Senior Clinical Data Manager

Warman O'Brien; Banff; Remote; CAD 80,000 - 120,000; Full time

Job summary

A well-established mid-sized CRO is seeking a Senior Clinical Data Manager, offering remote opportunities across North America. This lead role demands significant Clinical Data Management experience to manage project timelines, oversee data quality, and train junior staff. Candidates should possess strong leadership skills and familiarity with clinical trial regulations.

Qualifications

• 4+ years of experience in Clinical Data Management, with at least 2 years in a lead role.
• Familiarity with clinical trial regulations and data management processes.
• Strong leadership and interpersonal skills.

Responsibilities

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

Skills

Leadership

Interpersonal Skills

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!