Associate Clinical Research Associate
Descrizione dell'offerta
Start-up Associate / In-House CRA
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Italy | Full-time| Long-term Outsourcing Contract | Top Global Medical Devices Company
Are you ready to take the next step in your clinical research career?
We are looking for an experienced In-House CRA to join our team and support the planning and conduct of clinical studies for a leading international player in the medical devices industry.
This is a long-term, full-time outsourcing contract offering the chance to work on impactful projects directly embedded within the client’s team.
Key Responsibilities
Ensure regulatory and protocol compliance across assigned studies.
Support in the preparation of study materials (patient brochures, informed consent forms, presentations, reports).
Coordinate site start-up, maintenance, and vendor/committee oversight.
Collect essential documents, track data corrections, review adverse events & protocol deviations.
Assist in monitoring activities, audits, and resolution of findings.
Draft Serious Adverse Event narratives and process product complaints.
Act as a liaison between study management, field clinical personnel, and site staff.
Mentor and train less experienced clinical team members.
Requirements
✔ Bachelor’s degree in Life Sciences, Nursing, Medicine, Bioengineering, or related field.
✔ Minimum 2 years of clinical research experience (mandatory).
✔ Strong communication, organizational, and problem-solving skills.
✔ Ability to work both independently and collaboratively.
✔ Proficiency with MS Office and relevant clinical applications.
✔ Fluent in Italian and English (written & spoken).
What We Offer
✨ Full-time, long-term outsourcing contract with a top medical devices company.
✨ Opportunity to grow within a global and highly innovative environment.
&## ;
Italy | Full-time| Long-term Outsourcing Contract | Top Global Medical Devices Company
Are you ready to take the next step in your clinical research career?
We are looking for an experienced In-House CRA to join our team and support the planning and conduct of clinical studies for a leading international player in the medical devices industry.
This is a long-term, full-time outsourcing contract offering the chance to work on impactful projects directly embedded within the client’s team.
Key Responsibilities
Ensure regulatory and protocol compliance across assigned studies.
Support in the preparation of study materials (patient brochures, informed consent forms, presentations, reports).
Coordinate site start-up, maintenance, and vendor/committee oversight.
Collect essential documents, track data corrections, review adverse events & protocol deviations.
Assist in monitoring activities, audits, and resolution of findings.
Draft Serious Adverse Event narratives and process product complaints.
Act as a liaison between study management, field clinical personnel, and site staff.
Mentor and train less experienced clinical team members.
Requirements
✔ Bachelor’s degree in Life Sciences, Nursing, Medicine, Bioengineering, or related field.
✔ Minimum 2 years of clinical research experience (mandatory).
✔ Strong communication, organizational, and problem-solving skills.
✔ Ability to work both independently and collaboratively.
✔ Proficiency with MS Office and relevant clinical applications.
✔ Fluent in Italian and English (written & spoken).
What We Offer
✨ Full-time, long-term outsourcing contract with a top medical devices company.
✨ Opportunity to grow within a global and highly innovative environment.