Careers

Clinical Research Associate

Private Foundation Món Clínic Barcelona

Barcelona

Key Responsibilities

- Act as the main point of contact and support for the assigned investigational sites.

- Prepare, conduct, and report remote and onsite monitoring visits in accordance with the Monitoring Plan and applicable SOPs.

- Assess investigational site performance and ensure compliance with study protocol, GCP, and regulatory requirements.

- Perform all required activities during monitoring visits according to internal and/or sponsor procedures.

- Document and track the management of issues and deviations identified during and between site visits.

- Support investigational site staff in the resolution of issues/deviations and the development of Corrective and Preventive Action (CAPA) plans.

- Collaborate with Biometry, Regulatory Affairs, and Safety departments to obtain necessary site documentation.

Key Interfaces

- All departments within the Operations area.

Education

- University degree in Medicine, Biology, Biochemistry, Pharmacy, Nursing, Psychology, Chemistry, or other life science fields.

- Master’s degree in Clinical Study Monitoring or an equivalent qualification.

Training Requirements

- Solid understanding of Good Clinical Practice (GCP).

- Knowledge of the regulatory framework governing clinical studies.





- Understanding of data protection regulations applicable to clinical research.

Experience

- Minimum 1 year of experience in a similar role within clinical trials or internship experience in clinical research.

- Candidates with strong interest in clinical trials will also be considered; training and mentorship will be provided.

- Desirable experience in clinical investigations with medical devices.

- Desirable experience using electronic platforms, including eCTMS and eTMF.

Languages

- Spanish

- Advanced English level (spoken and written).

Other Requirements

- Ability and willingness to travel, both domestically and internationally.

Core Competencies &

Skills

- Knowledge of established quality standards and ability to follow internal instructions.

- Proactive attitude with a willingness to contribute to continuous improvement.

- Familiarity with cloud-based IT platforms and digital tools.

- Strong communication, reporting, and interpersonal skills.

- Comfortable working within multidisciplinary teams.

- Excellent organizational skills, independence, and strong time-management abilities.

- Effective active listening and negotiation capabilities.

- Rigorous, detail-oriented, and problem-solving oriented.

- Sound decision-making and ability to manage complex situations.

📌 Clinical Research Associate (Barcelona)
🏢 Barcelona Clinical Coordinating Center (BCCC)
📍 Barcelona