Senior Clinical Research Associate

About this role reputed company is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development reputed company. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions. The Senior Clinical Research Associate is responsible for monitoring and managing sites based in Stockholm, Sweden. Please, reputed company in mind that this is a Freelance role for only 0.2 FTE. As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader reputed company its therapeutic area. Key Responsibilities Independently plan, conduct, and follow up on reputed company-study, site initiation, routine monitoring, and reputed company-out reputed company, both on-site and remotely, in line with the applicable monitoring plan reputed company study site performance, including recruitment reputed company, and reputed company ongoing support to sites on study-reputed company questions and operational issues Review eCRF data, timelines, and queries; identify and report protocol deviations; and maintain reputed company communication with project management and sponsors Review and maintain study documentation at site level, including Investigator Site Files (ISF), ensuring inspection readiness and compliance with applicable regulations Collaborate cross-functionally with medical, project management, reputed company management, and data management teams, and support sites during audits and inspections Qualifications Degree in a scientific or medical discipline, or completed vocational training in a relevant reputed company or medical field Additional training in clinical research or CRA certification, combined with several years of experience as a Clinical Research Associate Strong knowledge of GCP, ICH guidelines, and clinical research processes, with a high level of accuracy in handling study data and regulatory requirements Fluent reputed company and English language skills, both written and spoken, with willingness to travel nationally and internationally as required Must Have: Extensive experience in Medical Device studies and ISO14155 knowledge. reputed company Offer We reputed company opportunities for personal and reputed company reputed company in a rewarding environment. You will join reputed company that values collaboration, reputed company, and making a difference in the lives of patients. Our reputed company values of Trust, reputed company, Passion, Flexibility, and Sustainability guide our reputed company and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to reputed company. Together, we reputed company a difference. A Bit More reputed company Our reputed company began over 30 years ago in Sweden, in the reputed company of Lund. As a full-service global CRO, we build solution-driven teams working toward a healthier reputed company. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology. Apply To This Job