About the Company
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and contract research services to the life sciences industry. Formed through the merger of IMS Health and Quintiles, IQVIA applies human data science—leveraging the breadth of human science and data science—to help customers find smarter solutions and redefine medical innovation. We enable healthcare companies to accelerate the clinical development and commercialization of innovative medicines that improve patient lives. Join our dedicated team in London, Ontario, and contribute to cutting-edge clinical research.
Job Description
We are seeking a highly motivated and detail-oriented Clinical Research Associate to join our dynamic team in London, Ontario. This role offers an exceptional opportunity for individuals looking to advance their career in clinical research with the support of a global relocation package. As a Clinical Research Associate, you will play a critical role in the oversight of clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements. You will be responsible for monitoring study sites, verifying data accuracy, and providing comprehensive support to investigators. This position is ideal for someone with foundational experience in clinical research or a related scientific field, eager to grow within a leading global Contract Research Organization (CRO). Full training and ongoing development will be provided to ensure your success.
Key Responsibilities
- Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols, SOPs, GCP, and regulatory requirements.
- Verify the rights and well-being of human subjects are protected, and that informed consent is obtained and documented.
- Ensure the integrity of clinical data through source document verification, query resolution, and adherence to data management plans.
- Provide guidance and support to clinical trial sites on protocol compliance, subject recruitment, and regulatory documentation.
- Review and approve investigator site files and essential documents.
- Communicate effectively with investigators, study coordinators, and internal project teams regarding study progress and issues.
- Identify and resolve site-related issues in a timely and efficient manner.
- Assist in the preparation and review of study-related reports and documentation.
- Participate in investigator meetings and internal project team meetings.
Required Skills
- Bachelor's degree in a life science, nursing, pharmacy, or related field.
- Minimum of 12 months of experience in clinical research, healthcare, or a related scientific role.
- Understanding of medical terminology and clinical research processes.
- Excellent written and verbal communication skills in English.
- Strong organizational skills and attention to detail.
- Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to travel frequently to clinical sites.
- Demonstrated ability to work independently and as part of a team.
- Valid driver's license.
Preferred Qualifications
- Familiarity with Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Previous experience as a Clinical Research Coordinator (CRC) or in a similar site-based clinical role.
- Master's degree or higher in a relevant scientific discipline.
- Experience with Electronic Data Capture (EDC) systems.
- Proficiency in an additional language.
Perks & Benefits
- Competitive salary and performance-based bonuses.
- Comprehensive global relocation package, including visa sponsorship and settling-in support.
- Full health, dental, and vision insurance coverage.
- Generous paid time off and holidays.
- Retirement savings plan with company match.
- Opportunities for continuous learning and professional development.
- Mentorship programs and career advancement pathways.
- Access to cutting-edge technologies and diverse therapeutic areas.
- Dynamic and inclusive work environment.
- Employee assistance program.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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