Senior Clinical Data Manager - HYBRID - Mississauga, Canada

ClinChoice; Mississauga; Hybrid; CAD 80,000 - 110,000; Full time

Job summary

An established industry player is seeking a Senior Clinical Data Manager to join their innovative team in Mississauga, Canada. This hybrid role offers the opportunity to lead multiple data management projects, ensuring high-quality clinical data delivery and client satisfaction. With over 28 years of experience, the company values diversity and promotes a collaborative culture, making it an ideal environment for professional growth. If you're passionate about contributing to a healthier, safer world through innovative drug and device development, this is the perfect opportunity for you.

Qualifications

• 5+ years of data management experience in the pharmaceutical or medical device industry.
• Knowledge of clinical trial processes and regulatory requirements.

Responsibilities

• Lead multiple Data Management projects ensuring timely and quality deliverables.
• Develop and maintain Data Management Plans and electronic Case Report Forms.
• Coordinate data transfer, validation, and database lock procedures.

Skills

Data Management

Clinical Research

Good Clinical Practices

Database Design

User Acceptance Testing

Education

Bachelor’s degree in a science-related field

Tools

EDC (Electronic Data Capture)

Job description

Senior Clinical Data Manager - HYBRID - Mississauga, Canada

Join ClinChoice as a Senior Clinical Data Manager - HYBRID - Mississauga, Canada.

ClinChoice is a global full-service CRO dedicated to professional development and work-life balance, fostering a collaborative “one-team” culture. We are seeking a Senior Data Manager for a permanent role in Mississauga, Canada, on a HYBRID model.

Responsibilities

• Lead multiple Data Management projects, ensuring timely and quality deliverables.
• Review clinical research documents such as protocols, CRFs, reports, and statistical analysis plans.
• Develop and maintain Data Management Plans (DMPs) and electronic Case Report Forms (eCRFs).
• Design database specifications, including eCRF design, user requirements, edit checks, and validation rules.
• Lead EDC database specification processes and develop Data Transfer Agreements with external vendors.
• Perform User Acceptance Testing (UAT), data reviews, and mentor junior Data Managers.
• Coordinate data transfer, validation, and database lock procedures.
• Ensure high-quality clinical data delivery and maintain client satisfaction.
• Assist in study close-out activities and database archiving.

Qualifications

• Bachelor’s degree in a science-related field.
• Minimum 5 years of data management experience in the pharmaceutical or medical device industry preferred.
• Knowledge of Good Clinical Practices, clinical trial processes, and regulatory requirements.
• Experience with clinical database applications such as EDC.

Application Process

Submit your CV to receive acknowledgment. Qualified candidates will be invited for a phone interview. Due to high application volume, only selected candidates will be contacted.

About ClinChoice

ClinChoice is a global CRO with over 28 years of experience, over 4,000 professionals worldwide, and a mission to contribute to a healthier, safer world through innovative drug and device development. We value diversity and are committed to inclusive hiring practices.