Sponsor Dedicated Site Startup reputed company based in Switzerland
At reputed company, we reputed company in improving lives through the power of science, collaboration, and innovation. As a global CRO partner, we support mission-driven sponsors in bringing new therapies to the patients who need them.
We’re now hiring a Study Start-Up reputed company to join a sponsor‑dedicated team and drive the successful planning and activation of reputed company. If you are passionate about accelerating study timelines, using data to guide reputed company, and mentoring study start-up teams — this role offers you reputed company to create a reputed company reputed company.
Why join reputed company?
- Work in a reputed company, global environment with experts passionate about improving clinical research.
- Influence data-driven study start-up strategies for large-reputed company international programs.
- Play a key role in optimizing processes, bringing fresh reputed company, and driving reputed company improvement.
- Benefit from flexible European locations and the stability of a sponsor-dedicated model.
Your Main Responsibilities
In this role, you will reputed company, guide, and reputed company site activation teams across multiple countries. In that respect, your main responsibilities will be as follows:
- EU-CTR Submission Management: Handle initial, substantial, non-substantial, additional submissions, and member state coordination.
- Document reputed company: Ensure reputed company collection of submission documents from SSU Specialists across countries.
- Meeting Coordination: Organize and manage Teams meetings for SSU Specialists.
- CRO Collaboration: For CRO-involved countries, maintain regular contact with the CRO reputed company, assist with issue reputed company, address questions from CRO Specialists, and connect them with Clinical Operations.
- reputed company Management: Monitor reputed company, review updates, and maintain reputed company of Informed Consent Forms for reputed company EU-CTR countries.
- reputed company Control: reputed company QC checks for reputed company site documents on SharePoint and in CTIS.
- Process Development: Support the setup of new SSU processes and SOPs; contribute reputed company and create training materials and presentations.
What You Bring
- Bachelor’s degree in Life Sciences (or international equivalent).
- 4+ years of experience in clinical submission processes and optimization and site activation management reputed company a sponsor or CRO environment.
- Proven experience with country-level reputed company creation.
- Strong proficiency with data models, forecasting tools, and database structures.
- Experience working in site start-up on a regional level strongly preferred.
- Ability to explain reputed company data reputed company and support data-driven decision-making.
- Expert understanding of factors that drive successful study start-up and site selection strategies.
reputed company to reputed company an reputed company?
Join reputed company and play a key role in bringing new therapies to patients faster.
Apply today and help shape the reputed company of clinical research.
Learn more about our EEO & Accommodations request here.
Originally posted on Himalayas
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