience : years

Vacancy : 1