About the Company
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to pushing the boundaries of human science and data science to make the greatest impact possible to patients. With a global presence and diverse team, we offer unparalleled opportunities for growth and innovation.
Job Description
We are seeking a highly motivated and detail-oriented Clinical Research Associate (CRA) to join our dynamic team in Kamloops, BC. This unique opportunity includes a comprehensive global relocation package, designed to support your move and integration into our vibrant community and organization. As a CRA, you will play a crucial role in the execution and monitoring of clinical trials, ensuring compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. You will be responsible for building strong relationships with investigative sites, supporting the collection of high-quality data, and contributing to the successful completion of groundbreaking research that impacts patient lives globally. This role offers excellent professional development and the chance to work on diverse therapeutic areas.
Key Responsibilities
- Conduct on-site and remote monitoring visits to ensure subject safety, data integrity, and protocol compliance.
- Verify that informed consent is properly obtained and documented.
- Review source documents and Case Report Forms (CRFs) against trial protocols and regulatory guidelines.
- Manage study site performance, including patient recruitment and retention strategies.
- Ensure accurate and timely data submission and query resolution.
- Provide training and support to investigational site staff on study protocols and procedures.
- Prepare and submit monitoring reports and follow-up letters.
- Assist with regulatory submissions and essential document collection.
- Maintain effective communication with site staff, project managers, and internal teams.
Required Skills
- Bachelor's degree in a life science or related field.
- Minimum of 2 years of experience as a Clinical Research Associate or equivalent clinical trial experience.
- Thorough understanding of ICH-GCP guidelines and relevant regulatory requirements.
- Excellent communication, organizational, and interpersonal skills.
- Ability to travel extensively to various investigative sites.
- Proficiency in Microsoft Office Suite and clinical trial management systems.
- Strong problem-solving and analytical abilities.
Preferred Qualifications
- Previous experience with a global clinical research organization (CRO).
- Master's degree or Ph.D. in a relevant scientific discipline.
- Certification as a Clinical Research Professional (CCRP) or equivalent.
- Experience across multiple therapeutic areas.
- Fluency in additional languages.
Perks & Benefits
- Comprehensive Global Relocation Package (housing assistance, travel expenses, visa support).
- Competitive salary and performance-based bonuses.
- Generous paid time off and holidays.
- Robust health, dental, and vision insurance plans.
- RRSP matching program.
- Professional development and continuing education opportunities.
- Employee wellness programs.
- Collaborative and inclusive work environment.
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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