Thermo Fisher Scientific·Austin, Texas
The Study Team Associate supports clinical operations by assisting with screening, study conduct, and data entry phases of trials. Key tasks include conducting informed consent sessions, coordinating participant visits, and performing administrative duties to support study management.
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.
Per Diem (as needed/no guaranteed hours); flexibility to cover all shifts as clinic operates 24/7; average availability requested ~29hrs/week
Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we collaborate with clients to define and develop clinical programs, reduce delays, and implement high-quality, cost-efficient clinical studies.
Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for supporting all study management roles within Clinical Operations. This entails tasks within the screening, study conduct and data entry phases of the trials. Inclusive of, but is not limited to, conducting a screening session to provide the Informed Consent session as delegated by the Principal Investigator, coordinating and performing tasks associated with checking in, checking out and conducting outpatient visits for participants actively enrolled in studies as well as performing a variety of team related procedures. Supports team members within their own study team as well as other study teams within the Clinical Operations department.
Fulfills all training expectations associated with tasks that support clinical trials within the study management roles
Serves as back up, when needed, for study primaries within the Enrollment, Coordinating and Data Entry positions.
Completes administrative tasks such as preparing, reviewing and verify source as well as coordinating management of supplies for upcoming visits.
Experience
Previous applicable experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
In some cases, a combination of appropriate education, training and/or directly related experience will be considered sufficient and equivalent for an individual to meet the requirements of the role.
Knowledge, Skills, Abilities
Demonstrated ability handling multiple responsibilities and completion of projects with overlapping prioritization.
Basic computer skills including knowledge of Microsoft Office and the ability to learn various programs and/or data management or electronic source systems.
Strong communication skills. Ability to clearly explain information to a wide variety of individuals.
Ability to work closely with multiple types of individuals in potentially difficult or uncomfortable settings.
Strong attention to detail with strong planning and organization capabilities to manage multiple tasks and multiple study groups at one time.
Effective time-management while demonstrating ability to communicate need for assistance.
Physical Requirements / Work Environment
Work is performed in an office or clinical environment.
Frequent long hours, weekends, and/or holidays.
Exposure to blood and biohazardous waste.
Be available by cell phone after hours.
Potential occasional travel required.
Market context
In Texas, per diem Study Team Associate roles are typically tied to clinical research settings where scheduling flexibility and dependable support are important. These positions can be competitive because employers often look for candidates who combine basic computer skills, clear communication, and the ability to manage multiple priorities in a clinical environment. Review the AI-summarized requirements and benefits on this platform to save time, then tailor your application to any patient-facing, scheduling, or administrative experience.
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