Associate Director, Evidence Project Management

At AstraZeneca we pride ourselves on crafting a collaborative culture that champions knowledge-sharing ambitious thinking and innovation ultimately providing employees with the opportunity to work across teams functions and even the globe.

Recognizing the importance of individualized flexibility our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office and BlueSky Hub in downtown Toronto are purposely designed with collaboration in mind providing space where teams can come together to strategize brainstorm and connect on key projects.

Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people the planet and our business are interconnected which is why were taking ambitious action to tackle some of the biggest challenges of our time from climate change to access to healthcare and disease prevention.

The Medical Evidence Delivery Team within Oncology Business Unit (OBU) is responsible for strategic planning and operational delivery of interventional and observational AstraZeneca sponsored studies (AZ studies) externally sponsored scientific research (ESR) and early access programs (EAP) in order to generate the evidence to build confidence in and provide access to AstraZeneca therapies for patients in need.

Associate Director Evidence Project Management (AD EPM) will lead the operational planning delivery oversight and budget management of company sponsored evidence studies and/or EAPs within the assigned therapeutic area (TA). This person is responsible for leading a cross-functional AstraZeneca (AZ) study team and supervising the CRO study team as well as for providing the teams with direction and guidance to enable successful study and/or EAP delivery. The AD EPM is the main liaison between the AZ and CRO teams and is accountable for the delivery of a study and/or EAP according to agreed upon timelines budget and quality standards by ensuring an effective partnership and teamwork within study team and external partners.
This person will also lead the study and/or EAP team in accordance with the clinical outsourcing model (i.e. EMPOWER early access principles) current clinical trial regulations (e.g. ICH GCP) AstraZeneca Standard Operating Procedures (AZ SOPs) AZ policies and standard processes and in line with AZ values and behaviours.

In addition they will support OBU Medical Evidences continuous improvement by developing expertise in a specific area of study delivery serving as a point of contact for standard process and contributing to the development and maintenance of guidance documents and training materials.
Associate Directors Evidence Project Management II are the group of most experienced AD EPMs who will serve their less experienced colleagues as mentors. They pose the ability to handle an increased complexity to lead departmental initiatives and to stretch up as needed.

Responsibilities:

• Partner with direct manager ensuring provision of expertise and operational input into the programs (e.g. IMAP ERT MARCO SDC CSP)

• Collaborate with Dir EPM /Sr Dir EPM and provide adequate input to enable effective CRO selection

• Work with externally managed/outsourced partners for studies planning and delivery

• Serve as the reference point for communication and escalation of issues

• Mentor coach and support the study team members.

• Lead a cross-functional study team in accordance with EMPOWER to ensure study progress as planned and driving achievement of breakthroughs.

• Be primary AZ point of contact for the CRO Project Manager to secure study delivery according to set criteria.

• Ensure the appropriate level of oversight of the CRO is maintained and documented throughout the study lifecycle in alignment with relevant AZ SOPs and guidelines (e.g. Sponsor Oversight Plan Description of Services)

• Co-ordinate/lead timely contributions of AZ core/extended members

• Collaborate with key partners cross-functionally and/or external partners to identify handle and resolve issues affecting study delivery

• Review protocol drafts and input operational perspectives/content into document and authoring team discussions

• Provide input into and/or quality review and hold accountability for the development of crucial study level documents (e.g. ICF study plans and guidelines) delegate responsibilities among the team as appropriate

• Ensure all required External Service Providers (e.g. CROs) are engaged at the study level (including execution of relevant vendors contracts) and are performing to contracted goals timelines and budget as well as adequate oversight is documented

• Responsible for study budget management through the study lifecycle and for providing budget progress updates to Dir EPM /Sr Dir EPM including any financial risks and mitigation plans (as part of the ongoing study change control process)

• Maintain/report accurate cost forecasts throughout study lead study spend within available budget & agreed tolerances

• Lead/be responsible for financial processes (POs invoicing cost reconciliation etc.) may delegate as appropriate

• Responsible for setup of the study cost tracker

• Monitor study risks throughout delivery and oversee team in the development/implementation of mitigations and contingencies

• Oversee study/EAP level performance against agreed upon plans achievements and key performance metrics EAP exit strategy

• Identify and report quality issues that have occurred within the study proactively communicate findings and corrective action plans (CAPA) to relevant collaborators

• Supervise periodic TMF QC and responsible for review of relevant sections/documents in accordance with SOP/Wiki

Specifically in the EAP space if assigned to in addition to the above:

• Lead program planning set up implementation and delivery of EAP in collaboration with local/regional/global medical and market access teams

• Participate in operational governance activities related to agreed CRO strategic and operational governance principles

• Perform vendor oversight to ensure EAP delivery to time cost and quality

• Collaborate with vendors to ensure the EAP operational aspects are effectively undertaken and that they have clear remits for delivery

• Manage resolution of program specific issues and partner concerns with internal and external team members

Requirements:

Essential:

• Bachelors degree required preferably in medical or biological science or equivalent by experience

• 3 years of experience in extensive pharmaceutical industry/CRO experience within clinical study/research project delivery drug development process and relevant guidelines for example GCP/ICH for a specific therapeutic and geographical area

• Project Management qualification or demonstration of project management skills including scope budget timeline resource management and use of associated tools

• Ability to effectively work with Clinical Research Organisations/External Providers

• Ability to mentor develop and educate staff

• Leadership promoting motivation and empowerment of others in order to accomplish individual team and organisational objectives

• Ability to look for and champion more efficient and effective methods/processes of delivering evidence studies focusing on key performance metrics around reliability efficiency cost and quality

• Consistent record in interacting widely and effectively within the company across regions functions and cultures

• Persuasive communicator in English with a proven track record to work collaboratively in a multi-cultural environment

Desirable:

• Experience and knowledge within compliance management of Early Access Program

• Advanced degree in medical or biological sciences or field associated with clinical research

• Experience of incorporating digital health and patent centric strategies into clinical studies

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AstraZenecais an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment assessment and selection process and may be requested by emailing .

Annual base salary for this position ranges from 131520.80 to 172621.05.

AstraZeneca is committed to providing fair and equitable compensation opportunities to all colleagues. Our compensation policies and practices have been designed to allow colleagues to progress through the salary range over time as they progress in their role. The range provided in this posting represents an offer pay range used in a majority of situations. The base pay offered will vary depending on multiple individualized factors including the candidates skills and experience job-related knowledge and other specific business and organizational some cases offers outside the range may also be considered to address unique circumstances.

In addition our permanent positions offer an annual Variable Pay Bonus/Short Term Incentive opportunity as well as eligibility to participate in our equity-based long-term incentive program (if applicable to role). Benefits offered for permanent roles include a competitive Flex Benefits & Retirement Savings Program 4 weeks paid vacation and annual Personal Days. Fixed Term Contract/Temporary positions (excluding students) are offered a Contract Benefits Program.

We are using AI as part of the recruitment process.

This advertisement relates to a current vacancy.

Required Experience:

Director