01 ago - Italia
ICON Strategic Solutions
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As Study Start Up Associate at ICON, you will be working within a large-scale, fast-paced environment, supporting the Study Start Up Team Lead in developing and execute the plan for country and site distribution.
What You Will Do
You will lead on site start-up and activation tasks requiring technical depth, with a focus on quality and continuous improvement.
Key Responsibilities Include
- Efficiently Drive Study Initiation: Conduct feasibility assessments, site identification, site contract negotiation, and other critical SSU activities.
- Empower Success through Specialized SSU Expertise: Provide expertise to Study Start Up team leads and project teams, providing valuable insights to drive success.
- Ensuring Regulatory Compliance: Prepare and coordinate submissions to regulatory, ethics, and other relevant bodies,
ensuring compliance with all necessary regulations and guidelines.
- Safeguarding Patient Welfare: Contribute to the development, finalization, and review of Master and Country Specific Subject Information Sheets/Informed Consent Forms, guaranteeing the highest standards of patient safety and informed consent.
Your Profile
You will have a strong foundation in site start-up and activation, with the experience to work independently and guide others.
Required Qualifications And Experience
- A Bachelor’s degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline.
- At least 3 years of experience or understanding of clinical study start-up requirements and activities, showing your expertise in the field.
- Fluency in the local language and English is essential, enabling you to effectively communicate and collaborate with international teams.
- Willing
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