Senior Clinical Data Manager

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

Job summary

An established industry player is seeking a Senior Clinical Data Manager to lead data management projects and ensure data quality for clinical trials. This role, which can be performed remotely across North America, requires a strong background in Clinical Data Management and leadership experience. You will be responsible for overseeing data processing tasks, coordinating activities, and training junior staff. Join a dynamic team dedicated to providing top-notch clinical solutions to Biotech companies and make a significant impact in the field. If you are passionate about clinical data and looking for an exciting opportunity, apply now!

Qualifications

• 8+ years of experience in Clinical Data Management within a CRO or Pharma setting.
• 3 years of independent Lead experience required.

Responsibilities

• Manage data processing tasks and timelines for clinical trials.
• Oversee data quality control and ensure compliance with SOPs.

Skills

Clinical Data Management

Leadership Skills

Interpersonal Skills

Data Quality Control

Regulatory Knowledge

Education

Bachelor’s degree in a scientific field

Job description

Direct message the job poster from Warman O'Brien

Recruitment Team Lead | Biometrics at Warman O'Brien

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 8 years of experience in Clinical Data Management within a CRO or Pharma setting, as well as 3 years of independent Lead experience.

Key Responsibilities:

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

Requirements:

1. Bachelor’s degree in a scientific field and 3+ years of independent experience, 6 years total in DM.
2. Familiarity with clinical trial regulations and data management processes
3. Strong leadership and interpersonal skills

Apply now to avoid missing out on this opportunity!

Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Analyst, Other, and Science

Industries

Pharmaceutical Manufacturing and Biotechnology Research