Selected: ๐งช Clinical Research.
Selected: ๐จ๐ฆ Canada โ Remote.
Selected: ๐ Date Added.
๐ 4 days ago
Biostatistician II leading statistical analyses and clinical-trial documentation for Altasciencesโ drug-development programs. Using SAS to support sponsors, regulatory submissions, and preclinical projects.
๐ United States, Canada โ Remote
๐ช๏ธ Kansas โ Remote
๐ต $70k - $90k / year
๐ฐ Private Equity Round on 2017-06
โฐ Full Time
๐ข Junior
๐ก Mid-level
๐งช Clinical Research
๐ฆ H1B Visa Sponsor
๐ป Ghost score 0%
๐ 4 days ago
Clinical Research Associate monitoring sponsor-dedicated clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Ensuring site compliance, patient safety, data quality, and study delivery.
๐ United States, Canada โ Remote
โฐ Full Time
๐ Senior
๐งช Clinical Research
๐ป Ghost score 10%
๐ 5 days ago
Senior Clinical Research Associate monitoring Parexel clinical trials across remote Canadian sites. Managing investigator relationships, patient safety, compliance, recruitment, and study close-out.
๐จ๐ฆ Canada โ Remote
๐ฐ Venture Round on 1990-01
โฐ Full Time
๐ Senior
๐งช Clinical Research
๐ป Ghost score 10%
๐ 6 days ago
Clinical Research Associate II monitoring oncology clinical trials for IQVIA Biotech, a global clinical research services CRO. Managing sites from start-up through close-out.
๐จ๐ฆ Canada โ Remote
๐ต $74.7k - $124.5k / year
๐ฐ $1G Post-IPO Debt on 2023-05
โฐ Full Time
๐ข Junior
๐ก Mid-level
๐งช Clinical Research
๐ป Ghost score 0%
๐ฃ๏ธ๐ซ๐ท French Required
๐ 6 days ago
Clinical Data Manager leading clinical data operations for Indero, a dermatology and rheumatology CRO. Managing EDC databases, data quality, vendors, and database lock activities.
๐จ๐ฆ Canada โ Remote
โฐ Full Time
๐ก Mid-level
๐ Senior
๐งช Clinical Research
๐ป Ghost score 12%
๐ August 24
Senior Clinical Research Associate monitoring phase IIโIV clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Managing investigational sites, regulatory submissions, documentation, and ICH-GCP compliance.
๐ฃ๏ธ๐ฉ๐ช German Required
๐ August 24
Senior Clinical Research Associate monitoring Pfizer clinical trials across remote Canadian investigator sites. Ensuring patient safety, regulatory compliance, recruitment and study closeout.
๐จ๐ฆ Canada โ Remote
๐ต $92.1k - $153.5k / year
๐ฐ Post-IPO Debt on 2023-05
โฐ Full Time
๐ Senior
๐งช Clinical Research
๐ป Ghost score 0%
๐ฃ๏ธ๐ซ๐ท French Required
๐ August 21
Senior Clinical Research Associate monitoring Pfizer clinical trials across Canadian investigator sites. Ensuring patient safety, site quality, GCP compliance and timely study closeout.
๐จ๐ฆ Canada โ Remote
๐ต $73.7k - $122.8k / year
๐ฐ Post-IPO Debt on 2023-05
โฐ Full Time
๐ Senior
๐งช Clinical Research
๐ป Ghost score 0%
๐ฃ๏ธ๐ซ๐ท French Required
๐ August 21
Clinical Trial Manager overseeing monitoring, sites, budgets, and deliverables for early-phase trials at Indero, a Canadian dermatology CRO. Mentoring CRAs and supporting Sponsor operations.
๐จ๐ฆ Canada โ Remote
โฐ Full Time
๐ก Mid-level
๐ Senior
๐งช Clinical Research
๐ป Ghost score 12%
๐ August 21
Clinical Data Manager leading clinical data management for Indero, a dermatology and rheumatology CRO. Managing EDC databases, data quality, vendors, regulatory compliance, and study delivery.
๐ August 21
Clinical Data Manager validating synthetic clinical data rooms, CDISC/SDTM conformance, and cross-file reconciliation. Creating clinical data-management tasks and reference solutions for 24-MAGโs consulting platform.
๐ United States, Canada, +1 more countries โ Remote
๐ฝ New York โ Remote
๐ต $90 - $140 / hour
โฑ Part Time
๐ก Mid-level
๐ Senior
๐งช Clinical Research
๐ป Ghost score 0%
๐ August 21
Clinical biostatistician transforming clinical trial data into SDTM, ADaM, and TLF outputs for 24-MAG. Executing SAP-based analyses and validating traceable Phase IโIII clinical research workflows.
