Associate in quality control of participant selection tests for clinical trials

Altasciences; Montreal; On-site; CAD 40,000 - 70,000; Full time

Job summary

An established industry player is seeking an Associate in quality control for participant selection tests in clinical trials. This role is crucial in ensuring that collected data meets all study protocols and complies with Good Clinical Practices. You will be responsible for performing quality control checks, correcting data, and preparing study binders. The position offers a collaborative environment where your contributions will directly impact healthcare outcomes. If you have a keen eye for detail and a passion for clinical research, this opportunity is perfect for you.

Benefits

Health/dental/vision insurance

RRSP with employer match

Paid leave

Employee assistance programs

Training

Referral bonuses

Performance reviews

Free parking

Qualifications

• 1+ year of experience in a clinical research environment is an asset.
• Knowledge of clinical trials is a plus.

Responsibilities

• Perform live quality control of screening data to ensure compliance.
• Identify error trends and report them to management.
• Schedule participant appointments and verify blood samples.

Skills

Knowledge of Good Clinical Practices

Bilingual in French and English

Excellent organizational skills

Good communication skills

Education

DEC or relevant experience

Job description

Associate in quality control of participant selection tests for clinical trials

Join to apply for the Associate in quality control of participant selection tests for clinical trials role at Altasciences

About The Role

The Associate in quality control of participant selection tests for clinical trials will perform quality control of data collected during the screening phase of a clinical trial. The role involves ensuring all data complies with study protocols, Good Clinical Practices (GCP), and Standard Operating Procedures (SOPs).

What You’ll Do Here

• Perform live quality control (QC) of all screening data to ensure compliance with study protocols and SOPs.
• Ensure all corrections to raw and derived data are completed.
• Identify error trends and report them to management.
• Print laboratory results and update participant files.
• Schedule participant appointments via phone.
• Verify blood samples between Clinical Research Organizations.
• Respond to QA reports and data management queries, generate report deviations as needed.
• Prepare study binders.

What You’ll Need To Succeed

• DEC or relevant experience and education.
• At least 1 year of experience is an asset.
• Knowledge of Good Clinical Practices.
• Bilingual in French and English.
• Experience in a clinical research environment or knowledge of clinical trials is a plus.
• Excellent organizational and prioritization skills.
• Good communication skills.

What We Offer

• On-site position at Montreal office (1100 Beaumont), accessible by public transit and with free parking.
• Availability between 9 am and 7 pm, with flexibility for overtime and occasional weekends.

Benefits include health/dental/vision insurance, RRSP with employer match, paid leave, employee assistance programs, training, referral bonuses, and performance reviews.

Altasciences is committed to diversity and inclusion, offering accommodations for persons with disabilities during recruitment. Join us to make a meaningful impact in healthcare.