AZ currently require an interim Snr GSM for a remote based role on a 12-month contract.
Title
- Snr Global Study Manager
Location
- Remote
IR35 Status
- Inside
Duration
- 12 months
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.
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 delivery of early-phase global clinical studies within Oncology R&D from study set-up through maintenance, close-out and study archiving. The GSM works cross-functionally with partners to lead & deliver aspects of the clinical study.
Duties will include:
Lead/contribute to the preparation of study documents.
Maintaining and facilitating interactions with both internal and external functions such as CRO to ensure an efficient study delivery to time, cost and quality objective.
Contributing to the planning and conduct of internal and external meeting such as Investigator’s Meetings.
Ensure supply of investigations product and study materials
Ensure that all study documents in scope of GSM’s responsibilities 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 discipline associated with clinical research.
- 5+ years of industry experience in Early Phase study management
- 6+ years of industry experience within oncology (desirable)
- Extensive knowledge of GCP, clinical research regulatory requirements and demonstrated abilities in clinical study management processes and clinical/drug development.
- Demonstrated solid project management skills and knowledge of 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. An inclusive culture that champions diversity and teamwork. Always committed to lifelong learning, growth and development.
We'd love to hear from you if you have suitable experience by applying to the role
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.
- Owen Lavers
