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 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.   Physical Requirements:   Frequently vertical and /or 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.   Frequent 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 moderately complex 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, relates sensitive information to diverse groups.   Ability to apply basic principles to solve conceptual issues.   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.