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- Aufgaben: Manage pivotal programs and studies in Plasma-derived Therapy to ensure product quality.
- Arbeitgeber: Join Takeda, a leading biopharmaceutical company committed to better health globally.
- Mitarbeitervorteile: Enjoy hybrid work options, flexible hours, and extensive health and wellness offerings.
- Warum dieser Job: Be part of a dynamic team shaping healthcare with innovative therapies and a supportive culture.
- Gewünschte Qualifikationen: Relevant experience in medical affairs or research management is essential.
- Andere Informationen: Position based in Vienna, Austria, starting April 1, 2025.
Das voraussichtliche Gehalt liegt zwischen 60000 - 84000 € pro Jahr.
Your Role: Global Evidence Generation Operations Manager
In this key role within the Plasma-derived Therapy (PDT) Global Medical Affairs team, you will manage pivotal programs and studies to ensure product quality and innovation throughout their lifecycle.
About Us
At Takeda, we are shaping the future of healthcare with an unwavering commitment to creating better health and a brighter future for people worldwide. As a values-driven, research-oriented biopharmaceutical leader headquartered in Japan, Takeda has a strong footprint in Austria across the entire pharmaceutical value chain: from research and development to plasma collection, manufacturing, and distribution. With over 4,500 employees in Austria, our Vienna and Linz locations play a crucial role in delivering high-quality plasma-derived therapies and innovative medicines to patients globally.
We pride ourselves on being a certified Top Employer and a family-friendly company, fostering a healthy work-life balance, offering an inclusive workplace, and providing opportunities for professional growth.
Location: Vienna, Austria
Start Date: April 1, 2025
Working Hours: Full-time, 38 hours (all-in)
Your Responsibilities:
- Oversee Investigator Initiated Research (IIR), Externally Sponsored Collaborative Research (CCR), and Medical Affairs Company Sponsored Studies (MACS) within the PDT portfolio.
- Manage the end-to-end lifecycle of research projects, including study initiation, tracking, closeout, reporting, and operational aspects like finance, contracts, and drug supply coordination.
- Ensure studies are conducted in compliance with all applicable internal policies, SOPs, and external regulatory requirements.
- Act as the operational lead, collaborating with internal cross-functional global and local teams as well as external investigators.
- Support Evidence Generation team initiatives, such as Integrated Evidence Plan development, process improvements, and SOP updates.
Why Join Us?
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At Takeda, we offer a dynamic and inclusive workplace with a wide range of benefits designed to support your professional and personal growth:
- Work Environment: Certified family-friendly workplace, hybrid working options, and flexible working hours.
- Development Opportunities: Comprehensive training and development programs, mentoring, and job rotations in Austria and internationally.
- Recognition & Networks: Employee recommendation and recognition programs; participation in various network groups (e.g., Diversity, Equity & Inclusion, Sustainability).
- Health & Wellbeing: Extensive health and fitness offerings, free vaccinations, psychological counseling.
- Family Support: Bilingual corporate kindergarten and childcare options.
- Convenience: On-site restaurant with subsidized meals, excellent public transport connections, in-house fitness and wellness center in Vienna.
Join our mission to deliver better health to people worldwide!
Apply now and be a part of Takeda\’s journey.
Global Evidence Generation Operations Manager (m/w/d) Arbeitgeber: RIS Shire
Kontaktperson:
RIS Shire HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Global Evidence Generation Operations Manager (m/w/d)
✨Tip Number 1
Familiarize yourself with the specific regulations and compliance standards relevant to the biopharmaceutical industry. Understanding these will not only help you in interviews but also demonstrate your commitment to quality and safety in research operations.
✨Tip Number 2
Network with professionals in the field of medical affairs and evidence generation. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in the sector.
✨Tip Number 3
Highlight your experience in managing research projects, especially those that involve cross-functional teams. Be prepared to discuss specific examples of how you've successfully led projects from initiation to closeout.
✨Tip Number 4
Showcase your ability to improve processes and implement SOP updates. Think of instances where you've contributed to operational efficiencies and be ready to share these insights during discussions.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Global Evidence Generation Operations Manager (m/w/d)
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Global Evidence Generation Operations Manager position. Highlight key responsibilities and required skills that align with your experience.
Tailor Your CV: Customize your CV to reflect relevant experiences in managing research projects, compliance with regulatory requirements, and collaboration with cross-functional teams. Use specific examples that demonstrate your expertise in these areas.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for the biopharmaceutical industry and Takeda's mission. Mention how your values align with those of the company.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any grammatical errors or typos. A polished application reflects your attention to detail and professionalism.
Wie du dich auf ein Vorstellungsgespräch bei RIS Shire vorbereitest
✨Understand the Role
Make sure you have a clear understanding of the responsibilities of a Global Evidence Generation Operations Manager. Familiarize yourself with Investigator Initiated Research (IIR), Externally Sponsored Collaborative Research (CCR), and Medical Affairs Company Sponsored Studies (MACS) to demonstrate your knowledge during the interview.
✨Showcase Your Project Management Skills
Be prepared to discuss your experience in managing research projects from initiation to closeout. Highlight specific examples where you successfully coordinated operational aspects like finance, contracts, and drug supply coordination.
✨Emphasize Compliance Knowledge
Since compliance is crucial in this role, be ready to talk about your understanding of internal policies, SOPs, and external regulatory requirements. Share any relevant experiences that showcase your ability to ensure studies are conducted in accordance with these standards.
✨Highlight Collaboration Experience
This position requires collaboration with cross-functional teams and external investigators. Prepare examples of how you've effectively worked with diverse teams in the past, focusing on your communication skills and ability to foster teamwork.