๐ United States, Canada, +1 more countries โ Remote
๐ฝ New York โ Remote
๐ต $110 - $160 / hour
โฑ Part Time
๐ก Mid-level
๐ Senior
๐งช Clinical Research
๐ป Ghost score 0%
๐ August 20
51 - 200
Clinical Data Manager overseeing clinical data rooms for Mercorโs AI-training projects. Ensuring CDISC-compliant datasets, TLFs, narratives, and synthetic data quality.
๐ United States, Canada, +1 more countries โ Remote
๐ต $100 - $150 / hour
๐ฅ Funding within the last year
๐ฐ $350M Series C - Mercor on 2025-10
โณ Contract/Temporary
๐ก Mid-level
๐ Senior
๐งช Clinical Research
๐ป Ghost score 0%
๐ August 17
Senior Clinical Research Associate managing oncology trial sites for Worldwide Clinical Trials, a global contract research organization. Overseeing study start-up, site maintenance, safety reporting, and closeout across Canada.
๐ August 14
Lead Clinical Research Associate coordinating Canadian clinical trials for PSI, a contract research organization. Managing monitors, sites, compliance, training, enrollment, and clinical supplies across Phase IโIII studies.
๐จ๐ฆ Canada โ Remote
๐ต $124k - $153k / year
โฐ Full Time
๐ Senior
๐งช Clinical Research
๐ป Ghost score 0%
๐ August 14
Senior Clinical Research Associate conducting onsite monitoring and regulatory support for a global medical research company in Canada. Managing clinical-trial sites, CRFs, queries, audits, and study submissions.
๐จ๐ฆ Canada โ Remote
๐ต $120k - $150k / year
โฐ Full Time
๐ Senior
๐งช Clinical Research
๐ป Ghost score 0%
๐ฃ๏ธ๐ซ๐ท French Required
๐ August 11
Real-world biostatistician designing safety and observational studies from EMR and claims data for Syneos Health. Supporting drug development, HEOR, regulatory strategy, and market access.
๐ United States, Canada โ Remote
๐ต $80.6k - $145k / year
โฐ Full Time
๐ก Mid-level
๐ Senior
๐งช Clinical Research
๐ฆ H1B Visa Sponsor
๐ป Ghost score 0%
๐ August 10
Senior Clinical Research Associate conducting Phase II/III trial monitoring for a global medical research company. Managing sites, regulatory submissions, audits, and study-team communications in Canada.
๐จ๐ฆ Canada โ Remote
๐ต $120k - $150k / year
โฐ Full Time
๐ Senior
๐งช Clinical Research
๐ป Ghost score 0%
๐ July 28
Lead Clinical Research Associate at PSI coordinating clinical project activities and ensuring compliance. Managing teams and communication across clinical trial phases within the oncology field.
๐จ๐ฆ Canada โ Remote
๐ต $124k - $153k / year
โฐ Full Time
๐ Senior
๐งช Clinical Research
๐ป Ghost score 2%
๐ July 17
Clinical Research Associate managing site qualifications and monitoring for clinical studies at Syneos Health. Utilizing ICH/GCP Guidelines to ensure compliance and support patient recruitment.
๐จ๐ฆ Canada โ Remote
โฐ Full Time
๐ข Junior
๐ก Mid-level
๐งช Clinical Research
๐ป Ghost score 24%
+12 More Clinical Researcher Jobs Available!
The average salary for remote clinical researchers in Canada is CA$140,269 per year. This is based on data from 83 job openings. Our advanced AI searches the internet for remote job openings and posts them on our website. We use the salary data from these job postings to calculate salary expectations.
Below is a breakdown of salary data by years of experience:
| Experience | Number of roles analyzed | Average Salary |
|---|---|---|
๐ข Junior Clinical Researcher (1-2 yrs) | 22 | CA$116,766 |
๐ก Mid-level Clinical Researcher (2-4 yrs) | 16 | CA$93,750 |
๐ Senior Clinical Researcher (5-9 yrs) | 42 | CA$166,437 |
๐ด Lead Clinical Researcher (10+ yrs) | 3 | CA$194,375 |
We analyzed 54 job listings in the last year and found it takes about 42 days for employers to close a job opening.
We reviewed 83 job postings and found the top 10 skills employers are asking for most often are:
You need strong analytical and research skills, proficiency in data management and statistical software, and a solid understanding of clinical trial protocols. Effective communication, attention to detail, and problem-solving skills are also essential.
Typically, you need a degree in a related field such as life sciences, nursing, or public health. A master's degree or PhD may be preferred. Certification in clinical research, such as from ACRP or SOCRA, can also be advantageous.
Responsibilities include designing and managing clinical trials, monitoring trial progress, ensuring compliance with regulations, collecting and analyzing data, and reporting findings. You may also work closely with investigators and regulatory bodies.
Benefits include the flexibility to work from anywhere, reduced commuting time, a better work-life balance, and opportunities to contribute to significant healthcare advancements. Remote positions may also offer access to a wider range of job opportunities.
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