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.CareersClinical Research AssociatePrivate Foundation Món Clínic BarcelonaBarcelonaKey ResponsibilitiesAct 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 InterfacesAll departments within the Operations area.EducationUniversity 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 RequirementsSolid understanding of Good Clinical Practice (GCP).Knowledge of the regulatory framework governing clinical studies.Understanding of data protection regulations applicable to clinical research.ExperienceMinimum 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 mentorshipwill be provided.Desirable experience in clinical investigations with medical devices.Desirable experience using electronic platforms, including e CTMS and e TMF.LanguagesSpanishAdvanced English level (spoken and written).Other RequirementsAbility and willingness to travel, both domestically and internationally.Core Competencies & SkillsKnowledge 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
📍 Barcelona