The Clinical Reporting unit at Novo Nordisk has rapidly grown into an integral part of the Global Clinical Reporting community since its inception in 2011. The team consists of skilled Medical Writers, Publishers, and Document Controllers with expertise in various therapeutic areas and regulatory requirements. The team’s scientific expertise drives clear and impactful communication on the conduct and outcome of clinical trials, significantly contributing to Novo Nordisk’s regulatory commitments.
Qualifications:
- Education: PhD, MSc, M.Pharm, or equivalent.
- Experience: 10+ years in medical writing or relevant work experience, particularly in regulatory medical writing.
- Skills:
- Strong understanding of clinical development and regulatory processes.
- Experience working in a global setting, preferably within the pharmaceutical/CRO industry.
- Excellent analytical, communication, and presentation skills.
- Ability to manage multiple tasks simultaneously, with a proven track record of delivering high-quality work on time.
- Committed, persistent, and proactive in driving project strategies.
Working at Novo Nordisk:
Novo Nordisk is a leading global healthcare company with a century-long legacy of addressing serious chronic diseases. With a workforce of over 63,000, Novo Nordisk impacts the lives of over 40 million patients daily. The company values diverse perspectives and fosters an inclusive culture that celebrates the diversity of its employees, patients, and communities.
