Clinical Research Associate

OPIS; Barcelona; Sur place; EUR 45 000 - 55 000; Plein temps

Avantages offerts par ce poste

Additional benefits

Career growth opportunities

Résumé du poste

OPIS is hiring a Clinical Research Associate to manage and monitor multi-country trials, ensuring adherence to ICH-GCP and regulatory standards. You will oversee site selection, initiation, monitoring, and close-out activities, while safeguarding data quality and patient safety.

The role reports to the Clinical Project Manager and involves collaboration with sponsors, sites, and project teams. Requires a scientific degree and 2+ years’ CRA experience, with strong English and MS Office skills.

Qualifications

• Degree in a scientific field.
• Minimum 2 years’ CRA or clinical trial monitoring experience.
• Strong knowledge of ICH-GCP, ISO14155, and trial processes.
• Good English and Microsoft Office skills.

Responsabilités

• Identify, assess, and initiate investigational sites.
• Conduct feasibility, pre-study, initiation, monitoring, and close-out visits.
• Ensure compliance with protocols, SOPs, ICH-GCP, and regulatory requirements.
• Perform source data verification and ensure data accuracy and completeness.
• Monitor patient recruitment and support sites in meeting targets.
• Ensure proper reporting of adverse events and protocol deviations.
• Manage investigational product handling, storage, and accountability.
• Maintain study documentation (TMF/eTMF, Investigator Files).
• Write monitoring reports and follow-up communications.
• Collaborate with project teams, sponsors, and site staff.
• Support audits/inspections and mentor junior CRAs.

Connaissances

CRA experience

ICH-GCP knowledge

English language

Organizational skills

Communication skills

Teamwork

Formation

Degree in a scientific field

Outils

Microsoft Office

Description du poste

The Clinical Research Associate is responsible for managing and monitoring clinical trials to ensure they are conducted in compliance with study protocols, ICH-GCP, and applicable regulations. This includes site selection, initiation, monitoring, and close‑out activities, while ensuring data quality and patient safety. The role reports to the Clinical Project Manager.

Key Responsibilities

• Identify, assess, and initiate investigational sites
• Conduct feasibility, pre-study, initiation, monitoring, and close‑out visits
• Ensure compliance with protocols, SOPs, ICH-GCP, and regulatory requirements
• Perform source data verification and ensure data accuracy and completeness
• Monitor patient recruitment and support sites in meeting targets
• Ensure proper reporting of adverse events and protocol deviations
• Manage investigational product handling, storage, and accountability
• Maintain study documentation (TMF/eTMF, Investigator Files)
• Write monitoring reports and follow‑up communications
• Collaborate with project teams, sponsors, and site staff
• Support audits/inspections and mentor junior CRAs

Requirements

• Degree in a scientific field
• Minimum 2 years’ CRA or clinical trial monitoring experience (oncology and phase 1 studies highly desirable)
• Strong knowledge of ICH-GCP, ISO14155, and clinical trial processes
• Good English and Microsoft Office skills
• Strong organizational, communication, and problem‑solving abilities
• Ability to work independently and in a team

What we offer

• Salary up to EUR 50,000/annually based on experience
• Additional benefits
• Opportunity to develop career with an expanding company

Please read the information notice on the processing of personal data in the candidates information section of our company website.

Who we are

Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state‑of‑the‑art information technology solutions and innovative approaches to the increasing complexity and variety of current projects.

OPIS added value lies in its highly specialized professionals who can assist their clients using their deep know-how and experience to guarantee a top-quality level of Clinical Trial Management and ability to operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.) always contributing to our clients’ challenging achievements.