STUDY COORDINATOR

Job Title: Clinical Study CoordinatorLocation: Barcelona, Spain (Hybrid: 4 days in the office, 1 day remote)Experience Required: 1-3 years in clinical trials managementLanguages Required: English & Spanish (Fluent)About the Role:We are working with one of our key clients, a leading company in the healthcare industry, to find a talented Clinical Study Coordinator to join their team in Barcelona. This is a fantastic opportunity for an experienced clinical professional who is eager to contribute to the management of multiple clinical trials in a dynamic, fast-paced environment.As a Clinical Study Coordinator, you will be responsible for overseeing the day-to-day operations of clinical trials, working closely with internal and external stakeholders to ensure successful study execution, and helping to maintain the highest standards of compliance and quality.Key Responsibilities:Coordinate the execution of 4-5 clinical trials simultaneously, ensuring all deliverables are met within timelines.Act as the primary point of contact for site staff, investigators, and vendors involved in the clinical trials.Oversee the preparation, distribution, and collection of study materials, ensuring accuracy and compliance with trial protocols.Monitor study progress, track milestones, and report on trial status to internal and external stakeholders.Maintain study documentation, ensuring compliance with Good Clinical Practice (GCP), regulatory guidelines, and company SOPs.Support the Clinical Project Manager in managing budgets, timelines, and resource allocation for studies.Review and assist with site recruitment and retention strategies to ensure successful study enrollment.Assist with site monitoring visits, identifying and resolving issues in real-time to minimize study risks.Ensure that all clinical data is accurate and in compliance with ethical standards and regulatory requirements.Requirements:1-3 years of experience in clinical study coordination, clinical trial management, or as a Clinical Product Manager in a CRO, pharmaceutical, or medical device company.Proven experience managing 4-5 clinical trials concurrently.Strong understanding of clinical trial protocols, GCP, and regulatory requirements.Ability to handle multiple tasks simultaneously and work under pressure.Excellent organizational, communication, and problem-solving skills.Proficiency in both English and Spanish, with excellent written and verbal communication skills in both languages.Bachelor's degree in Life Sciences, Medicine, Nursing, or related field preferred.Preferred Qualifications:Experience in both clinical trials and product management within the healthcare industry.Knowledge of clinical trial management software (e.g., EDC, CTMS).What We Offer:Competitive salary and benefits package.Opportunities for career development and growth.A dynamic and collaborative work environment with a hybrid work model (4 days in-office, 1 day remote).If you have the required experience and are looking to take the next step in your clinical trials career, we’d love to hear from you! Apply now to be considered for this exciting opportunity with one of our esteemed clients.How to Apply:Please submit your resume and cover letter via LinkedIn