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Clinical Operation Manager Jobs in Quebec (NOW HIRING)

Manager, Clinical Data Management

Montreal, QC ยท On-site

CA$99K - CA$166K/yr

Ensure operational efficiency and excellence by leading and/or assisting in the creation and documentation of new or revised department procedures. * Recommend appropriate departmental objectives ...

We are seeking Assistant Clinical Nurse Managers to support the clinical and operational management of care units while ensuring the delivery of quality nursing care. Under the authority of the unit ...

Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. * Escalates to the project manager any risks to clinical trial ...

... Clinical, Biospecimen, Imaging and Genetic (C-BIG) repository research initiatives focused on ... Contribute to reports, operational analyses, presentations, and metrics used to support strategic ...

... Clinical, Biospecimen, Imaging and Genetic (C-BIG) repository research initiatives focused on ... Contribute to reports, operational analyses, presentations, and metrics used to support strategic ...

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Clinical Operation Manager information

What are some common challenges Clinical Operation Managers face when coordinating multi-site clinical trials?

Clinical Operation Managers often encounter challenges such as ensuring consistent protocol adherence across all sites, managing communication among geographically dispersed teams, and maintaining timelines despite unexpected delays. They must also address regulatory differences between sites and troubleshoot issues related to patient recruitment and data collection. Success in this role requires strong organizational skills, adaptability, and effective collaboration with investigators, coordinators, and regulatory personnel.

What are the key skills and qualifications needed to thrive as a Clinical Operation Manager, and why are they important?

To thrive as a Clinical Operation Manager, you need expertise in clinical project management, regulatory compliance, and a background in healthcare or life sciences, often supported by a relevant degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as PMP or Six Sigma are commonly required. Strong leadership, problem-solving abilities, and excellent communication skills set top performers apart in this role. These competencies are essential for ensuring efficient clinical operations, maintaining regulatory standards, and leading teams to deliver successful trial outcomes.

What are Clinical Operation Managers?

Clinical Operation Managers are professionals responsible for overseeing the daily operations of clinical research sites, medical facilities, or departments. They ensure that clinical trials or healthcare services are conducted efficiently, comply with regulations, and meet quality standards. Their duties often include supervising staff, managing budgets, implementing policies, and coordinating between various teams. Clinical Operation Managers play a crucial role in ensuring that patient care and research activities run smoothly and effectively.

What is the difference between Clinical Operation Manager vs Clinical Research Coordinator?

AspectClinical Operation ManagerClinical Research Coordinator
CredentialsBachelor's degree in health sciences, life sciences, or related field; often with project management certificationsBachelor's degree in health sciences, nursing, or related field; often with research-specific training
Work EnvironmentOversees multiple clinical trials, manages teams, and ensures compliance at a departmental levelCoordinates daily activities of clinical trials, interacts directly with participants and investigators
Employer & IndustryPharmaceutical companies, biotech firms, hospitals, research institutionsResearch sites, hospitals, academic institutions, contract research organizations

The Clinical Operation Manager focuses on overseeing clinical trial operations, managing teams, and ensuring compliance across projects. In contrast, the Clinical Research Coordinator handles the day-to-day activities of specific trials, working closely with participants and investigators. Both roles require relevant healthcare or science credentials, but their scope and responsibilities differ significantly.

What job categories do people searching Clinical Operation Manager jobs in Quebec look for? The top searched job categories for Clinical Operation Manager jobs in Quebec are:
Infographic showing various Clinical Operation Manager job openings in Quebec as of July 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 80% In-person, 6% Hybrid, and 14% Remote job distribution.

Associate Director, Operations - Clinical Assessment Technologies (CAT) - US/Canada - Remote

Worldwide Clinical Trials

Quebec, QC โ€ข Remote

Full-time

Re-posted 7 days ago


Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What theBusiness Development OperationsDepartment does at WorldwideBusiness

Development Operations is a team of highly experiencedBusiness Development professionalswho drive significant bookings targets and supportWorldwide'sstrategic position in a competitive market through a culture of collaboration and innovation.

