Clinical Research Coordinator I

Centricity Research; Oshawa; On-site; CAD 55,000 - 63,000; Full time

Benefits offered by this job

Health, dental, and vision insurance

Enhanced EAP – mental health support

Flexible PTO + paid holidays

Continuing education reimbursement

401(k)/RRSP with company match

Job summary

Centricity Research in Oshawa is seeking an experienced Clinical Research Coordinator I (CRC I) to join our team at the Oshawa site, with travel to the TOLMC site as needed. You will support clinical research operations by performing administrative and clinical duties, including phlebotomy, under protocol and regulatory requirements.

The role requires a bachelor’s degree in health or science, prior CRC experience, phlebotomy skills, and a willingness to travel to support study activities.

Qualifications

• Bachelor’s degree in health, science, or a related field.
• Prior CRC experience and proficiency with clinical tools.
• Phlebotomy experience and ability to perform blood draws.
• Willingness to travel between Oshawa and TOLMC as needed.

Responsibilities

• Coordinate study visits in compliance with protocol, GCP, and SOPs.
• Document regulatory records and support audits and inspections.
• Perform clinical procedures such as vitals, ECGs, and blood draws.
• Assist with site start-up activities and recruitment efforts.

Skills

Phlebotomy

Clinical coordination

Attention to detail

Education

Bachelor's degree in health/science or related field

Tools

Blood pressure monitors

ECG machines

Weight scales

Job description

Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.

About the Role

We are seeking an experienced full-time Clinical Research Coordinator I (CRC I) to join our research team, primarily based at our Oshawa site, with travel to and support for our TOLMC site as needed. In this role, you will provide additional CRC coverage and support continuity of clinical research operations while performing a mix of administrative and clinical responsibilities. You will work closely with Investigators and the broader research team to ensure study activities are organized, compliant, and aligned with protocol requirements. Prior clinical research coordination experience and phlebotomy skills are required.

What You’ll Do

Study Coordination & Participant Safety

• Conduct study visits in accordance with protocol, GCP, SOPs, and regulatory requirements
• Ensure participant safety and well-being, reporting and documenting adverse events per protocol and regulations
• Perform clinical procedures such as vitals, ECGs, sample collection/processing, and investigational product handling

Recruitment, Screening & Enrollment

• Support recruitment strategies to identify and enroll eligible participants
• Conduct participant screening according to protocol inclusion/exclusion criteria
• Guide participants through the informed consent process and ensure proper documentation
• Schedule and coordinate study visits throughout the participant lifecycle

Study Execution & Data Integrity

• Accurately complete study documentation, regulatory records, and periodic reports
• Prepare for and support monitoring visits, audits, and inspections
• Perform regular quality control (QC) checks on study data and source documents
• Collaborate with investigators, management, and sponsors to ensure study compliance and accuracy
• Contribute to site start‑up activities, including feasibility questionnaires (FQs) and pre-study visits (PSVs)

Quality, Compliance & Site Support

• Prepare for monitoring visits, audits, and maintain regulatory files
• Perform regular quality control checks on source data and documents
• Support lab supply inventory, equipment maintenance, and administrative needs
• Assist with community engagement and outreach events as needed

You Might Be a Great Fit If You:

• Have a bachelor’s degree in a health, science, or research-related field (or equivalent combination of education and experience)
• Have prior experience as a Clinical Research Coordinator and are comfortable with clinical tools like blood pressure monitors, ECG machines, and weight scales
• Have phlebotomy experience and are comfortable performing blood draws
• Understand basic medical terminology, or are eager to learn it quickly
• Are passionate about contributing to clinical trials that impact global health
• Are organized, detail-oriented, and skilled at multitasking in a fast-paced environment
• Are proactive, collaborative, and take ownership of your work
• Value open communication and thrive in a team-driven environment
• Are able to work primarily at our Oshawa site and travel to support our TOLMC site as needed

Why Centricity Research?

Our Mission

We connect people to scientific advancements through groundbreaking research within a deeply human experience.

Our Core Values

• Quality : We aim for excellence and integrity in everything we do - because lives depend on it.
• Care : We show up for each other, our customers, and our mission - always going the extra mile.
• Be the Change You Seek : We're adaptable, forward-thinking, and constantly improving - for the betterment of all.
• One Team : We collaborate, support one another, and succeed together.
• Grow for Good : We grow with purpose - to expand access to research and improve global health.
• Own It : We take initiative, deliver results, and follow through - with passion and accountability.
• Comprehensive health, dental, and vision insurance
• Enhanced EAP – mental health support
• Flexible PTO + paid holidays
• Continuing education reimbursement
• 401(k) / RRSP with company match and immediate vesting

We’re an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provide accommodations during the hiring process upon request.

The pay range for this role is:

55,000 - 62,500 CAD per year (Centricity Research Oshawa Multispecialty)