Posted 21 days ago
Clinical Research Coordinator I
@ Centricity Research
Oshawa, Ontario
Overview
Centricity Research is hiring a full-time Clinical Research Coordinator I, based primarily at its Oshawa site with travel to its TOLMC site as needed. The role covers study visits, participant screening and enrollment, clinical procedures such as blood draws, and regulatory documentation. Prior clinical research coordination experience and phlebotomy skills are required.
Pay:
$55,000–$62,500 a year
Responsibilities:
- Conduct study visits per protocol and GCP
- Recruit, screen, and enroll eligible participants
- Complete study documentation and regulatory records
- Prepare for monitoring visits, audits, and inspections
- Perform quality control checks on source data
Requirements summary:
- Prior Clinical Research Coordinator experience
- Phlebotomy experience and comfort with blood draws
- Bachelor's degree in health, science, or research, or equivalent
- Familiarity with clinical tools such as ECG machines and BP monitors
- Organized and detail-oriented in a fast-paced environment
Tools & skills
Benefits mentioned
Source and dates
Employer career site / ATS feed · rippling
- Employer posting date
- 2026-10-16
- First seen by our source
- 2026-10-16
- Source record updated
- 2026-10-16
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Mid level |
| Department | Allied health |
| Hours per week | 40 (estimated) |
| Travel | air: none · ground: minimal |
| Work setting | Office |
| Position | Sitting and standing |
| Physical demands | physical low · computer moderate |
| Languages | English |
| Education | Bachelor’s degree (required) |
| Fields of study | health, science, research |
| Perks mentioned | Generous paid time off, Flexible hours, Retirement plan, Tuition support, Wellness |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Centricity Research
Saved company profile
Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.
Revolutionizing Research and Changing Lives!
Full company description
Centricity Research is an integrated research organization (IRO) with more than 40 wholly owned and integrated clinical research offices across North America. The company conducts Phase I-IV clinical research in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials. For more than 25 years, the organization’s founders have worked to revolutionize research by investing in the people and technology needed to deliver outstanding clinical trial experiences, earning numerous awards including “Best Places to Work” and recognition for “Outstanding Diversity in Clinical Research.” Jobseekers: Apply here >> https://centricityresearch.applytojob.com/apply
- LinkedIn followers
- 22,878
- People associated on LinkedIn
- 250
- Reported office locations
- 910 Talbotton Rd, Columbus, Georgia 31904, US
- 1929 Bayview Ave, 106, Toronto, Ontario M4G 3E8, CA
- Business categories
- Service Industry
- Consulting
- Biotechnology
- Life Science
- Other recorded names
- Centricity Research
- Specialties
- Clinical Research
- Primary Care
- Phase I to IV
- Drug Development
- Clinical Trials
- Clinical Studies
- and Biotechnology
- Profile identifies a recruitment agency
- No
- Reported total investment
- 0
Currency and observation date were not supplied; this is not a current valuation or a funding round.
Centricity Research is an integrated research organization (IRO) with more than 40 wholly owned and integrated clinical research offices across North America. The company conducts Phase I-IV clinical research in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials. For more than 25 years, the organization’s founders have worked to revolutionize research by…
| Field | Value |
|---|---|
| Industry | Biotechnology Research |
| Company size | 201-500 employees |
| Headquarters | Columbus, Georgia |
| Organization type | Privately Held |
| Specialties | Clinical ResearchPrimary CarePhase I to IVDrug DevelopmentClinical TrialsClinical Studiesand Biotechnology |
| Open jobs on Jobsy | 5 |
| View page |
Join the Centricity Research Team!
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.
Benefits
- 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
Ready to Apply?
We’d love to hear from you – apply now!
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.
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