Global Medical Affairs Lead

Octapharma Austria; Wien; Vor Ort; EUR 44.000 - 53.000; Vollzeit

Benefits dieser Stelle

Company restaurant

Meal subsidy

Training & development

Health promotion

Parking and transport access

Company events

Zusammenfassung

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.

Qualifikationen

• 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.

Aufgaben

• 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.

Kenntnisse

MD/PhD background

Immunology

Regulatory procedures

Clinical development

Scientific writing

Medical databases

Fluent English

Other languages beneficial

Organizational skills

Interpersonal communication

Travel readiness

Ausbildung

MD or PhD

Jobbeschreibung

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.