Clinical Research Associate with Visa Sponsorship

About the Company

Join IQVIA, a global leader in human data science. We are dedicated to using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. We are committed to improving patient outcomes and accelerating clinical development worldwide.

Job Description

We are seeking a highly motivated and detail-oriented Clinical Research Associate (CRA) to join our dynamic team in Edmonton, Alberta. This is a full-time, hybrid position, offering the flexibility of both remote work and essential on-site presence at clinical sites and potentially our local office. This unique opportunity includes visa sponsorship for qualified international candidates, demonstrating our commitment to attracting top global talent. As a CRA, you will play a crucial role in managing and monitoring clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements. Your expertise will directly contribute to the successful execution of studies that bring life-changing treatments to patients.

Key Responsibilities

• Conducting pre-study, initiation, routine monitoring, and close-out visits for clinical trial sites.
• Ensuring compliance with study protocols, regulatory guidelines, and Good Clinical Practice (GCP) standards.
• Verifying the accuracy and completeness of case report forms (CRFs) and source documents.
• Reviewing investigator site files (ISF) for accuracy, completeness, and regulatory compliance.
• Managing study-related supplies, drug accountability, and equipment at assigned sites.
• Building and maintaining strong professional relationships with investigators and site staff.
• Identifying and resolving site-related issues, escalating complex problems to the project team.
• Preparing monitoring reports and follow-up letters in a timely and accurate manner.
• Participating in investigator meetings and other project-related discussions as required.
• Providing ongoing support and training to site personnel to ensure successful trial conduct.

Required Skills

• Bachelor's degree in a life science, nursing, pharmacy, or related field.
• Minimum of 24 months (2 years) of experience as a Clinical Research Associate or equivalent in a CRO or pharmaceutical company setting.
• Demonstrated knowledge of Good Clinical Practice (GCP) and applicable regulatory guidelines.
• Excellent communication, interpersonal, and organizational skills.
• Ability to travel frequently within the region and occasionally internationally, as required for site monitoring.
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Strong problem-solving abilities and attention to detail.
• Eligibility for visa sponsorship in Canada.

Preferred Qualifications

• Master's degree or higher in a relevant scientific or medical field.
• Experience across multiple therapeutic areas, such as Oncology, Cardiology, or Neuroscience.
• Certification as a Clinical Research Associate (e.g., ACRP or SOCRA).
• Familiarity with the Canadian regulatory landscape for clinical trials.
• Ability to speak French is an asset for supporting bilingual sites, though not mandatory.

Perks & Benefits

• Comprehensive health, dental, and vision insurance plans.
• Generous paid time off and holiday schedule.
• Retirement savings plan with company match.
• Opportunities for professional development and continuous learning.
• Access to a global network of scientific and clinical experts.
• Employee assistance program and wellness initiatives.
• Relocation assistance and visa sponsorship support for eligible candidates.
• A collaborative and supportive work environment committed to innovation.

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