Your main tasks and responsibilities
- Responsible for project management of NIS and IIS
- Manage the publication processes related to clinical studies conducted by Octapharma
- Literature research on Octapharma's products, competitor products and indications thereof for :
Product reviews for submissions to international health-authorities
Response to internal scientific questionsResponse to external medical enquiriesMaintenance of the in-house literature databaseDissemination of relevant medical content to internal stakeholdersRespond to medical enquiries and maintain & expand global medinfo databaseIdentify KOLs and establish & maintain contact in collaboration with IBU and respective countryActively support, assimilate and report content of relevant international congresses and act as the onsite medical affairs representative at congressesMedical revision and compilation of outgoing text documents with international or national reach (e.g. PIL, PI, SPC, DSURs / PSURs) in close collaboration with Regulatory and Clinical Research Departments and Corporate Drug Safety Unit (CDSU)Revision and approval of marketing materials in collaboration with IBUInterface to internal departmentsOccasional : Staff Training on indications and medical background of Octapharma's productsYour expertise and ideal skill set
Completed academic degree, ideally in a medical or scientific background (MD od PhD)Must have demonstrated senior authority and confidence in dealing with specialist divisions like business units, drug regulatory affairs and external stakeholders (eg KOLs, Regulatory Authorities)Over 10 years knowledge of the pharmaceutical industry or of pharmaceutical service industry5 years experience in Plasma industry preferableAdvanced skills in scientific writing and researching in medical databasesVery good English(C1), additional languages beneficialExcellent organizational skillsStrong interpersonal communication skillsReadiness to travelGood IT skillsYour department - where you make an impact
GMSA turns scientific knowledge into meaningful impact by bridging clinical research and real-world care, empowering healthcare professionals worldwide to deliver better outcomes for patients.
The Medical Advisor serves as a key scientific and clinical expert within the organization, bridging the gap between clinical practice and pharmaceutical development. This role supports the medical and strategic objectives of the company by providing evidence-based medical insights, ensuring scientific accuracy, and promoting the safe and effective use of the company's products.
Thrive with us
You help save lives - Every day is meaningful as we produce life-saving medicinesFamily values - Long-term perspective for employees and relationshipsBe rewarded with market-related salary and benefits packageYou will have a high level of influence where you can make a difference and leave your footprintWork with skilled and fun colleagues in a relatively informal organizationSkills development - We offer various internal and external employee and leadership trainings, trainee programs and digital solutionsIt´s in our blood
We live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion.
Do you have any questions? Then get in touch with your contact person.
Mrs. Claudia Vignau
Octapharma AG
Seidenstrasse 2, 8853 Lachen
T : +41 55 451 21 35
Want to find out more about us?
Visit our website Octapharma Career and follow us daily on LinkedIn .
About Octapharma
Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries wi j4id10036980a j4it0103a j4iy26a