This tenured team supports a strong portfolio of existing business as well asbeing responsibleforthe continued significant growth ofWorldwide'sfuture pipeline and sponsors.The team isaccountable for overall sales performance, the profitable achievement of sales goals, and for aligningsales objectiveswith theWorldwide'stherapeutic and commercial strategies.

What you willdo

  • Identifyoperational needs for upcoming projects, track and review current assignments for CAT Operations staff

  • Resource CAT study projects as Resource Manager

  • Engage as Subject Matter Expert (SME) for CAT Operations activities

  • Provide operational oversight for designated CAT study projects

  • Engage in and coordinate resourcing activities for all CAT awarded projects

  • Identifytraining and skills gaps among staff; coordinate andassistwith learning opportunities to enhance operations staff knowledge and skills of industry related regulations, processes, materials, and guidelines

  • Activelyidentifyand engage in process improvement activities

  • Participate in QMD reviews and new QMD development

  • Author, collaborate, and review QMD documents and guidance documents

  • Coordinate and manage CAT Operations team meetings

  • Active engagement and oversight of study risk assessments, as they relate to operational activities

  • Work with department leaders to ensure alignment among CAT operational and clinical services

  • Lead and/or contribute to departmental initiatives that aim to implement polices, methods, techniques to contribute to existing service areas and department growth

  • Accountable for oversight of CAT study deliverables from Launch process to study close out

  • Assistand collaborate with Operations staff, Project Management, Contracts on vendor and study budget development, scope of work revisions,trackingand compliance

  • Assistin vendor management related concerns, including involvement with escalations, Vendor Management and Quality Assurance meetings

  • Review and assess ongoing budgetutilizationand revenue recognition with Operations Managers to ensure projects are meeting financial targets

  • Manage internal CAT operations meetings and other trial-specific meetings, as appropriate

  • Significant contributor to multiple strategic departmental, sponsor-relatedand cross-functional initiatives

  • Participate in business development activities including; but not limited to proposals input, capabilities, and biddefensemeetings

  • Apply thorough knowledge of industry regulations and guidelines to ensure operational compliance during clinical trial conduct

What you will bring to the role

  • Exceptional organizational skills, detail- and service-oriented, with excellent management / supervision skills

  • Excellent understanding of best business practices with respect to clinical trial operations and rater reliability processes

  • Knowledge and capabilities of our technology vendors and their abilities (skill)Excels in planning, managing, monitoring, and critiquing skills

  • Excellent at meeting timelines consistently and being able to effectively work under pressure

  • Continuously open to constructive, developmental feedback

  • Exceptional interpersonal skills in a fast-paced, deadline oriented, and changing environment

  • Excellent ability to proactivelyidentifyand escalate potential project issues toappropriate CATand WCT staff

  • Basic knowledge of statistics and finance practices

Your experience

  • Must have a minimum of a bachelor's degree, preferably with anMaster'sdegree (life sciences,MBAand/or PMP certification).

  • Strong leadership,managementand interpersonal skills

  • Strong planning and organizational skills

  • At least 7+ years clinical trial experience with at least 4 years' experience in global clinical trials

  • Preferred at least 5+ years of experience managing team members or project management experience

  • Hands on experience in day-to-day management of all aspects of global clinical trialsrequired

  • Prior experience in psychiatry / CNS therapeutic areas is a plus

  • The ideal candidatepossessesknowledge and appreciation of all stages of clinical drug development. Effective leadership skills and a proven ability to build and fosterhigh performanceteam productivity and cohesiveness isrequired. This position requires strong knowledge of monitoring practices,demonstratedknowledge / competence in the application of CFRs, GCPs and ICH guidelines

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):


United States of America - $112,000.00 - $223,000.00


The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.