Marta Crespo Sánchez Email & Phone Number

Clinical Research Associate | Ensuring Excellence in Research and Patient Safety | NAMSAAs a dedicated Clinical Research Associate, I am committed to facilitating the successful implementation of clinical trials and ensuring the highest standards of research integrity and patient safety. With a deep understanding of regulatory requirements and industry guidelines, I specialize in overseeing and coordinating all aspects of clinical trial operations in medical devices.Key Skills:- Relationship Building: foster strong relationships with key stakeholders, including investigators, study coordinators, and ethics committees, to ensure effective collaboration and seamless trial execution.- Site Management: conduct thorough site evaluations, initiate site activation, and provide ongoing support and training to investigators and study coordinators.- Data Management: monitor data collection, verification, and quality control processes to ensure accurate and reliable trial results.- Trial Oversight: expertly manage the execution of clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements.- Compliance Assurance: Perform regular site visits and audits to ensure protocol compliance, source document verification, adverse event reporting, and investigational product accountability.Experience:-Demonstrated experience in monitoring clinical trials with medical devices across diverse therapeutic areas, adhering to industry best practices, and maintaining regulatory compliance all over Europe.-Excellent communication and interpersonal skills, enabling effective collaboration with multidisciplinary teams and stakeholders.-Proven ability to identify and address potential risks and issues proactively, ensuring timely resolution and minimizing impact on trial timelines.-Demonstrated experience in monitoring clinical trials across diverse therapeutic areas, adhering to industry best practices, and maintaining regulatory compliance.-Detail-oriented and analytical mindset, with a strong ability to interpret and analyze complex clinical trial data.