Associate Director, Head of Medical Affairs and Regulatory/Pharmacovigilance

Category:  Clinical Development
Location: 

Manila, National Capital Region, PH

 

Are you passionate about medical affairs and regulatory strategies? Do you have a knack for driving scientific communication and ensuring regulatory success and compliance? If so, you might be the perfect fit for our Head of Medical Affairs and Regulatory/ Pharmacovigilance position (RA/PV) in the Philippines! Read more and apply today for a life-changing career. The position is located in Manila, Philippines.

 

Your new role

 

As the Head of Medical Affairs & RA/PV, you are part of the affiliate Leadership Team. You will play a pivotal role in driving scientific communication and regulatory compliance in the Philippines. Your input and voice are critical in shaping the strategic direction of the affiliate together with the rest of the Leadership Team. You contribute to both short-term and long-term strategy as well as execution to ensure sustainable business growth and organizational success.

 

As the Head of Medical Affairs & RA/PV, you will be responsible for:

  • Bring medical and regulatory insights and perspective to contribute to affiliate near- and long-term strategic planning.
  • Lead and deliver timely, accurate and credible scientific communication in the Philippines, ensuring consistency and high standards across all channels and audiences.
  • Establish and maintain strong KOL governance and scientific engagement with top local authorities to support evidence-based dialogue and trust.
  • Build and disseminate scientific and medical knowledge internally and externally, fostering cross-functional communication and relationships with the broader scientific community.
  • Drive education initiatives for commercial, medical and regulatory/pharmacovigilance teams, coordinate publication and congress strategies, and represent the organization at scientific meetings to amplify research findings and clinical insights.
  • Align and coordinate local implementation of global and regional medical strategies with the national product and project plans.
  • Oversee regulatory submission, monitoring/pharmacovigilance operations and compliance, nurturing trusted relationships with local health authorities to secure and maintain licenses to operate; Lead the patient safety function to establish and maintain pharmacovigilance and medical device vigilance systems that meet global, local and external regulatory requirements.

 

Your new department

 

The Medical Affairs & RA/PV department at Novo Nordisk Philippines is at the forefront of scientific communication and regulatory compliance. Based in the Philippines, our team is dedicated to ensuring the highest standards of medical and regulatory/pharmacovigilance excellence. We work in a fast-paced and dynamic environment, fostering collaboration and innovation to make a real difference in patients' lives. Join us and be part of a team that is passionate about driving change and delivering results.

 

Your skills and qualifications

 

  • Must be a licensed physician or must have a biomedical sciences degree. Postgraduate qualification desirable.
  • Minimum 10 years of industry experience in medical affairs function, ideally in related therapeutic areas, and must have at least 5 years in a managerial role.
  • Experience in defined therapy areas (desirable): Diabetes, Obesity, CV, other Endocrine-related disorders.
  • Understanding of the Philippine healthcare structure and regulatory/pharmacovigilance environment will be a significant advantage.
  • Excellent verbal and written communication skills.

 

Working at Novo Nordisk

 

For over 100 years, we've been driven by a singular purpose: to defeat serious chronic diseases and create lasting change for long-term health. This dedication shapes everything we do, from the way we approach challenges with curiosity and determination, to how we collaborate with mutual respect and shared purpose. Here, you'll be part of a culture where diverse perspectives are valued, innovation is encouraged, and every contribution matters. When you join Novo Nordisk, you're not just advancing your career – you're becoming part of a story that transforms millions of lives across generations.

What we offer

 

Being part of a global healthcare company means opportunities to learn and develop all around you. You'll experience our investment in your personal and professional growth, benefit from cross-functional exposure, and work within a culture that values your wellbeing and career aspirations. Our benefits are designed with your career stage and life needs in mind, supporting you to perform at your best while creating meaningful impact.

 

Deadline

 

Until the completion of recruitment. Applications are reviewed on an ongoing basis so you are encouraged to apply as soon as possible.

 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

 

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.