About the Company
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to accelerating innovation and delivering exceptional outcomes for patients worldwide. With a strong global presence and a dedication to scientific advancement, IQVIA offers unparalleled opportunities for career growth and impact.
Job Description
We are seeking a dedicated and experienced Clinical Research Associate (CRA) to join our dynamic team in Maidstone, Kent. In this hybrid role, you will play a crucial part in the execution of clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements. This position offers an exciting opportunity to contribute to groundbreaking research that impacts global health, working within a supportive and collaborative environment.
Key Responsibilities
- Conduct pre-study, initiation, routine monitoring, and close-out visits for clinical sites.
- Ensure the safety and well-being of study participants and the integrity of clinical data.
- Verify that all research activities are conducted in accordance with the study protocol, GCP, and applicable regulatory requirements.
- Review and reconcile Case Report Forms (CRFs) against source documents.
- Manage site queries and ensure timely resolution.
- Provide training and support to site staff on study protocols and procedures.
- Prepare and submit regulatory documents as required.
- Maintain accurate and up-to-date documentation for all monitoring activities.
Required Skills
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of ICH-GCP guidelines and relevant regulatory requirements.
- Proven ability to monitor clinical trials across various therapeutic areas.
- Excellent written and verbal communication skills.
- Strong organizational and time management abilities.
- Proficiency in clinical trial management systems and Microsoft Office Suite.
- Ability to travel regularly to clinical sites.
Preferred Qualifications
- Bachelor's degree in a life science-related field.
- Experience with electronic data capture (EDC) systems.
- Previous experience in a global clinical research organization (CRO) setting.
- Certification as a Clinical Research Associate (e.g., CCRP).
Perks & Benefits
- Competitive salary and performance-based bonuses.
- Comprehensive health and dental insurance.
- Generous paid time off and holiday allowance.
- Opportunities for professional development and continuous learning.
- Retirement savings plan with company match.
- Employee assistance program.
- Hybrid work model promoting work-life balance.
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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