Study Nurse Freelance

 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.The Study Nurse coordinates and manages clinical studies with drugs, medical devices and cosmetics as Study Nurse under the supervision of the Principal Investigator (PI) in cooperation with the TFS In-house Clinic study team according to the policies and Standard Operating Procedures of TFS and in compliance with Good Clinical Practice as well as with the national and international regulations for clinical studies and data protection  Key ResponsibilitiesStudy Set-up:- Complete feasibility questionnaires from Sponsors- Prepare and attend Pre-study visits- Complete the site qualification questionnaire for EC submission- Participate in the investigator meetings of the Sponsors- Plan and attend Site Initiation Visits- Support patient recruitment in collaboration with the investigatorsStudy Conduct according to the protocol-related tasks delegated by the PI:- Coordinate, prepare and conduct patients visits according to the study protocol and support the investigators also in screening activities- Conduct diagnostic tests such as vital signs, etc.- Collect and process biological samples- Manage laboratory shipping logistics - Dispense and administer the Investigational Medicinal Product to study participantsfollowing the instructions of the investigators- Manage the Drug Accountability including storage, preparation of the InvestigationalMedicinal Product- Main contact person for communication with study participants, CRAs and Sponsors- Manage patients reimbursements and investigator feesStudy project documentation:- Prepare and maintain patient files for source documentation- Capture Source Data in various electronic or paper-based Data Capture Systems- Resolve Data Queries in collaboration with the investigators- Maintain the Investigator Site Files- Assist in Serious Adverse Event reporting- Prepare, support and post-process monitoring visits and audits/inspections- Archive study documents Qualifications- Work Experience as Study Nurse (2 years ideally) - Excellent organizational skills, ability to prioritise and handle multiple competing priorities and timelines- Excellent verbal and written communication skills- Ability to work independently and in a team- Knowledge of the Good Clinical Practice- Very good command of written and spoken English- Good knowledge of MS Office- Willingness to travel on occasion What 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 patientsA 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 are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.