In-House Cra / Start-Up Associate

Oxford Global Resources; Chieti; In loco; EUR 40.000 - 50.000; Tempo pieno

Descrizione del lavoro

A leading global medical devices company in Italy is seeking an experienced In-House CRA to ensure compliance in clinical studies. This full-time position offers the opportunity to work independently and collaboratively on impactful projects directly within the client's team. Candidates must have a relevant degree and at least 2 years of clinical research experience, along with proficiency in Italian and English.

Servizi

Opportunity to grow within a global and highly innovative environment

Long-term outsourcing contract

Competenze

• Minimum 2 years of clinical research experience is mandatory.
• Ability to work both independently and collaboratively.

Mansioni

• Ensure regulatory and protocol compliance across assigned studies.
• Support in the preparation of study materials.
• Coordinate site start-up, maintenance, and vendor oversight.
• Collect essential documents and review adverse events.

Conoscenze

Communication skills

Organizational skills

Problem-solving skills

Fluency in Italian

Fluency in English

Formazione

Bachelor’s degree in Life Sciences, Nursing, Medicine, Bioengineering, or related field

Strumenti

MS Office

Clinical applications

Descrizione del lavoro

Start-up Associate / In-House CRA

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.

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.

Qualifications

• 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.