Senior Clinical Data Manager

Warman O'Brien; Lac-Brome; Remote; CAD 85,000 - 120,000; Full time

Job summary

A leading Global CRO is seeking a Senior Clinical Data Manager for a key leadership role. The position focuses on overseeing clinical data quality, managing trials, and mentoring junior staff, requiring strong expertise in data management and clinical regulations. This is a remote opportunity available to candidates across North America.

Qualifications

• At least 4 years experience in Clinical Data Management.
• 2+ years of independent Lead experience.
• Familiarity with clinical trial regulations.

Responsibilities

• Manage data processing tasks and timelines for clinical trials.
• Oversee data quality control, ensuring compliance with SOPs.
• Lead data management projects and train junior staff.

Skills

Leadership

Interpersonal skills

Data quality control

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

Apply now to avoid missing out on this opportunity!