Travel Research Associate

Thermo Fisher Scientific•Atlanta, GA

8d•Hybrid

About The Position

Join us as a Travel 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.

Requirements

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.
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 computer skills, including proficiency in MS Office (Word, Excel, and PowerPoint) and basic understanding of clinical trial database systems
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
Strong analytical and data management skills to effectively analyze data/systems to ensure accuracy and efficiency

Responsibilities

Become a member of the traveling virtual site operations SWAT team and expected to travel 65 to 70% to site locations in Florida, Georgia and other neighboring states.
May perform Phlebotomy.
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.