Social network you want to login/join with:

Title

- Global Study Manager

Location

- Remote

IR35 Status

- Inside

Duration

- 12 months

Make a more meaningful impact on 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 our patients and shaping the patient ecosystem.

If your passion is science and you want to be part of a team that makes a bigger impact on patients’ lives, then there’s no better place to be.

The Global Study Manager will work closely with the study operations team and Study Leader, who is the overall accountable for the delivery of the study. The GSM supports the delivery of early-phase global clinical studies within Oncology R&D from study setup through maintenance, close-out, and study archiving. The GSM works cross-functionally with partners to lead and deliver aspects of the clinical study.

Responsibilities include:

1. Leading and contributing to the preparation of study documents.
2. Maintaining and facilitating interactions with internal and external functions such as CROs to ensure efficient study delivery within time, cost, and quality objectives.
3. Contributing to the planning and conduct of internal and external meetings, such as Investigator’s Meetings.
4. Ensuring the supply of investigation products and study materials.
5. Ensuring all study documents within the GSM’s scope are complete and verified for quality in the Trial Master File.

Essential Qualifications and Experience:

• University degree (or equivalent), preferably in medical or biological sciences or a discipline related to clinical research.
• 5+ years of industry experience in early-phase study management.
• 5+ years of industry experience within oncology (desirable).
• Extensive knowledge of GCP, clinical research regulatory requirements, and demonstrated abilities in clinical study management processes and drug development.
• Proven project management skills and familiarity with relevant tools.

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. We foster an inclusive culture that champions diversity and teamwork. We are committed to lifelong learning, growth, and development.

We’d love to hear from you if you have the suitable experience. Apply to the role today!