Travel Research Associate

Responsibilities

• Join a virtual site operations SWAT team who is expected to travel 65 to 70% to different sites in the state and neighboring states
• May perform technical procedures running patient clinics including vital signs, 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

Benefits

• Resources needed to achieve individual career goals
• Collaboration and development as part of the everyday experience
• Glassdoor
• 3.5
• Thermo Fisher Scientific is a biotechnology and laboratory equipment company that provides a wide range of scientific products and services.
• Waltham, Massachusetts, USA
• https://www.thermofisher.com
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Qualifications

• 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
• 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 independently and with new site staff
• 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
• Strong analytical and data management skills to effectively analyze data/systems to ensure accuracy and efficiency
• Occasional drives to site locations with occasional travel both domestic and international
• Frequently stationary for 6-8 hours per day
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists
• Frequent mobility required
• Occasional crouching, stooping, bending and twisting of upper body and neck
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf
• Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences
• Frequently interacts with others to obtain or relate information to diverse groups
• Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration
• Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task
• Regular and consistent attendance
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).

Required skills

• Clinical Practices (GCP), FDA Regulations, Medical Terminology, Vital Signs Measurement, Microsoft Office, Clinical Trial Database Systems, Data Management

Experience

• 2+ years