Clinical Agreement Manager (12 Month Contract)
AstraZenecaCanada - mississaugaUpdate time: March 3,2021
Job Description

Do you have expertise in and passion for delivering clinical studies? Would you like to apply your expertise to help patients in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you!

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 five 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 our head office and internal and external meetings green.

Our dynamic culture truly sets us apart. Thrive@AZ, our platform to best support our people, focuses 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 Oncology Research and Development Team

Our pioneering approach is identifying and treating patients earlier, focusing on early stage cancer trials and listening and evolving based on their needs. As a team we are deeply committed to transforming the lives of patients living with cancer – with the ultimate aim of eliminating cancer as a cause of death.

What you’ll do

  • Manage the clinical study agreements drafting and negotiation process and ensure ethical, fair and compliant practices are followed when developing, negotiating and executing clinical trial agreements

  • Assists in and/or direct the development of terms and conditions, providing specialized support to global study leads in the planning, execution and control of contracts

  • Responsible for the negotiations, finalization and execution of Clinical Study Agreements and  Confidentiality Agreements

  • Manage and report the status of all study agreements, issues and communications with both internal and external sources.

  • Manage and resolve requested changes from institutions, suppliers, CRO related to Agreements, and from the site Ethics boards related to Informed Consent Form.

  • Collaborate with Legal Department and external Legal Counsel as necessary to identify solutions related to contract finalization

  • Assures coordination of outsourced contract activities and become the main point of contact for escalation

  • Collaborate with CRO contracts team to enhance and streamline contract process

  • Determine potential needs for contract amendments and manage amendment execution

  • Assure that contractual terms and provisions are in compliance with corporate process, systems, and strategies

  • Assume responsibilities for all aspects of document tracking and management

  • Consultation with Compliance to seek approval on specific issues to finalize agreements and Patient Informed Consent

  • Ensure that the final contract documents and study budgets are consistent with agreements reached during the negotiation process

  • Attend and engage in scheduled project team meetings as required.

  • Support internal and external audits

  • Participate in operational teams to deliver standardized and improved processes, procedures and tools

  • Provide solutions to unique challenges and use these as a precedent for future decisions

Essentials for the role:

  • Bachelor’s degree in life sciences, business or law

  • Post graduate training in contracts administration or work experience as a paralegal in pharmaceutical or health care industry an asset

  • Strong leadership, interpersonal, negotiation, communication and time management skills

  • A strong understanding of the drug development process in the pharmaceutical or healthcare industry and a solid understanding of project management principles and methodology

  • Strong oral, written and organizational skills, with experience in making decisions and developing solutions

  • Strong contract language drafting and negotiation skills with exceptional attention to detail

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!

Date Posted

02-Mar-2021

Closing Date

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 authorization and employment eligibility verification requirements.

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