Clinical Quality Control Associate II

Altasciences; Montreal; On-site; CAD 52,000 - 68,000; Full time

Benefits offered by this job

On-site location in Montreal (1200)

Free parking for employees

Metro access (L'Acadie)

Health/dental/vision insurance

RRSP with employer match

Job summary

Altasciences is seeking a Clinical Quality Control Associate in Montreal to support QC review of clinical trial data in alignment with GCP and SOPs. You will work with the Quality Systems team to complete QC tasks, ensuring data integrity and regulatory compliance.

The role requires strong attention to detail, fluency in French and English, and the ability to manage multiple priorities in a fast-paced environment. On-site position with benefits included.

Qualifications

• High school diploma required; related work experience an asset.
• Detail-oriented with strong organizational and communication skills.
• Ability to maintain confidentiality and handle data with discretion.

Responsibilities

• QC review of clinical trial data and support to Quality Systems.
• Record, track and resolve data queries and deviations.
• Communicate issues to supervisors and managers promptly.
• Maintain confidentiality of trial participants and sponsors.
• Mentor and coach team members on quality processes.

Skills

Bilingual FR/EN

Detail oriented

Time management

Communication skills

Self-motivated

Education

High School Diploma

Tools

Microsoft Office

Job description

About The Role

The Clinical Quality Control Associate is responsible for the quality control (QC) review of clinical trial data and working with the Quality Systems team to complete QC related tasks. The Clinical Quality Control Associate will conduct tasks performed within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).

About The Role

The Clinical Quality Control Associate is responsible for the quality control (QC) review of clinical trial data and working with the Quality Systems team to complete QC related tasks. The Clinical Quality Control Associate will conduct tasks performed within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).

What You’ll Do Here

• Report, track and elevate (if necessary) errors and/or trends that may require re-training, as required by location.
• Compile data and maintain computerized files and/or update deviation tracking systems.
• Record, track and ensure the resolution of data queries.
• Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
• Ensure the confidentiality of clinical trial participants and sponsors is respected.
• Maintain and advocate a high level of quality and customer service within the department.
• May document and/or report clinical trial related deviations (i.e. SOP, protocol).
• Act as a mentor and coach the Quality Systems team members.
• Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events.
• Other tasks as assigned by management

What You’ll Need To Succeed

• 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.

Altasciences Strives To Provide a French Working Environment For Its Employees In Quebec. Although As Part Of Its Francization Program Has Taken All Reasonable Steps To Avoid Imposing The Above‑mentioned Requirement. Fluency In English Is An Essential Requirement For The Position Of Clinical Quality Control Associate Including, But Not Limited To, For The Following Reasons

• The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.

What We Offer

• Regular full-time position; 37.5 hours a week.
• Candidate needs to be available between 7am and 7pm and 1 every 3 week-ends.
• On site, Montreal site (1200 Beaumont).
• Accessible by metro (L'Acadie); Free parking for employees.

Altasciences offers a wide range of benefits to help employees live healthy and satisfying lives, both on and off the job.

Altasciences Benefits Include

• 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

Altasciences' incentive programs include

• Training and development programs
• Employee orientation bonus program
• Annual performance reviews