Clinical Trial Manager II

The Clinical Trial Manager II (CTM II), Dermatology & Rheumatology is responsible for the operational management and oversight of the clinical investigative sites as well as the clinical monitoring deliverables of clinical trials. This includes but is not limited to clinical research associate (CRA) training, identification of quality issues related to site performance and clinical monitoring activities, establishing action plans to address any concerns, as well as ensuring timelines are met. This Role Will Be Perfect For You If You enjoy working with a Canadian-owned mid-sized CRO where you can build professional relationships with your colleagues at all levels You bring previous experience in managing the clinical monitoring portion of clinical projects Dermatology is a therapeutic area you enjoy or want to learn more about RESPONSIBILITIES Ensures that clinical monitoring activities are performed to the Sponsor’s satisfaction, ensuring timely quality deliverables and in accordance with applicable standard operating procedures (SOPs), regulations, good clinical practices and study-specific requirements; Identifies quality issues and trends related to site performance and clinical monitoring activities through project meetings, site communications, site visit reports and follow-up letters, quality control visits, and quality assurance audit findings. Summarizes findings and establishes action plans to bring corrective actions; Serves as a point of contact for CRAs and Lead CRAs for assigned projects; Provides mentoring/oversight of CRAs and Lead CRAs; Performs site visit report review for assigned projects and tracks site visit report metrics to ensure compliance; Contributes to the development of the Clinical Monitoring Plan; Prepares and conducts project-specific training for the CRAs; Develops the annotated site visit reports and monitoring tools such as source data verification worksheets; Conducts quality control visits with CRAs; Coordinates and leads CRA meetings; Performs co-monitoring visits with CRAs; May be involved in business development activities (client meetings, proposal defense meetings, requests for proposals (RFPs) requests for information (RFIs)). Requirements IDEAL PROFILE Education B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience; Experience At least 8 years of clinical research experience including prior monitoring experience and at least 2 years of experience acting in a Lead CRA or Clinical Team Leader role in the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry; Knowledge And Skills Strong knowledge of ICH/GCP standards and applicable regulatory requirements; Excellent mastery of Microsoft Office suite (Word, Excel, Power Point); Ability to work in a fast-paced evolving environment and establish good relationships with colleagues, sites and sponsors; Excellent leadership, organizational, time management and multi-tasking skills; Excellent judgement and problem-solving skills; Occasional travel (up to 10% of the time), including some travel outside of the country once possible; Fluent in English (excellent oral and written), French is an asset; Experience in a CRO and in dermatology an asset.

The Clinical Trial Manager II is responsible for the operational management and oversight of clinical investigative sites and monitoring deliverables. This includes training CRAs, identifying quality issues, and ensuring study timelines and regulatory requirements are met.

Candidates need a B.Sc. in a relevant field and at least 8 years of clinical research experience, including 2 years as a Lead CRA or Clinical Team Leader. Strong knowledge of ICH/GCP standards and proficiency in Microsoft Office are required.

• Problem solvingPreferred
• LeadershipPreferred
• Microsoft OfficePreferred
• Project managementPreferred

Identified from the job description. Confirm important requirements above.

• Clinical Monitoring
• CRA Training
• Site Management
• ICH/GCP Standards
• Project Management
• Quality Control
• Clinical Trial Oversight
• Microsoft Office
• Leadership
• Problem Solving
• Dermatology
• Rheumatology
• Regulatory Compliance
• Mentoring
• Source Data Verification
• Clinical Research

• Healthcare
• Science & Research
• Management & Leadership
• Consulting

Minimum education

Bachelor’s degree

Minimum experience

5+ years

Apply by

Sep 23, 2026

Posting language

English

Working hours

40 hours per week

Seniority

Mid-Senior level

Application method

Direct apply is available