Senior Site Activation Specialist
2 tygodni temu
As a Senior Site Activation Specialist, you will play a key role in identifying and activating sites to the highest quality, ensuring patients on clinical trials have access to safe and effective medication.
Responsibilities- Review, establish, and agree on project planning and project timelines.
- Ensure monitoring measures are in place and implement contingency plans as needed.
- Negotiate and manage clinical trial agreements (CTA) with investigative sites and investigators.
- Work cross-functionally with Clinical and RSU Teams to support timely site start-up for the conduct of clinical trials.
- Review and negotiate budgets for CTA based on calculations provided by the Sponsor.
- Communicate and explain legal and budgetary issues to internal and external parties per project guidelines.
- Prepare and conclude amendments to CTA based on client-requested contract changes and study CTA guidelines.
- Appraise contracts for completeness and accuracy, ensuring adherence to department guidelines.
- Bachelor's Degree in Life Science or related field.
- Minimum 3 years' prior experience in life sciences or similar.
- Fluent/native language capabilities, including English.
- Ability to handle change and ambiguity.
- Ability to work on multiple projects.
About IQVIA
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
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