About the job

Clinical Project Manager

Come discover what our 25,000+ employees already know: work here matters everywhere. We’re
a growing and evolving biopharmaceutical industry leader, which means you’ll have endless
opportunities to work with experts around the world and build the career you’ve dreamed of.

As a part of the team, you’ll help us deliver results for a rewarding reason – we improve patients’
lives around the world. Because to us, a patient isn’t just a number, they’re our family, friends,
and neighbours.

Project Leadership And Delivery

Job responsibilities

 Manages a project as a project manager overseeing interdisciplinary clinical research

studies and ensures compliance with GCP, relevant SOP’s, and regulatory requirements.
 Acts as a primary liaison between the Company and the Customer to ensure timely study
launch, conduct, and closeout according to the Customer’s and the Company’s contractual
agreement.
 Lead project team to ensure quality, timelines and budget management.
 Accountable for the financial performance of each project.
 Coordinate activities and deliverables of all study conduct partners and proactively
identify and manage issues.
 Ensure studies are conducted in compliance with GCP, relevant SOP’s and regulatory
requirements.
 Accountable for all project deliverables for each project assigned.
Documentation And Reporting
 Responsible for quality and completeness of TMF for assigned projects.
 Accountable for maintenance of study information on a variety of databases and systems.
 Responsible for study management components of inspection readiness for all aspects of
the study conduct.
 Oversight for development and implementation of project plans.
 Plan, coordinate and present at internal and external meetings.
 Prepare project management reports for clients and management.
 Developing contingency planning and risk mitigation strategies to ensure successful
delivery of study goals.
Business Development

 Develops strong relationships with current clients to generate new and/or add-on
business for the future.
 May participate in bid defense meetings where presented as potential project manager.
Management

 May be required to line manage other project management team members and clinical
monitoring staff.
What We’re Looking For
 Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine,
Pharmacy, Nursing or equivalent combination of education and experience.
 Clinical research organization (CRO) and relevant therapeutic experience preferred.
Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory
requirements
 Strong organizational skills.
 Strong ability to manage time and work independently.
 Direct therapeutic area expertise.
 Ability to embrace new technologies.
 Excellent communication, presentation, interpersonal skills, both written and spoken.
 Ability to travel as necessary (approximately 25%).