Senior Clinical Data Specialist (FSP) – Canada Remote

Join Fortrea as a Senior Clinical Data Specialist within our Functional Service Provider (FSP) model where you will play a critical role in ensuring highquality clinical data that supports global drug development. This fully remote position offers the opportunity to contribute meaningfully across clinical programs while collaborating with global teams.

This is a full-time home-based position in Canada that will require willingness to work flexible hours as needed to meet business needs.

Key Responsibilities

• You will review clinical trial data in accordance with Global Data Management Plans and standardized data management processes to identify missing incomplete erroneous or implausible data.
• You will run diagnostics special listings reconciliation discrepancy outputs and other ancillary programs supporting clinical data review.
• You will generate track and resolve data queries to ensure highquality complete and accurate clinical data.
• You will conduct aggregate data reviews by patient site and study level to identify patterns inconsistencies compliance issues or potential safety concerns.
• You will apply quality control procedures ensuring all deliverables meet Fortrea and client data quality standards.
• You may review project documentation such as protocols CRFs/eCRFs Data Management Plans and data review guidelines.
• You will assist in developing Data Management Plans Quality Management Plans and data review guidance documents.
• You will support review of database design eCRF annotation and development/testing of data validation checks and special listings.
• You may support the Lead Data Manager or Lead Data Reviewer in timeline planning milestone tracking and crossfunctional coordination.
• You will support internal and client audits address findings and ensure documentation is compliant and inspectionready.
• You may mentor or coach junior staff on project-specific and global processes.
• And all other duties as needed or assigned.

Required Qualifications

• Bachelors degree in life sciences health sciences information technology or a related field; equivalent experience will be considered.
• 46 years of Clinical Data Management experience.
• Working knowledge of clinical trial processes data management workflows clinical operations and biometrics.
• Strong timemanagement skills with the ability to meet productivity metrics and timelines.
• Ability to work effectively both independently and collaboratively.
• Strong organizational interpersonal and written communication skills.
• Knowledge of medical terminology or scientific background preferred.

Preferred Qualifications

• Strong understanding of Fortrea systems SOPs and organizational structure.
• Two or more years of Electronic Data Capture (EDC) experience.
• Prior experience in global studies or FSP-based delivery models.

Work Environment

• Work is performed in an office environment with exposure to electrical office equipment.
• Occasional drives to site locations with some domestic and international travel.

Physical Requirements

• Frequently stationary for 68 hours per day.
• Repetitive hand movements with the ability to make fast simple repeated motions using fingers hands and wrists.
• Occasional crouching and stooping; frequent bending and twisting of the upper body and neck.
• Ability to access and use various computer software applications developed inhouse or offtheshelf.
• Light to moderate lifting and carrying (e.g. luggage and laptop) up to 1520 lbs.
• Regular and consistent attendance required.
• Varied hours may be required depending on project needs.

Pay Range CAD annually

Benefits: All job offers will bebased on a candidates skills and prior relevant experience applicabledegrees/certificationsas well as internal equity and market data.

Application Deadline: 02/23/26

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