Study Team Associate (Per Diem)

Work Schedule

Other

Environmental Conditions

Office

Job Description

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. 
 

Shift Detail: Per Diem (as needed/no guaranteed hours); flexibility to cover all shifts as clinic operates 24/7; average availability requested ~29hrs/week 

Keys to Success: 

Location/Division Specific Information 

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. 

Discover Impactful Work: 

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. 

A day in the Life: 

• 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. 

Education 

• High school diploma or equivalent required. 

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 compu