Job Title: Clinical Study Specialist Job Description A Clinical Study Specialist coordinates and oversees clinical operations of research projects. This role involves assessing and evaluating subjects/subject safety and conducting clinical research protocols in compliance with established clinical research organizational policies and Good Clinical Practices. The Clinical Study Specialist works under the general supervision of the Principal Investigator/Clinical Research Manager (PI/CRM) responsible for the clinical studies. Duties and Responsibilities: • Obtain and review records for potential research subjects; maintain study records of research subjects that include documentation of study procedures and progress, following guidelines set forth by the protocol sponsors. • Review recruited clinical study subjects for eligibility; schedule appointments and interviews, and evaluate potential subjects. • Instruct potential research subjects and responsible family members, nursing staff, and ancillary staff involved in research on the study procedures, treatments, and side effects. • Educate subjects concerning protocol and explain informed consent procedures, including obtaining subjects' written consent. • Evaluate and assist in developing subject education materials and give subjects and/or family members instruction on test article administration and other study information. • Perform nursing assessments and monitor subjects' progress during clinical studies and notify PI/CRM of any adverse events and serious adverse events, including evidence of unexpected side effects. • Perform initial interview during each subject visit and plan appropriate procedures according to the protocol. • If study requires instrumentation, set-up and verify instruments and conduct study with instruments. Assemble instrument data for study analysis. • Troubleshoot simple equipment or instrumentation issues if necessary. • Coordinate research activities and procedures for study subjects. • Complete case report forms for each study participant and document study data in subject study file. • Assess and document compliance of research subjects. • Provide orientation, information, training/cross-training, and assistance for new/existing personnel and research assistants, study staff to the research activities. Participate in staff meetings and in-service education. • Maintain adequate inventory of research supplies necessary for research activities. • Maintain exam rooms and laboratory. Hard Skills + Nursing + Clinical Research + Radiological Technologist Job Type This is a contract position with a duration of 30 Week(s), with possibility of extension based on performance. Work Site This is a fully on-site position in Neenah, Wisconsin. Work Environment Please note, hours could vary every single week as the schedule is based on business needs and not a set schedule. 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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.