At a Glance
- Tasks: Support regulatory submissions and activate sites for clinical trials.
- Company: Join IQVIA, a leader in healthcare data and analytics.
- Benefits: Flexible remote work, competitive salary, and career development opportunities.
- Other info: Collaborative environment with opportunities to grow your career.
- Why this job: Make a difference in clinical trials and contribute to groundbreaking research.
- Qualifications: Strong organisational skills and attention to detail required.
The predicted salary is between 35000 - 45000 £ per year.
IQVIA is seeking a Site Activation Coordinator to support regulatory submissions, feasibility assessments and activation of investigative sites for clinical trials.
You will work with the Site Activation Manager and cross-functional teams to ensure accurate documentation and timely delivery.
The role involves maintaining project plans, tracking documents, and coordinating with sites to complete questionnaires, CDAs, ethics submissions, and Investigator Packs.
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Remote Site Activation Specialist – Clinical Trials (UK) in Reading employer: IQVIA
IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.
