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Clinical Quality Control Associate II
Altasciences. Conduct quality control review of clinical trial data.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in conducting quality control reviews of clinical trial data while ensuring compliance with Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). Strong communication skills in both French and English, along with a detail-oriented approach to managing data queries and maintaining confidentiality.
Highest-signal resume keywords
Quality Control ReviewGood Clinical Practices (GCP)Data Query ManagementBilingual Communication (French and English)Detail Oriented
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Quality ControlData CompilationDeviation TrackingClinical Trial DocumentationProtocol Compliance
Soft Skills
Customer Service FocusedDetail OrientedOrganizational SkillsProblem ResolutionRelationship Building
Tools & Technologies
Microsoft Office
Industry Keywords
Clinical TrialsStandard Operating Procedures (SOPs)ConfidentialityQuality SystemsStudy Protocol
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Conduct quality control review of clinical trial data.
- Work with the Quality Systems team to complete QC-related tasks.
- Perform tasks in compliance with study protocol, Good Clinical Practices (GCP), and Standard Operating Procedures (SOPs).
- Report, track, and escalate errors and/or trends that may require re-training.
- Compile data, maintain computerized files, and update deviation tracking systems.
- Record, track, and ensure resolution of data queries.
- Communicate issues and problem resolutions to departmental supervisors and managers.
- Maintain confidentiality of clinical trial participants and sponsors.
- Maintain and advocate a high level of quality and customer service.
- Document and/or report clinical trial-related deviations.
- Mentor and coach Quality Systems team members.
- Understand protocol-driven timed study events and acceptable collection windows.
- Perform other tasks as assigned by management.
Requirements
What you’ll need- High School Diploma completed.
- Related work experience an asset.
- Good Communication in French and English.
- Detail oriented, well organized, customer service focused, able to work in fast-paced environment.
- Software: Microsoft Office.
- Strong attention to details.
- Personal/professional integrity and proven discretion in handling confidential information.
- Ability to develop strong trusting relationships in order to gain support and achieve results.
- Capable of managing multiple conflicting priorities.
- Must be self-directed, motivated and have a willingness to take initiative.
- The candidate must be able to lift up to 25 pounds.
- Fluency in English is an essential requirement for the position.
- Candidate needs to be available between 7am and 7pm and 1 every 3 week-ends.
Benefits
Comp & perks- Regular full-time position; 37.5 hours a week
- Accessible by metro (L'Acadie)
- Free parking for employees
- Health/dental/vision insurance plans
- RRSP with employer match
- Paid vacation and statutory vacations
- Paid sick leave and bereavement leave
- Employee assistance and telehealth programs
- Training and development programs
- Employee orientation bonus program
- Annual performance reviews