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Medical Director

IQVIA Argentina

London

On-site

GBP 200,000 +

Full time

4 days ago
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Job summary

An established industry player is seeking a Medical Director to lead efforts in bringing innovative treatments for rare diseases to market in the UK. This role involves developing strategic medical affairs plans, engaging with healthcare professionals, and collaborating with cross-functional teams to ensure successful product launches. The ideal candidate will have a strong background in medical affairs, particularly within rare diseases, and will thrive in a dynamic, collaborative environment. If you are passionate about making a difference in patients' lives and have the expertise to drive medical strategies, this is an exciting opportunity for you.

Qualifications

  • Qualified Doctor of Medicine (MD) with 7-10 years in medical affairs.
  • Experience in rare disease therapy development and reimbursement pathways.

Responsibilities

  • Develop and implement the UK medical affairs plan focusing on pre-launch activities.
  • Engage with healthcare professionals and support real-world evidence programs.

Skills

Medical Affairs
Interpersonal Skills
Communication Skills
Project Management
Emotional Intelligence
Analytical Skills

Education

Doctor of Medicine (MD)
Master’s or Ph.D. in Pharmaceutical Science or Healthcare Management

Tools

Microsoft Excel
Microsoft PowerPoint

Job description

Medical Director, UK - Rare Diseases

This is an exciting opportunity to play a key role in bringing a life-changing treatment for Osteogenesis Imperfecta (and other rare diseases) to market in the UK working within a dynamic and collaborative environment. If you are an MD with experience in and passion for medical affairs and rare diseases, we encourage you to apply.

The successful candidate will play a pivotal role in developing and executing the UK medical affairs plan, collaborating closely with cross-functional teams and external stakeholders.

In this role, you will work closely with the Head of Medical Affairs to ensure the successful delivery of pre-launch and launch activities, including scientific interactions, real-world evidence programs, and medical strategy development.

Key Responsibilities:

  1. Develop and implement the UK medical affairs plan with a primary focus on pre-launch activities for OI.
  2. Refine and execute the mapping of OI treatment centers, identifying key hubs and spokes, and collaborating with the Country Patient Access Lead to gather detailed insights into patient numbers, treatment pathways, and the overall OI landscape.
  3. Conduct field scientific interactions with healthcare professionals (HCPs) ensuring compliance with local regulations and guidelines.
  4. Support the SATURN Real World Evidence (RWE) Program in alignment with global medical strategies.
  5. Attend local OI scientific meetings, engage with Key Opinion Leaders (KOLs) and HCPs, and seek opportunities to present relevant scientific publications in line with the broader scientific communications strategy.
  6. Participate in Early Scientific Advice meetings, collaborating with local teams to prepare materials and present the medical strategy.
  7. Work closely with the Patient Access Lead to engage KOLs in dossier strategy development and support key stages of the reimbursement process, including hearing preparations.
  8. Contribute to specific Patient Access Strategy Plan, ensuring alignment between medical and patient access teams for the successful launch of the OI treatment.

Qualifications and Experience:

  1. Qualified Doctor of Medicine (MD).
  2. Additional qualifications such as a university degree, Master’s, or Ph.D. in pharmaceutical science, healthcare management, or a related field are an advantage.
  3. 7-10 years of experience in medical affairs, preferably in a biotech or pharmaceutical company.
  4. Knowledge of the healthcare systems within the UK, with experience in the reimbursement pathway being an advantage.
  5. Proven track record of working in rare disease therapy development, with hands-on experience in medical affairs strategy and delivery during late-stage development and launch.

Personal Attributes:

  1. Ability to work effectively within a cross-functional, matrix environment, contributing both to strategic planning and hands-on execution.
  2. Strong interpersonal and communication skills, with demonstrated experience working across international teams to deliver high-quality results.
  3. High emotional intelligence (EQ) with the ability to build trusted, long-term relationships within rare disease communities and across diverse stakeholders.
  4. Entrepreneurial mindset with the ability to innovate and shape new markets, particularly for therapies where no current alternatives exist.
  5. Self-motivated with a proactive, "can-do" attitude and a collaborative, low-ego team ethos.
  6. Strong organizational skills, with the ability to manage multiple projects while respecting timelines and deadlines.
  7. Excellent communication with experience presenting complex information to various audiences.
  8. Proficiency in Microsoft Office, especially Excel and PowerPoint, with strong presentation and analytical skills.
  9. Willingness to travel as needed and participate in face-to-face team meetings.

Please note: Sponsorship is not available for this opportunity.

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