(Senior) Global Medical Advisor (m/f/d) - Immunotherapy

Octapharma Austria; Wien; On-site; EUR 44,000 - 53,000; Full time

Benefits offered by this job

Company restaurant

Meal subsidy

Training & development

Health promotion

Parking and transport access

Company events

Job summary

Octapharma Austria, Vienna, Permanent position in Global Medical & Scientific Affairs, seeks a medical affairs professional with a PhD/MD background to oversee regulatory writing and clinical development support.

You will revise medical documents, answer clinical inquiries, manage literature databases, and coordinate publications for trials. Fluency in English is required; travel is expected. The role offers strong development in a global pharma environment.

Qualifications

• MD or PhD with medical/scientific background.
• Experience in immunology, regulatory procedures, clinical development.
• 5+ years in the pharmaceutical industry.
• Advanced writing and researching in medical databases.
• Fluent English; other languages helpful.
• Excellent organizational skills.
• Strong interpersonal communication.
• Willingness to travel.

Responsibilities

• Medical revision and compilation of outgoing texts (PIL, PI, SPC, DSURs/PSURs).
• Answer medical enquiries related to Octapharma products.
• Maintain database for medical enquiries.
• Maintain in-house literature database.
• Manage publications for clinical studies by Octapharma.
• Collaborate with internal stakeholders and departments.
• Support Octapharma activities at international congresses.
• Approve marketing materials.
• Oversee Phase IV programs.

Skills

MD/PhD background

Immunology

Regulatory procedures

Clinical development

Scientific writing

Medical databases

Fluent English

Other languages beneficial

Organizational skills

Interpersonal communication

Travel readiness

Education

MD or PhD

Job description

Job-ID: 63329

Location: Wien, AUT

Job Level: Professionals

Category: Medical Affairs

Employment Type: Permanent position

Become part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation. With over 1700 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location.

Your Main Tasks And Responsibilities

• Medical revision and compilation of outgoing text documents (e.g. PIL, PI, SPC, DSURs/PSURs)
• Answering of medical enquiries associated with the use of any of the company’s products
• Maintenance of a database for medical enquiries
• Supervision and maintenance of the in-house literature database
• Managing the publications process related to clinical studies conducted by Octapharma
• Close collaboration with different internal stakeholders and departments
• Support of Octapharma activities at international congresses
• Approval of marketing materials
• Overview of phase IV programs

Your expertise and ideal skill set

• Completed academic degree, ideally in a medical or scientific background (MD or PhD)
• Experience in immunology, regulatory procedures, clinical development
• At least 5 years of working experience in the pharmaceutical industry
• Advanced skills in scientific writing and researching in medical databases
• Fluent English, additional languages beneficial
• Excellent organizational skills
• Strong interpersonal communication skills
• Readiness to travel

Your department - where you make an impact

• At Global Medical & Scientific Affairs, we turn scientific knowledge into meaningful impact by bridging clinical research and real-world care, empowering healthcare professionals worldwide to deliver better outcomes for patients.

Thrive with us

• Company restaurant & meal subsidy
• Training & further education
• Health promotion
• Parking spaces and good public transport connections
• Company and team events

Benefits

Enjoy these attractive benefits! You can find all offers here: The minimum gross salary according to the collective agreement (chemical industry) is EUR 4.355,55 based on 38 hours per week (full-time). As we strive to offer a salary that reflects your individual profile and qualifications, there is a willingness to pay above the minimum salary.

It´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. Johanna Proksch, MA

Octapharma Pharmazeutika Produktionsges.m.b.H.

Oberlaaer Straße 235, 1100 Wien

T: [phone] - 4299

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 with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 200 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide.