AI Biotech Job Matching

Clinical Research Coordinator Jobs — Ranked by Your Qualification

Clinical research coordinator roles are accessible to life sciences graduates and experienced healthcare professionals alike. These roles are ranked by qualification match for candidates transitioning from academic lab work, nursing, or direct CRC experience.

5 matched roles shown

$68k average salary

AI-scored by qualification match

Ranked Roles — Best Match First

Each role is scored based on how well a typical clinical research coordinator jobs candidate qualifies. Upload your resume to get scores based on your specific background.

Clinical Research Coordinator I

University Health Network · Toronto, ON

88 match

💼 Full-time 💰 $54k–$68k ⏱️ 0–2 years

✓ Academic medical centre CRC I roles accept new graduates with GCP certification and strong organizational skills; clinical or lab background is sufficient.

GCPSource DocumentationIRB / REBPatient SchedulingSafety Reporting

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Clinical Research Associate — Oncology

ICON plc · Remote / Canada

80 match

💼 Full-time 💰 $65k–$85k ⏱️ 2–4 years

✓ CRO CRA roles require site monitoring experience and GCP certification; oncology background is preferred but any therapeutic area experience qualifies.

⚠ Missing: Oncology trial experience (helpful)

Site MonitoringGCPProtocol ReviewSDV / SDRSponsor Reporting

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Clinical Trials Coordinator

Pfizer Global Trials · Hybrid — Multiple US Cities

84 match

💼 Full-time 💰 $58k–$74k ⏱️ 1–2 years

✓ Pfizer trial coordinator roles use in-house EDC and CTMS training; GCP certification plus any healthcare or research coordination experience qualifies.

Medidata Rave / EDCCTMSGCPInformed ConsentAE Reporting

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Study Coordinator — Phase II/III Trials

Parexel International · Various Canada / USA

79 match

💼 Full-time 💰 $60k–$78k ⏱️ 1–3 years

✓ Phase II/III coordinator roles at CROs like Parexel accept health science graduates with GCP and 1 year of research coordination or clinical experience.

⚠ Missing: Phase III monitoring depth

GCPRegulatory SubmissionseSourceCTMSSite Management

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Drug Safety Associate (Pharmacovigilance)

PPD / Thermo Fisher · Remote / USA

82 match

💼 Full-time 💰 $55k–$72k ⏱️ 0–2 years

✓ Pharmacovigilance associate roles are accessible to science graduates with basic clinical knowledge; GCP awareness and detail orientation are the primary qualifiers.

Adverse Event ProcessingMedDRA CodingE2B ReportingICH E6/E2A/E2DSafety Database (Argus)

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See Which of These You Actually Qualify For

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Most In-Demand Skills for These Roles

These are the skills that appear most frequently in job postings and determine your match score.

ICH GCP (E6 R2)

Protocol Adherence

Source Documentation

IRB / REB Submissions

eSource / EDC Systems

Adverse Event Reporting

Informed Consent Process

Regulatory Binder Maintenance

Patient Scheduling & Retention

Safety Reporting (SAE/AE)

Sponsor Audit Preparation

CTMS

Salary Ranges

Typical compensation in Canada and the US. Actual offers vary by location, company size, and experience level.

Entry Level

$52k

0–2 years experience

Mid Level

$68k

2–5 years experience

Senior Level

$90k

5+ years experience

Who Should Apply

Candidates most likely to qualify for these roles.

BSc or BHSc graduates in biology, health sciences, nursing, or life sciences. Registered nurses (RN) and practical nurses (PN) transitioning to clinical research are highly competitive. GCP (ICH E6) certification is a strong qualifier and can be obtained before applying. Experience with patient-facing roles, protocol documentation, or IRB/REB submissions significantly improves match scores.

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