As our Head of Medical Safety GCSP, you will be accountable for all medical safety related aspects of clinical safety and pharmacovigilance as well as ad hoc safety issues and innovation projects in your area of expertise. In this role, you will manage and mentor a team of six (Sr) Safety Physicians and (Sr) Safety Scientists. Key responsibilities
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What you bring
To become a success in this role, you bring a Medical Doctor (MD) degree combined with leadership experience within clinical safety and pharmacovigilance. You are recognized for setting direction, taking accountability, and leading teams with passion, clarity and empathy in a highly regulated, global environment. You balance strategic oversight with confident decision?making and strong ethical stakeholder engagement. •
10+ years of parcours professionnel across clinical safety and pharmacovigilance, including senior Medical Safety roles
You bring solid knowledge of global clinical safety and pharmacovigilance regulations including GCP, GVP, and ICH guidelines, along with hands-on experience in CTD compilation and MAAs/BLAs sub
MISSIONS
to major health authorities. Besides this, you communicate fluently in English with solid written, verbal, and presentation skills using medical and regulatory terminology. You are highly proficient in relevant IT tools and database applications and are a self-driven, positive team player who helps to build and sustain high performance and team cohesion. Most importantly, you thrive in change; your judgment, integrity, and resilience help safeguard patient safety and support our transition from development to full commercialization in a fast-moving, life-science environment. Please note an advanced degree is required, and an MD
QUALIFICATIONS
is mandatory for this role. Why this role
This role offers a unique opportunity to take end?to?end responsibility for all medical safety activities within clinical safety and pharmacovigilance in a science driven organization with a strong purpose. You will mentor a team, work closely with global stakeholders, contribute directly to regulatory sub
MISSIONS
and patient safety, and have real influence on how safety processes and risk management activities are shaped and executed. It is a role with both strategic impact and hands?on responsibility, ideal, if you want to grow your expertise while making a meaningful difference. In this role, you will have the platform to make a lasting impact on public health, advance our
MISSIONS
, and set new benchmarks for medical excellence in a dynamic, growth-oriented biotechnology environment. Application
If you are ready to take on a pivotal role in a growing organization and drive meaningful change in healthcare, apply now and join Bavarian Nordic in our
MISSIONS
to improve health outcomes and foster sustainable growth. Please note that we do not support any relocation package for this role. We kindly request that headhunters or recruitment agencies refrain from contacting us regarding this position. Bavarian Nordic is a global vaccine company with a
MISSIONS
to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America. Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For more information, visit www. bavarian-nordic. com
Bavarian Nordic
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Profil recherché
is mandatory for this role. Why this roleThis role offers a unique opportunity to take end?to?end responsibility for all medical safety activities within clinical safety and pharmacovigilance in a science driven organization with a strong purpose. You will mentor a team, work closely with global stakeholders, contribute directly to regulatory sub