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Senior Global Study Leader, Biopharmaceuticals

Местоположение Миссиссога, Онтарио, Канада Идентификатор вакансии R-102001 Дата публикации 03/15/2021

Are you passionate about leading clinical trials and drug development? 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.

About AstraZeneca:

AstraZeneca is a global, innovation-driven Biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s leading pharmaceutical companies.

 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.

AstraZeneca Canada:

Headquartered in Mississauga, Ontario, we’ve been recognized as one of Greater Toronto Area’s Top Employers for 7 straight years. Our collaborative work environment fosters knowledge-sharing, decision-making, and entrepreneurial thinking. Our employees have the opportunity to work across teams, functions, and even the globe. With a commitment to sustainability, we’re working towards making a meaningful impact where society needs it — health. We know the health of people, the planet and our business are interconnected, each impacting the others.

Our dynamic culture truly sets us apart. We support our people every day, focusing on three priorities: employee growth & development, health & wellbeing, and cultivating a vibrant, engaged and energized workplace. Through practical tools, resources, inspiring learning opportunities, and health and wellness support, we are helping our people thrive at work and beyond.

Our Biopharmaceuticals Research and Development Team:

Join the team unlocking the power of what science can do. We are working towards treating, preventing, modifying and even curing some of the world’s most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world.

Thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment. It’s a place to think differently – to find new ways of handling and treating diseases. We are trusted and empowered to explore.

What you’ll do:

  • Accountable for the operational planning and delivery of high priority and complex clinical studies within a program, or across programs that are deemed most critical to the business

  • Lead a cross-functional study team (core and extended), providing direction and guidance while ensuring effective partnership and teamwork to enable successful delivery of studies

  • Provide input to early study planning activities based on operational expertise

  • Lead and coordinate a team of experts in accordance with STOM and its roles, accountabilities and responsibilities framework (RACI) to ensure the clinical study progress as planned driving achievement of timelines, budget and quality standards

  • Contribute to vendor/ESP selection activities at the study level, including bid defense, and lead operational oversight

  • Assist the Director of Study Management with planning for upcoming clinical studies

  • Collaborate with other functions to establish strategies and identify common practices aimed at increasing efficiency of global study teams

  • Lead and facilitate communication across functions and provide guidance to study team members as needed

  • For outsourced studies, be the primary AZ point of contact for the CRO Study Manager to ensure study delivery, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study, following relevant AZ SOPs and guidelines (e.g. description of services and transfer of obligations)

  • Provide operational expertise into and hold accountability for the development of essential study level documents (i.e. Clinical Study Protocol (CSP) through to Clinical Study Report (CSR)

  • Ensure all external service providers (i.e. central laboratories, IXRS, ePRO, etc.) engaged are performing to contracted goals and timelines/budget and that adequate oversight is documented through planning & control activities

  • Develop and maintain relevant study plans including required input into study level quality and risk management planning with risk response strategies and clear issue resolution pathways

  • Oversee study level performance against agreed upon plans, timelines and key performance indicators (quality and operational) by using company tracking systems and project timelines, while communicating any risks to timelines and/or quality to CPT, along with proposed mitigations

  • Identify and report quality issues that have occurred and collaborate with all functions as necessary to overcome barriers and achieve desired outcomes

  • Oversee Trial Master File (TMF) completion including ensuring the TMF plan and Expected Document List are in place and that QC activities are performed on an ongoing basis

  • Ensure timely compliance with company-wide governance controls (e.g. Delegation of Authority, Sunshine Act, ACCORD attestations, Clinical Trial Transparency)

  • Responsible for study budget re-forecasting following initial budget estimate provided by the CPT and accountable for budget management through the study lifecycle

  • Ensure studies are inspection-ready at all times, according to ICH-GCP and AZ SOP and relevant policies/guidelines

  • Support professional development of team by providing regular feedback on individual performance

  • Provide guidance, training, expertise, mentoring and support to less experienced GSL colleagues

  • Leads non-drug project work such as SMO representative in process improvements and/or leading improvement projects as discussed and agreed upon with their manager

Essentials for the role:

  • University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research

  • Previous project management experience and training

  • At least 7 years of clinical trial experience

  • At least 3 years of experience in global study leadership and team leadership

  • Extensive knowledge of ICH-GCP guidelines and clinical research regulatory requirements and experience in all phases of clinical study delivery; start up, maintenance and close out.

  • Thorough understanding of the cross-functional clinical trial process e.g. Data flow

  • Strong strategic and critical thinking abilities with proven skillset to solve complex problems

  • Strong abilities in establishing and maintaining effective working relationships with strong conflict management skills

  • Demonstrated abilities in mentoring

  • Excellent communication and interpersonal skills

  • Ability to lead multiple challenging priorities

  • Experience in external provider oversight and management

Why AstraZeneca?

This is the place to make a meaningful impact – on patients’ lives and your personal growth. It’s both rewarding and inspiring, and it’s what keeps us motivated every day.

Great People want to Work with us! Find out why:

Are you interested in working at AZ, apply today!



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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