Freelance Senior Clinical Research Associate

Freelance Senior Clinical Research Associate2 days ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.About This RoleTFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey.Our expertise includes full service-capabilities, resourcing and functional service (FSP) solutions.As part of our SRS/FSP team, you will be dedicated to one sponsor.Please keep in mind that this is a 1 year contract Freelance opportunity for approximately 0.1 FTE -0.2 FTE.Key ResponsibilitiesMonitor clinical trials on-site and remotely in accordance with TFS/client SOPs, FDA regulations, and GCP/ICH guidelinesReview CRFs (paper or electronic) and subject source documentation for validity and accuracy; generate queries to resolve data issuesIdentify site problems or deficiencies and report them to management through trip reports, memos, and communication with the Project Manager or Lead CRAInitiate corrective actions as directed by the supervisorContribute to Ethics Committee/IRB application submissions and prepare required documentation in collaboration with the CTA and as directed by the Lead CRA/Project ManagerParticipate in contract handling and negotiation under direction of the Lead CRA/Project ManagerSet up the Investigator Site File (ISF) and Study Master File (SMF), or support the CTA in doing so, and distribute materials to investigational sitesCollaborate with the study team on SMF maintenanceOrder, ship, and reconcile clinical investigational supplies for study sites, if applicableCoordinate ordering and shipment of study supplies to sitesPrepare and submit status reports as directed by the Lead CRA/Project ManagerReview and support site staff in maintaining the SMFReview Informed Consent Forms for essential elements and protocol complianceUpdate CTMS with site and study informationAudit data in tables and text of clinical summaries (as applicable)Assist in preparing study documentation—such as CRF Completion Guidelines, patient diaries, and study participation cards—by reviewing for accuracy and completenessPrepare check requisitions for sponsor Project Manager approval, when applicableQualificationsBachelor's degree, preferably in life sciences or nursing, or equivalentMinimum of 2 years of experience working as a CRA (in oncology)Ability to work in a fast-paced environment with changing prioritiesUnderstanding of basic medical terminology and science related to assigned drugs and therapeutic areasSolid understanding of Good Clinical Practice (GCP) regulations and ICH guidelinesAbility to work independently and within a team/matrix organizationExcellent written and verbal communication skillsStrong organizational skillsAbility and willingness to travelWhat We OfferWe provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment.You'll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.A Bit More About UsOur journey began over 27 years ago in Sweden, in the city of Lund.As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future.Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decision-making at all levels of the organization and foster a culture of mutual respect and collaboration.Together we make a difference.Seniority levelMid-Senior levelEmployment typeContractJob functionResearch, Analyst, and Information TechnologyIndustriesPharmaceutical Manufacturing#J-*****-Ljbffr