Clinical Project Leader – French Speaking

BioTalent Canada; Toronto; On-site; CAD 80,000 - 100,000; Full time

Job summary

A leading pharmaceutical company based in Toronto is seeking a Clinical Operations Study Lead to manage and oversee clinical trials. The role involves strategizing country-specific studies, managing budgets, and ensuring compliance with quality standards. Ideal candidates will have at least 3 years of clinical research experience and a relevant degree. The position also offers a great opportunity for career growth and engagement in a diverse work environment.

Benefits

Health and wellbeing benefits

Growth opportunities

Supportive team environment

Qualifications

• Minimum 3 years of experience in clinical research is mandatory.
• Experience in project management and site-coordination is preferred.
• Solid knowledge of clinical development process required.

Responsibilities

• Develop local study country strategy and lead activities.
• Ensure compliance with study planning and timelines.
• Manage the study budget during the course of the study.

Skills

Clinical research experience

Project management

Problem-solving

Data analytic skills

Fluent in English and French

Education

Bachelor’s degree in nursing, biochemistry or related natural science

Job description

Department : Project Management CSU Canada

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.

COSCL I is the country level operational lead in clinical studies. He / she owns, and is accountable for, the strategic planning, management and performance of their assigned clinical trials, for his / her country(ies), from country allocation until study closure at the Clinical Study Unit (CSU) level including study country timelines, study country budget, and study conduct in accordance with Sanofi Standard Operating Procedures (SOPs) and / or Quality Documents (QD)s and ICH / GCP and regulatory guidelines & directives. The COSCL I is the key strategic interface, at country level, with internal and external stakeholders to manage operational processes to accelerate trial conduct. Key interfaces for COSCL are :

• Globally : Clinical Operations Study Lead (COSL), Data Management, Vendor Management, Study Medical Manager, Clinical Supply Chain Study Manager, Patient Recruitment and Retention Lead and other Core Study Team members / transversal roles
• Locally : Clinical Research Associate (CRA), Clinical Project Assistant (CPA) Medical Advisor (MDA), Site Engagement Lead (SEL), Start-Up Strategy Manager (SUSM), Medical Science Liaisons (MSL) and other relevant roles.

COSCL I represents their CSU at the Core Study Team meetings. COSCL I reports to CSU Team Lead or CSU Head in their given CSU country, while working closely functionally with COSL for study topics. While the COSCL may consult COSL or escalate on operational issues that could affect study costs, speed or quality in the CSU, the COSCL is fully accountable to deliver the study as planned in their CSU level.

We are an innovative global healthcare company with one purpose : to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main responsibilities

Set up local study country strategy and lead country start up activities :

• Develop and initiate early recruitment and retention strategy and associated materials at local level in collaboration with respective colleagues,
• Identify most successful site mapping and set up site engagement strategy aligning with SEL and MDA,
• Organize the local kick off meeting and lead set-up activities to ensure progress according to study timelines with strategic planning.

Lead local study management at CSU on execution of clinical studies according to global and local study plan :

• Fully own the local level performance of the study, ensuring the study is conducted in compliance with planning and agreed timelines.
• Accounts for the set-up, completion, and adaptations of project management tools at country level (CTMS, Control room…)
• Drive performance of the study with risk assessment and mitigation strategies, manage sites engagement aligning with SEL (Site Engagement Lead) and MDA (Medical Advisor) regarding site motivation and provide support to site staff and monitoring team in the conduct of clinical trials. COSCL is the member of Core Study Team meetings representing their CSU.
• In case of discrepancies / gaps on performance, COSCL should proactively escalate, propose and discuss mitigation and contingency strategy with COSL.

Owns Study Budget at country / cluster level and ensures optimization and appropriate management of the financial resources :

• Collaborate with Start-Up Strategy Manager (SUSM) for preparation of Local Study Budget Form (LSBF) ensuring cost optimization and appropriate projection at the beginning of the study.
• Manages and maintains Country Study Budget during course of study, ensures timely escalation of issues / risks related to the country budget and initiate LSBF updates.

Lead effective communication between all local parties involved in the study to align common goals and define best strategies :

• Be the main link to the local monitoring team in the management of studies.
• Collaborate with Vendor Functional Line Managers (FLM) to drive quality and study KPIs, Plan / participate in study site engagement activities (i.e. Recruitment Booster calls),
• Work closely and proactively with MDAs / SELs early on to drive the country strategy, coordinate local study team meeting,
• Establish collaboration with GBU Medical Affairs regarding trial conduct and medico-marketing activities.
• Proactively escalate any resource related risks / issues to CSU management and propose and discuss mitigation strategy at CSU level to ensure appropriate resource allocation and optimization for the study.

Maintain Quality and Compliance :

• Responsible for data quality, patients’ safety and maintain compliance to study metrics for his / her country(ies).
• Ensure appropriate quality for data collection and queries resolution.
• Ensure CRA Study Training according to Study Training metrics through FLMs,
• Collaborate with QL on audit and inspection related activities,
• Ensure PAI readiness within CTMS, TMF and other systems.

About you

Requirements :

• Bachelor’s (or higher) degree in nursing, biochemistry or related natural science
• 3 years minimum experience in clinical research is mandatory, preferably in combination with experience in project management and certain time as field monitor or site-coordinator.
• Solid knowledge of clinical development process and relevant therapeutic / disease area(s)
• 3 years minimum hands-on experience in Project Management, PMP certification is nice to have
• Problem-solving and risk-management skills in a clinical study environment
• Data analytic skills and use of digital tools, platforms and systems
• Interpersonal skills with ability to create and foster trustful relationships with several internal and external stakeholders
• Languages : Fluent in English and French.
• 10% travel (in-country travel)

Why Choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs

This position is for a current vacant role that we are actively hiring for.

Sanofi is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. We welcome and encourage applications from all qualified applicants. Accommodations for persons with disabilities required during the recruitment process are available upon request.

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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Join Sanofi and step into a new era of science – where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Watch ‘One day at Sanofi’ and check out our Diversity Equity and Inclusion initiatives at sanofi.com

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