Study Director

4 weeks ago

London, United Kingdom AstraZeneca Full time
Location – RemotenOutside IR35nDuration – 12 Months

Make a meaningful difference at AstraZenecanBring out the best in each other, and yourself, by working together as one.nWhen we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world .

​At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people’s exceptional skills with those of people from all over the globe.

The Director Study Leader, Early Oncology Clinical is responsible for delivering a single or several smaller development programs or leading multiple studies or single complex/novel studies such as platform, basket, etc. The exact accountabilities will differ depending on the exact nature of the clinical program so a high degree of flexibility and autonomy is required.

Responsibilities:

Provides expert clinical operational input into project or study level documents, for example clinical development plan, clinical study protocol, clinical study report, and may lead the delivery of study documentsnWith oversight from the Senior Director Clinical Programs, may lead and deliver differentiated and robust operational options for review at Investment Decision Governance interactionsnLeads the delivery of the clinical study program(s) or study(s) from concept to final CSR and through to study closure and archive to agreed budget, time, project standards, quality and scientific standardsnAccountable for overall study or program deliverables, maintaining oversight by close interaction with individual study leaders or leadership of the study team as appropriatenImplement agreed study level process and technology for Early Oncology clinical studiesnDevelops and manages effective risk management/mitigation plans to ensure timely delivery to quality, budget and time and escalate issues to stakeholders as appropriatenResponsible for planning and leading issue escalation and resolutionnProvide input to forecasting and management of study delivery costs, resource and timelinesnAccountable for the quality of study planning information into relevant planning systemsnGuide the study team in the development of outsourcing specifications and vendor selection

Essential Requirements:

Bachelor’s degree in related discipline, preferably in medical or biological sciencenAt least 10 years drug development experience demonstrated in a variety of rolesnAt least 5 years of experience in leading studies/programs in clinical developmentnComprehensive knowledge of the clinical and pharmaceutical drug development processnExtensive and proven experience in driving operational delivery to timelines, cost and qualitynProven experience leading delivery through internal and external organizations.nProject Management experience within the context of Clinical Drug DevelopmentnExperienced within matrix leadership

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, colour, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status.nAstraZeneca 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 authorization and employment eligibility verification requirements.

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