Senior Clinical Data Manager

Warman O'Brien; Boucherville; Remote; CAD 80,000 - 100,000; Full time

Job summary

A leading global CRO is hiring a Senior Clinical Data Manager for their team. This pivotal role involves overseeing data management projects, ensuring quality control in clinical trials, and mentoring junior staff. Ideal candidates will have significant experience in the industry, strong leadership capabilities, and familiarity with regulatory standards.

Qualifications

• 4 years total experience in Clinical Data Management, with at least 2 years in a lead capacity.
• Familiarity with clinical trial regulations and data management processes is essential.

Responsibilities

• Manage data processing tasks and timelines for clinical trials.
• Oversee data quality control and compliance with SOPs.
• Train and guide junior staff and data entry teams.

Skills

Leadership

Interpersonal skills

Data management

Education

Bachelor’s degree in a scientific field

Job description

Senior Clinical Data Manager | Global CRO | Full Time | Remote North America

Our client is a well-established mid-sized CRO based in the Toronto Area and known for providing top-notch clinical solutions to a range of small and mid-sized Biotech companies.

They are currently seeking a Senior Clinical Data Manager to join their team in Bridgewater NJ, or remotely within North America. This is a lead role requiring the candidate to have at least 4 years of experience in Clinical Data Management within a CRO or Pharma setting, as well as 2 years of independent Lead experience.

Key Responsibilities :

• Manage data processing tasks and timelines for clinical trials
• Oversee data quality control, ensuring compliance with SOPs and sponsor guidelines
• Lead data management projects, coordinate activities, and develop database validation checks
• Design case report forms (CRFs) and handle quality control
• Train and guide junior staff and data entry teams

Requirements :

• Bachelor’s degree in a scientific field and 2+ years of independent lead experience, 4 years total in DM.
• Familiarity with clinical trial regulations and data management processes
• Strong leadership and interpersonal skills

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