Clinical Research CoordinatorJob DescriptionA Clinical Research Coordinator is responsible for a variety of duties including the following: Overseeing the trouble-free running of clinical trials Performing patient consents to eligible study participants Managing budgets set aside for research Communicating with participants regarding study objectives Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules Liaising with laboratories regarding research findings Monitoring the study to ensure that it complies with protocols, is ethically conducted, and follows regulatory standards Maintaining research records of study activity, including case report forms, drug dispensation records, or other regulatory forms as per FDA guidelines Directing the collection, labeling, storage, and transport of all specimens Making sure that all equipment and supplies needed for the study are in stock and in good working orderHard Skills
1+ years clinical research coordinator experience
Enrollment, screening and consent experience
EDC experience
Bachelor's degree
Job TypeThis is a contract position with a duration of 5 Months.Work SiteThis is a fully on-site position in Bristol, TN.About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options.