About the Company
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We create innovative solutions for our clients, helping them to accelerate medical innovation and improve healthcare outcomes. With a presence in over 100 countries, our mission is to drive healthcare forward by combining human science and data science.
Job Description
As a Clinical Research Associate (CRA) at IQVIA, you will play a pivotal role in the execution of clinical trials across various therapeutic areas. Based in Glasgow, this hybrid role requires a combination of on-site presence, remote work, and regular travel to investigational sites to monitor study progress, ensure adherence to protocols, and verify the accuracy of clinical data. You will be instrumental in safeguarding patient safety and data integrity, working closely with site staff, investigators, and the wider project team.
Key Responsibilities
- Conducting site selection, initiation, monitoring, and close-out visits in accordance with ICH-GCP guidelines, SOPs, and project-specific requirements.
- Ensuring the quality and integrity of clinical data through source document verification and review of case report forms.
- Managing investigator site files and essential documents to ensure compliance with regulatory standards.
- Providing ongoing training and support to investigational site staff on study protocols, procedures, and regulatory requirements.
- Identifying and resolving site-specific issues, including patient recruitment challenges and data discrepancies.
- Preparing and submitting visit reports and other required documentation in a timely and accurate manner.
- Collaborating effectively with project teams, clinical trial assistants, and other CRAs to achieve study milestones.
- Assisting with audit and inspection readiness activities as required.
Required Skills
- Bachelor's degree in a life science, nursing, or related health field.
- Minimum of 2 years of independent clinical monitoring experience in a CRO or pharmaceutical company.
- Thorough knowledge of ICH-GCP guidelines, applicable regulatory requirements, and clinical trial processes.
- Excellent communication, interpersonal, and presentation skills.
- Strong organizational skills and attention to detail.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to travel extensively within Scotland and potentially other parts of the UK as required.
Preferred Qualifications
- Master's degree or higher in a relevant scientific discipline.
- Experience across multiple therapeutic areas.
- Certification as a Clinical Research Associate (e.g., ACRP or SoCRA).
Perks & Benefits
- Competitive salary and performance-based bonus.
- Comprehensive health and dental insurance.
- Generous paid time off and public holidays.
- Company pension scheme.
- Opportunities for professional development and career growth.
- Access to a global network of industry experts and cutting-edge resources.
- Employee assistance program and wellness initiatives.
- Company car or car allowance.
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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