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- ICON PlcMontréal, QC
- Full-time
- You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
- Life assurance and disability coverage.
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- ICON PlcMontréal, QC
- Full-time
- You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
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- ICON PlcMontréal, QC
- Full-time
- Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research…
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- Salary Search: Senior CRA salaries
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- ICON PlcBurlington, ON
- Full-time
- You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
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- ICON PlcBurlington, ON
- Full-time
- Performing data review and resolution of queries to maintain high-quality clinical data.
- You will bring relevant clinical trial monitoring experience, along…
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- ICON PlcBurlington, ON
- Full-time
- Performing data review and resolution of queries to maintain high-quality clinical data.
- You will bring relevant clinical trial monitoring experience, along…
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- ICON PlcBurlington, ON
- Full-time
- Minimum 2–3 years of relevant experience working in clinical trials.
- Develop and implement site-specific action plans to accelerate patient recruitment and…
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- ICON PlcMontréal, QC
- Full-time
- Oversees and tracks clinical research-related payments.
- 5 years of experience in clinical research or combined experience in Clinical Research and Finance/…
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- ICON PlcMontréal, QC
- Full-time
- Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
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- ICON PlcMontréal, QC
- Full-time
- Document proper destruction of clinical supplies.
- Update clinical trial databases (CTMS) and trackers.
- Collate, distribute/ship, and archive clinical documents.
- ICON PlcBurlington, ON
- Full-time
- You will bring relevant clinical research experience, along with the following qualifications and skills.
- You will contribute to clinical research activities,…
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- ICON PlcBurlington, ON
- Full-time
- ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
View similar jobs with this employerICON PlcBurlington, ON- $108,576–$135,720 a year
- Full-time
- Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research…
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Study Start Up CRA
Job details
Full job description
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.
What You Will Do:
Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
- Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
- Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
- Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
- Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.
Your Profile:
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
- Excellent written and verbal communication in English
- Good social skills enabling you to deal with queries in a timely manner
- Willingness to travel as required (approximately 60%)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request .
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