Scientific Director US Medical Affairs, Pulmonary Hypertension

3 days ago


Cary NC United States Chiesi Farmaceutici S.p.A. Full time
Scientific Director US Medical Affairs, Pulmonary Hypertension

Department: Medical Affairs

Job Type: Direct Employee

Team: Mktg, Market Access, Bus. Excellence & Med. Affair

Contract Type: Permanent

Location: Cary, NC, US

About us

Based in Parma, Italy, Chiesi is an international research-focused pharmaceuticals and healthcare group with over 85 years’ experience, operating in 30 countries with more than 6,000 employees (Chiesi Group). To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group research, develops and markets innovative drugs in its three therapeutic areas: AIR , RARE , and CARE .

We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification , a recognition of high social and environmental standards. We are committed to embrace diversity, inclusion and equal opportunities.

Chiesi USA

Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent specialty and rare disease markets. We are a B Corp and Benefit company awarded Top Employer status for six consecutive years and certified as a Great Place to Work.

What we offer

Chiesi offers competitive benefits, services, and programs that enrich the personal and professional lives of our employees.

Purpose

The primary responsibility of this role is to lead the development, execution, and implementation of the global Medical Affairs strategy for Seralutinib within the US market in partnership with Gossamer Bio, our Alliance Partner.

Main Responsibilities
  • Drives the development and execution of the global medical strategy for Seralutinib in close partnership with the alliance partner and the ROW Medical Affairs Head.
  • Incorporates insights from the ROW Medical Affairs Head to ensure the global strategy is comprehensive and reflective of ROW market perspectives.
  • Aligns medical and scientific initiatives with Scientific Communication Platform and contributes to the development of and execution of the Medical Education, Advisory Boards and External Engagement Plan.
  • Partners with the ROW Medical Head to co-create, integrate, and complement these initiatives with ROW efforts.
  • Oversees the US Conference planning and execution.
  • Map Patient Journeys for Seralutinib in the US, identifying key patient needs and apply the framework to the possible solutions, collaborating with commercial, market access, and the alliance partner.
  • Responsible for performing the accurate and detailed medical review of complex advertising and promotional materials in accordance with established policies and practice standards.
  • Co-Leads the development of the global evidence generation plan, partnership with the Alliance Partner and the ROW Medical Affairs Head to integrate insights from ROW markets.
  • Contribute to the Investigator Initiated Study (IIS) and educational grants strategy and reviews and makes recommendations regarding submitted proposals.
  • Co-leads the global publications strategy alongside the alliance partner, while developing a tailored publication plan for the US.
  • Participates in the Medical Affairs Respiratory Team, providing medical input on US labeling and regulatory interactions.
  • Collaborates with clinical operations and teams to support US clinical studies.
  • Acts as an active member of the Core Team conducting medial activities and planning for the US in partnership with the alliance partner.
  • Single Point of Contact for Gossamer Medical Affairs.
  • Develops and implements effective alliance processes for medical affairs.
Experience Required
  • A minimum 7+ years Pharmaceutical Industry experience and at least 5 years of relevant work experience in the US and in the pulmonary hypertension therapeutic area.
  • Demonstrated ability to think and act strategically, with demonstrated tactical execution.
  • In-depth knowledge of Pulmonary Hypertension with expert insight to drive the disease vision through rigorous scientific debates with medical thought leaders.
  • Ability to influence, work and align with multiple Chiesi-internal and external stakeholders.
  • Experience working with alliance partnerships and co-promotion setups.
  • Prior experience working on a launch product for pulmonary hypertension is preferred.
  • Understanding of HCP, Payer, and Policy Maker informational needs.
  • Proven planning and organizational skills with great attention to detail.
  • Knowledge of clinical trial methodology, regulatory requirements governing clinical trials is preferred.
  • Strong interpersonal skills in developing and maintaining successful stakeholder relationships.
  • Excellent written and oral communication skills.
  • Understanding of global markets, including ROW regulations and market dynamics.
  • Innovative thinker with a passion for adopting emerging technologies.
Education

Completion of a graduate level degree (PharmD, MD, DO, DNP, PhD, MSN, MS)

Chiesi USA is an equal opportunity employer committed to hiring a diverse work force at all levels of our business.

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