CTA Job Opportunity at IQVIA | Apply Now
CTA job opportunities continue to grow across the global clinical research industry, and IQVIA is currently hiring a Clinical Trials Assistant II in Reading, United Kingdom. This hybrid role offers professionals with previous Clinical Trials Assistant experience the opportunity to support clinical research operations, collaborate with Local Trial Managers and Clinical Research Associates, and contribute to the successful delivery of clinical trials. If you are searching for IQVIA careers, a job in UK, or a rewarding life sciences job, this opportunity could be the perfect fit.
- Job Position:Â Clinical Trials Assistant II
- Company: IQVIA
- Location: Reading, United Kingdom
- Job ID: R1502172
About the Company
IQVIA careers attract professionals from around the world because IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company creates intelligent connections that help accelerate the development and commercialization of innovative medical treatments, ultimately improving patient outcomes and population health worldwide.
CTA Job Description
CTA job professionals at IQVIA play a vital role in supporting Local Trial Managers and Clinical Research Associates. The Clinical Trials Assistant II is responsible for tracking clinical trial progress, managing study data, overseeing budgets, supporting investigational product activities, handling correspondence, and performing various administrative tasks that contribute to the successful execution of clinical studies.
Candidates must be able to commute to the sponsor site for on-site work in Buckinghamshire. IQVIA is seeking professionals with previous CTA experience who can quickly integrate into ongoing clinical trial activities.
Qualifications
- Degree in Life Sciences or equivalent industry experience.
- Previous Clinical Trials Assistant (CTA) experience.
- Familiarity with Good Clinical Practice (GCP) and ICH guidelines.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Strong written and verbal communication skills in English.
- Excellent time management and organizational abilities.
- Strong collaboration and teamwork skills.
- Important Requirement: Job in UK applicants should note that this role is not eligible for UK visa sponsorship.
CTA Job – Key Responsibilities
- Maintain and update clinical systems and documentation, including the Trial Master File (TMF).
- Support the preparation, distribution, filing, and archiving of clinical documents and reports.
- Conduct periodic reviews of study files to ensure completeness and regulatory compliance.
- Assist with clinical trial supply logistics and tracking activities.
- Manage Case Report Forms (CRFs), queries, and clinical data flow.
- Serve as a central point of contact for project communications and documentation.
- Support Local Trial Managers and Clinical Research Associates throughout study execution.
- Monitor and track clinical trial progress and related operational activities.
CTA Job – Conclusion
CTA job seekers looking for a challenging and rewarding opportunity in clinical research should consider this Clinical Trials Assistant II position at IQVIA. With a strong global reputation, collaborative work environment, and meaningful contribution to healthcare innovation, this role represents an excellent opportunity for professionals seeking a job in UK within the growing life sciences job market.
