Clinical Data Manager / / (full-time, remote)

Everest Clinical Research.; Regina; Remote; CAD 70,000 - 90,000; Full time

Job summary

Everest Clinical Research is hiring Clinical Data Managers who will plan and execute data management activities for clinical trials. Candidates should have a background in health or pharmaceutical sciences and a strong understanding of clinical trial data management. This remote role offers flexibility within Canada and seeks individuals skilled in leadership and data processes.

Qualifications

• At least 2 years of experience in clinical data management for Bachelor's degree holders.
• Deep understanding of clinical trial data management concepts.
• Strong leadership skills to manage data projects.

Responsibilities

• Plan and manage data processing and management activities.
• Lead data management projects and define quality control processes.
• Validate electronically captured data and prepare progress reports.

Skills

Leadership

Data Management

Quality Control

Education

Bachelor’s degree in health or pharmaceutical sciences

Master’s/Ph.D. in related fields

Job description

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of clinical research services to pharmaceutical, biotechnology, and medical device industries worldwide. We work with leading companies and advanced drugs, biologics, and medical devices in development.

Founded in 2004 and headquartered in Markham, Ontario, Canada, Everest has grown from a statistical and data management center of excellence to a comprehensive CRO with additional sites in the USA, China, and Taiwan.

Known for high-quality deliverables, superior customer service, and flexibility, Everest continues to experience significant growth. Our core values include quality, customer focus, and flexibility.

We are seeking dedicated, skilled, and customer-focused individuals to join our team as Clinical Data Managers at our Toronto/Markham location or remotely anywhere in Canada, following our Work from Home policy.

Key Responsibilities:

1. Plan, manage, and execute data processing and management activities for assigned projects, ensuring timely and accurate completion in line with sponsor requirements.
2. Lead data management projects, applying project management skills to coordinate timelines and activities.
3. Specify and develop database validation checks for studies, including standard and therapy-specific modules.
4. Define and monitor data flow and quality control processes according to SOPs and industry standards, and train site monitors on these processes.
5. Design and review CRFs and database schemas; test data entry screens.
6. Validate electronically captured data, write queries for discrepancies, and build a query library for common modules.
7. Perform QC procedures during and after the trial.
8. Train and supervise data entry and junior data management staff.
9. Prepare and distribute study progress reports.
10. Assist in resolving data coding discrepancies.
11. Maintain documentation for data management and assist in archiving study data.
12. Support QA personnel in quality assurance procedures.

Qualifications and Experience:

1. Bachelor’s degree in health, pharmaceutical sciences, or related fields with at least 2 years of clinical data management experience, or a Master’s/Ph.D. with at least 1 year of relevant experience.
2. Deep understanding of clinical trial data management concepts, processes, and regulations.
3. Strong leadership skills and a desire to excel in managing data projects.