Research Associate II

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join us as a Research Associate II - And utilize your expertise to support clinic operations, manage patient care workflows, assist with administrative tasks, ensure regulatory compliance, and enhance the efficiency and quality of clinical services. At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. What You’ll Do: • May perform technical procedures running patient clinics including vital signs, Fibroscan, height, weight, Electrocardiogram etc. Fully inform patients about the tests to be conducted and guides patients in the requirements of the trial. • May perform Phlebotomy tests. • Perform non-technical procedures, including urine collection, subject walks and safety monitoring. • Under the general supervision of a licensed physician, may conduct the education, evaluation, treatment and follow-up of sleep disorders for clinic patients by following sleep laboratory operating procedures, applying electrodes and sensors to ensure the collection of appropriate data of the sleep testing process. • Prepare and calibrate equipment for testing to ensure proper functioning. • Interact regularly with patients during study visits in order to perform study related procedures. • Undertake screening tests in accordance with protocol requirements. • Assist in the lab, sample processing and/or liaise with laboratories. • Manage and/or complete ordering of clinical supplies. • May assist with or oversee the maintenance of accurate freezer logs, specimen labelling and other documentation. • May take consent if permitted according to country regulations. • Report Quality Incidents and participate in the investigation and resolution. • Provide administrative support as needed. • Ensure adherence to COP’s, SOP’s, GCP and local regulations. • Provide training to new staff. • Note: Some tasks listed above only to be conducted as per country regulations and with relevant valid qualifications/ certification or supervision. Education and Experience: • Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: • Good medical terminology and ability to perform conducting of vital signs • Strong understanding of Good Clinical Practices (GCP), with ability to learn and maintain a good working knowledge of FDA regulations and company/client SOPs and WPDs • Strong organizational skills and flexibility to manage workload and meet changing timelines, handling multiple tasks efficiently and effectively • Thorough attention to detail to ensure accuracy and efficiency in data entry • Strong interpersonal/customer service skills, positive attitude and good oral and written communication • Capable of working in a team or independently • Strong English language and grammar skills • Strong