Senior CRA
About the role
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Senior Clinical Research Associate (SCRA)
Location: Montreal Canada
At ICON, it's our people that set us apart.
As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?
You MUST have minimum 1 year of EXPERIENCE as a CLINICAL RESEARCH ASSOCIATE to be considered.
Would you like to work for ICON, the highest ranked Clinical Research Organization in the best large employers listing Forbes for the third year in 2019?
As a top five Clinical Research Organization in the world, we are looking to strengthen our Clinical Operations team in the US. As a CRA you will work independently and actively handle all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.
You will be supported with manageable sites & protocols, a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and eligible for the annual performance bonus? Additionally, we have innovative technology and provide excellent training to ensure better outcomes.
You will possess:
- Minimum of 3 years of active independent field monitoring experience- all types of visits.
- Minimum 2 years of Oncology experience as a CRA
- Deep understanding of ICH GCP Compliance.
- Excellent time management and social skills
- Highly motivated with a phenomenal eye for detail.
- Ability to travel 65-75% of the month.
- Bachelor's degree in a life science or related discipline OR RN/LPN with 4 years related experience.
- Bi-lingual - English and French fluency required.
Benefits of working with ICON:
- Comprehensive benefits package including premium salary
- Bonus
- Paid holidays
- Company cell phone and equipment
- Market leading PTO
- Culture of teamwork and collaboration
- People who motivate and face challenges together.
- Innovative technology
We care about our people and your passion, as they are the key to our success and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term career. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of ICON.
Apply today for an immediate telephone interview.
ICON Plc is an equal opportunity employer. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
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IndustryContent type
BlogsPublish date
12/01/2025
Summary
How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
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BlogsPublish date
11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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