Senior Clinical Research Associate

JR Italy; Chieti; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading medical device company in Chieti is seeking a Senior Clinical Research Associate. You will be responsible for conducting monitoring visits, ensuring compliance with regulatory standards, and supporting training for new staff. The ideal candidate has at least 5 years of CRA experience and a Bachelor’s degree in life sciences. A strong background in ICH/GCP guidelines is essential.

Competenze

• Minimum 5 years of CRA experience in medical device or pharmaceutical industry.
• Strong knowledge of MDR, ISO 14155, ICH/GCP guidelines.

Mansioni

• Conduct monitoring visits according to plans and procedures.
• Coordinate with research staff for site visits and evaluations.
• Ensure compliance and quality of site practices.

Conoscenze

Monitoring

Communication

Training

Formazione

Bachelor’s degree in life sciences

Descrizione del lavoro

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Senior Clinical Research Associate, Chieti

Client: Teleflex

Location: Chieti, Italy

Job Category: Other

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EU work permit required: Yes

Job Reference:

8556790222002585600337164

Job Views:

2

Posted:

27.08.2025

Expiry Date:

11.10.2025

Job Description:

POSITION SUMMARY: The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO 14155, ICH/GCP guidelines, Teleflex procedures, and IRB/EC policies). They evaluate data accuracy and subject safety, identify issues, present findings, and communicate with the study team. The Senior CRA should have at least 5 years of experience in clinical trial monitoring and assist with training and development of monitoring tools.

CULTURE: Teleflex emphasizes Customer Experience, Continuous Improvement, and adherence to company Values. Employees are expected to demonstrate professionalism, ethics, and effective cross-functional collaboration.

PRINCIPAL RESPONSIBILITIES:

• Conduct monitoring visits according to plans and procedures.
• Coordinate with research staff for site visits and evaluations.
• Ensure compliance and quality of site practices.
• Prepare for visits, document findings, and provide training as needed.
• Ensure regulatory compliance and proper documentation.
• Support safety reporting and regulatory submissions.
• Assist in training new staff and conducting audits.
• Participate in study team activities and maintain proper documentation.

EDUCATION / EXPERIENCE REQUIREMENTS:

• Bachelor’s degree in life sciences, nursing, or related fields.
• Minimum 5 years of CRA experience in medical device or pharmaceutical industry.
• Knowledge of vascular interventional therapies is a plus.

SPECIALIZED SKILLS & OTHER REQUIREMENTS:

• Strong knowledge of MDR, ISO 14155, ICH/GCP guidelines.
• Excellent monitoring, training, and communication skills.
• Ability to work independently and manage time effectively.