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 driving healthcare forward by providing unparalleled insights and delivering innovative solutions. With a presence in over 100 countries, IQVIA is at the forefront of human data science, offering a dynamic and challenging environment for professionals dedicated to making a difference. Our culture values collaboration, innovation, and continuous development, and we are proud to support global talent through comprehensive relocation packages.
Job Description
We are seeking a dedicated and experienced Clinical Research Associate (CRA) to join our esteemed team in Ipswich. This is an exceptional opportunity for CRAs looking to advance their careers within a global leader in clinical research. The successful candidate will be responsible for overseeing clinical trials at investigator sites, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements. This role is crucial for ensuring the integrity of clinical data and the safety of trial participants. We offer a comprehensive Global Relocation Package to support qualified international candidates in making a seamless transition to the UK, including assistance with visa processes, travel, and initial accommodation.
Key Responsibilities
- Conducting pre-study, initiation, routine monitoring, and close-out visits to clinical sites.
- Verifying that clinical trial data is accurately documented and reported, and that all necessary approvals are in place.
- Ensuring compliance with study protocols, standard operating procedures (SOPs), GCP, and regulatory requirements.
- Building and maintaining strong professional relationships with investigators and site staff.
- Reviewing and verifying source documents, case report forms (CRFs), and electronic data capture (EDC) systems.
- Providing training and support to site staff on study procedures and data collection.
- Participating in investigator meetings and other project-related training.
- Preparing visit reports and other necessary documentation in a timely and accurate manner.
- Identifying and resolving site-specific issues to ensure smooth trial progression.
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 understanding of clinical trial processes, GCP, and relevant regulatory guidelines.
- Excellent written and verbal communication skills.
- Strong organizational and time management abilities.
- Ability to work independently and as part of a team.
- Proficiency in Microsoft Office Suite.
- Valid driving license and ability to travel extensively as required.
Preferred Qualifications
- Master's degree or higher in a relevant scientific discipline.
- Experience in specific therapeutic areas such as oncology, cardiovascular, or neuroscience.
- Certification as a Clinical Research Associate (CCRA).
- Experience with various Electronic Data Capture (EDC) systems.
Perks & Benefits
- Comprehensive Global Relocation Package (including visa support, travel assistance, and initial accommodation support).
- Competitive annual salary.
- Performance-based bonus scheme.
- Private medical insurance.
- Pension scheme with company contributions.
- Generous paid time off and public holidays.
- Extensive career development and training opportunities.
- Access to a global network of industry experts.
- Employee assistance program and wellness initiatives.
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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