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Study Start-Up Managers EU CTR

地点 劍橋, 英格兰, 英国 于克勒, Bruxelles-Capitale, 比利时 布拉迪斯拉发, Bratislava, 斯洛伐克 布达佩斯, Budapest, 匈牙利 斯德哥尔摩, Stockholm County, 瑞典 布加勒斯特, București, 羅馬尼亞 布拉格, Hlavní město Praha, 捷克 Milan, Lombardia, 意大利 Cambridge, Comunidad de Madrid, 西班牙 汉堡, Free and Hanseatic City of Hamburg, 德国 Cambridge, 索菲亞州, 保加利亚 职位 ID R-144664 发布日期 08/03/2022

Study Start-Up Managers EU CTR

Locations: Across Europe where we have an Site Management & Monitoring (SMM) presence

Competitive salary and benefits

Make a more meaningful impact to patients’ lives around the globe

Here you’ll have the opportunity to make a meaningful difference to patients’ lives. With science at its heart, this is the place where breakthroughs born in the lab become transformative medicines – for the world’s most complex diseases. Answer unmet medical needs by pioneering the next wave of science, focusing on outcomes and shaping the patient ecosystem.

Join the team that follows the science unlike anywhere else. This is the place for curious minds. Dig deep into the biology of complex disease and uncover breakthroughs.

This role - internally known as a EU CTR Part 2 Coordinator (P2C) - is responsible for project management and coordination of the EU CTR Part 2 submissions together with global regulatory, global study team and local study teams from the participating countries in compliance with the EU CTR requirements, AZ procedures, documents, local and international guidelines and relevant regulations. The creation of this team is hugely exciting and these positions are pivotal to the success of the program. You will receive specific training during the onboarding process. These roles would suit candidates with Local Study Associate Director (Manager) level experience.

Typical accountabilities:

Management, coordination and collation of Part 2 packages

  • Attend the global submission planning kick off meeting(s)
  • Agree on timeline planning for submission with global and local teams.
  • Ensure local teams are fully aware of submission timelines to allow robust SQV’s / site selection visits to occur with EU/EEA sites
  • Ensure global documents are provided to local teams in time for Part 2 package preparation. Hold global team accountable for delivery.
  • Collate Part 2 submission Table of Content (ToC) and corresponding part 2 documents completed by local study associate directors.
  • Reach out to the countries to ensure ToC reflects the country submission documents and meets the EU CTR requirements
  • Check completeness, not content, of Part 2 submission packages (downloaded documents) with ToC
  • Hold EU/EEA local teams accountable to the delivery of the part 2 package to the agreed timelines

Provide support to local teams

  • EU CTR specific questions
  • Questions on document content
  • Provide support and coordinate Part 2 RFI responses
  • Ensure agreement between local teams and global teams on translations as required (CTIS fields, CSP synopsis, cover letter etc.)

Collation of Part 2 substantial modifications, non-substantial modifications and notifications

  • Handling of Part 2 substantial and non-substantial modification requests and notifications from countries – coordinate submissions together with any Part 1 substantial modification

Essential criteria

  • Fully understand the EU CTR regulation, AZ regulatory and clinical trial start up process
  • Understands AZ study operation model on global and local level
  • Bachelor degree in related discipline, preferably in life science, or equivalent qualification and experience
  • Good knowledge of international guidelines ICH-GCP as well as relevant local regulations, basic knowledge of GMP/GDP
  • Basic understanding of drug development process
  • Good collaboration and interpersonal skills
  • Excellent verbal and written communication skills
  • Excellent attention to details.
  • Excellent understanding of Clinical Study Management and study start-up
  • Good negotiation skills
  • Good ability to learn and to adapt to work with IT systems.

Desirable criteria

  • Integrity and high ethical standards
  • Good analytical and problem-solving skills
  • Basic change management skills
  • Good intercultural awareness
  • Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time
  • Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines
  • Team oriented and flexible; ability to respond quickly to shifting demands and opportunities

Why AstraZeneca

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

So, what’s next?

This role is open from (Day, Month, Year). We will continuously review candidates on an ongoing basis, so there’s a chance this role will close shortly, should we fill all of the positions.

Where can I find out more?

Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/

Follow AstraZeneca on Facebook https://www.facebook.com/astrazenecacareers/

Follow AstraZeneca on Instagram https://www.instagram.com/astrazeneca_careers/?hl=en



AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

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