Job Description

Location: Mississauga, Ontario (Hybrid 3 days/week in office)

AstraZeneca Canada:

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation \xe2\x80\x93 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 fito 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 we\xe2\x80\x99re taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention.

Our Oncology Research and Development Team:

Oncology is driven by speed. Here you will be backed by leadership and empowered at every level to prioritize and make bold moves. Our pioneering approach is identifying and treating patients earlier, focusing on early-stage cancer trials and listening and evolving based on their needs.

Join a dedicated Oncology team that\xe2\x80\x99s growing fast and building a strong track record of success.

What you\'ll do:

Our data management team supports our global clinical studies from study start-up, to study close-out. The Associate Director, Study Data Manager (ADSDM) works with various study leaders building positive relationships across cross-functional teams to bring data integrity and ensure data quality of AstraZeneca\'s global late phase studies.

As a core member of the study team, the ADSDM is responsible for the overall quality and integrity of the clinical database, working positively with global study teams to ensure that AstraZeneca\xe2\x80\x99s Clinical Data is collected, managed, documented and reported clearly, accurately, and securely based on the study\xe2\x80\x99s protocol and to the highest scientific industry standards.

Accountabilities:

Coordinate the Clinical Data management deliverables on assigned studies depending on the relevant model and DM Vendor. Takes accountability and serves as the first line of contact at the study level.

Demonstrates leadership and operational knowledge in the planning and delivery of CDM deliverables at a study level potentially under mentorship from a Principle Clinical Project Data Manager.

Communicates and collaborates effectively with all study level team members. Primary point of contact for DM vendor and provides guidance and supervision to Lead Data Manager/DM Team Lead working on the study (CRO or in-house).

Oversight of the day to day operational aspects of CDM for assigned studies; Responsible to identify risks and collaborate with the DM Vendor to mitigate the risk.

Understands therapeutic area, indication or program specific data capture standards and AZ standards.

Provide input into CDM related activities associated with regulatory inspections/audits for assigned studies.

May provide input to the selection and use of software systems, devices and vendors.

Responsible for compliance to Trial Master File requirements relating to DM Vendor

Support Senior Leaders to oversee CDM Vendor performance, depending on relevant model. Review, assess and manage DM Vendor delivery against KPIs, budget and overall performance. Oversees vendor timelines and milestone deliverables for the assigned studies. Ensures DM Vendor billing is accurate and gives recommendations for payment of invoices.

Drive adherence to AZ CDM standards and processes for data quality and consistency of data capturing for assigned studies.

Maintain an awareness of the external and internal models in order to participate in change initiatives and continuous improvement activities related to CDM operating models.

Demonstrates willingness to take on ad hoc activities consistent with current or experience in support of CDM.

Mentoring junior Clinical Data management colleagues

Essentials:

Education: Minimum of a BSc in life sciences or related subject, pharmacy nursing or equivalent degree

Strong Data Management experience in the Biotech/Pharma/CRO industry

Demonstrated current understanding of GCP and regulatory requirements as they relate to data management systems and activities

Demonstrated current understanding of Good Clinical Data Management Practices (GCDMP)

Experience of clinical databases, different clinical data management systems and electronic data capture (EDC)

Demonstrate understanding and experience in query management process and reconciliation activities

Strong communication and interpersonal skills

Ability to work independently without close supervision

Excellent written and verbal communication skills

Effective problem and conflict solving skills

Ability to work in a global team environment

High attention to detail and accuracy

Desirable:

Certified Clinical Data Manager (CCDM) via the Society of Clinical Data Management

Demonstrated knowledge of clinical and pharmaceutical drug development process

State of the art understanding of database structures, data standards (CDISC) and practices as they apply to CRF design, database development, data handling and reporting

Knowledge of SQL, 4GL, VBA or R software

Demonstrated understanding of clinical data system design / development / validation and system interoperability.

Excellent understanding and demonstration of the AZ values and behaviors

Demonstrated professionalism, diplomacy, mutual respect and ability to manage and value diversity and cultural differences while promoting productivity through encouragement

Excellent organizational and analytical skills

Demonstrated ability to work effectively with external partners

Ability to interact effectively with all levels of management

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

Are you interested in working at AZ, apply today!

AstraZeneca is 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 .

Date Posted 17-Jul-2023

Closing Date 24-Jul-2023

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.

AstraZeneca