Research Associate III

Thermo Fisher Scientific•Atlanta, GA

3d•Onsite

About The Position

Join Thermo Fisher Scientific as a Research Associate III supporting clinical research operations and patient study visits. The role involves conducting clinical procedures, guiding patients through trial requirements, supporting sample processing and laboratory coordination, maintaining study documentation and supplies, and providing administrative support. Work must follow applicable clinical operating procedures, standard operating procedures, Good Clinical Practice (GCP), and local regulations. Certain duties require appropriate qualifications, certification, or supervision under country regulations. The position is performed in an office environment, with exposure to electrical office equipment and hazardous or toxic materials. Some personal protective equipment may be required. The role may involve occasional drives to site locations and occasional domestic or international travel. It requires regular interaction with patients and colleagues, independent work, sustained concentration, adaptability, and regular attendance.

Requirements

Bachelor's degree or equivalent, plus a relevant formal academic or vocational qualification.
Previous experience providing the knowledge, skills, and abilities to perform the role, comparable to 2 or more years; an appropriate combination of education, training, and directly related experience may be accepted in some cases.
Good medical terminology knowledge and ability to conduct vital-sign measurements.
Strong understanding of Good Clinical Practices and ability to learn and maintain working knowledge of FDA regulations and company/client SOPs and WPDs.
Strong organizational skills and flexibility to manage workload, changing timelines, and multiple tasks.
Thorough attention to detail for accurate and efficient data entry.
Strong interpersonal and customer-service skills, a positive attitude, and good oral and written communication.
Ability to work independently or as part of a team.
Strong English language and grammar skills.
Strong computer skills, including proficiency in MS Office (Word, Excel, and PowerPoint) and a basic understanding of clinical-trial database systems.
Strong analytical and data-management skills.
Ability to lift 40 lbs. without assistance, as listed under environmental conditions.
Ability to meet the role's physical and work demands, including frequent mobility, repetitive hand movements, occasional bending and twisting, and occasional lifting or carrying of objects up to 15–20 lbs.
Regular and consistent attendance.

Responsibilities

Perform technical procedures in patient clinics, which may include taking vital signs, height and weight, and conducting electrocardiograms; explain tests and trial requirements to patients.
Perform phlebotomy tests when appropriate.
Carry out non-technical procedures, including urine collection, subject walks, and safety monitoring.
Under the general supervision of a licensed physician, potentially conduct sleep-disorder education, evaluation, treatment, and follow-up by following sleep laboratory procedures and applying electrodes and sensors.
Interact with patients during study visits and perform study-related procedures.
Conduct screening tests in accordance with protocol requirements.
Assist in laboratory work and sample processing, and liaise with laboratories.
Manage or complete clinical-supply orders.
Assist with or oversee accurate freezer logs, specimen labeling, and other documentation.
Obtain informed consent when permitted by country regulations.
Report quality incidents and participate in their investigation and resolution.
Provide administrative support as needed.
Follow clinical operating procedures, standard operating procedures, Good Clinical Practice, and local regulations.
Train new staff.