(Senior) R&D Project Manager (f/m/d) - Pharma

Eblinger & Partner; Wien; Vor Ort; EUR 63 000; Vollzeit

Zusammenfassung

Ein dynamisches Unternehmen in der Pharmaindustrie sucht einen (Senior) R&D Project Manager, der die Verantwortung für die Leitung komplexer Entwicklungsprojekte übernimmt. Diese Rolle erfordert eine Kombination aus wissenschaftlichem Verständnis und strategischem Denken, um innovative Therapien zu entwickeln und zu vermarkten. In einem flexiblen und kollaborativen Umfeld haben Sie die Möglichkeit, an bedeutenden Projekten zu arbeiten, die das Leben von Patienten positiv beeinflussen. Wenn Sie leidenschaftlich an pharmazeutischer Innovation interessiert sind und eine Herausforderung suchen, könnte dies die perfekte Gelegenheit für Sie sein.

Leistungen

Flexible Arbeitszeiten

Home Office

Team-Events

Personalisierte Benefits

Coaching und Training

Qualifikationen

• 5+ Jahre Erfahrung in der pharmazeutischen Industrie erforderlich.
• Fähigkeit, regulatorische und klinische Strategien zu definieren.

Aufgaben

• Leitung komplexer Entwicklungsprojekte von der Konzeptphase bis zur Zulassung.
• Koordination externer Hersteller und Berater in Europa.

Kenntnisse

Projektmanagement

Regulatorische Strategien

Kommunikationsfähigkeiten

Kollaboration in interdisziplinären Teams

Ausbildung

Abschluss in Lebenswissenschaften

Tools

MS Project

SharePoint

Office365

Jobbeschreibung

(Senior) R&D Project Manager (f/m/d)

Pharma

Vienna

Are you passionate about advancing pharmaceutical innovation and making an impact on patients' lives? Our client - a financially stable, privately held pharmaceutical company with a start-up spirit - is looking for a hands-on and versatile R&D Project Manager (f/m/d). With a flat hierarchy and a collaborative culture, the company focuses on niche indications and develops both generics and innovative therapies, including biotech-enhanced drug-device combinations. In this role, you'll take ownership of end-to-end development projects - from early-stage concepts through preclinical and clinical phases to regulatory submission.

Your tasks

• Lead complex development projects end-to-end
• Define and execute regulatory, preclinical, and clinical strategies (EU & US focus)
• Coordinate external manufacturers, CROs, consultants, and suppliers across Europe
• Organize workshops, moderate expert discussions, and develop market-entry strategies
• Create and manage documentation (meeting minutes, regulatory files, scientific data)
• Bridge scientific, operational, and strategic aspects of product development
• Serve as the central point of contact between internal stakeholders and external collaborators
• Report to senior leadership and align with the company's strategic goals

Your qualifications

• Degree in life sciences (Pharmacy, Biology, Chemistry, Biotechnology, etc.)
• 5+ years of experience in the pharmaceutical industry - cross-disciplinary collaboration experience is a plus
• Experience across drug development phases: preclinical, clinical, registration
• Ability to read and apply guidelines with scientific rigor and business acumen
• Excellent communication skills, especially in cross-functional and multicultural environments
• Fluent in English (written & spoken); German is not required
• Proficient with MS Project, SharePoint, and Office365
• Hands-on, adaptable, and self-driven personality with a strategic mindset

The offer

• Remuneration: EUR 63,000 gross annual salary plus performance-based bonus with willingness to overpay
• A dynamic, flexible environment fostering professional and personal growth
• Benefits include flexible hours, home office, team events & personalized benefits
• Opportunities for coaching, training, and career development
• A visible role in a fast-moving, high-impact environment

If you are interested in this challenging position, please forward your CV to Viktoria Kaufmann quoting reference number E5173 to

smart bewerben

Weihburggasse 9 | A-1010 Wien
Tel. [phone]
www.eblinger.at