Clinical Research Assistant

Insight Institute of Neuroscience & Neurosurgery (IINN) aims to advance, challenge, and revolutionize neurosciences and medicine through scientific research and advanced technology, driven by a passion to help others regardless of any obstacles and challenges that may lie ahead. Our integrated team of medical professionals does so through creative, innovative techniques and care principles developed because of our continuous pursuit to improve the field of medicine. Our integrated team works together to find solutions to both common and complex medical concerns to ensure more powerful, reliable results. Having multiple specialties "under one roof" Insight achieves its purpose in providing a comprehensive, collaborative approach to neuromusculoskeletal care and rehabilitation to ensure optimal results. Our singular focus is Patient Care Second to None!Job Summary:We are seeking competent, proactive, self-directed individuals with effective time management skills to assist our clinical research site. The Clinical Research Assistant will support the clinical research team at our Research Dearborn location. They will work under the direction of the Clinical Research Manager.Job Type:Full time (on-site, in-person)Monday to Friday, Full-time (8 hours), 8am - 5pm ESTAbility and willingness to commute between our research locations as needed per study tasksProfessional references may be required.Benefits for our Full Time Team Members:Comprehensive health, dental, and vision insurance coveragePaid time off, including vacation, holidays, and sick leave401K with Matching; offerings vested fully @ 3 months of employment paired with eligibility to contributeShort & Long Disability, and Life Term insurance, complementary of Full Time EmploymentAdditional Supplementary coverages offered @ employee's elections: Accident, Critical Illness, Hospital Indemnity, AD&D, etc.Duties and Responsibilities:Schedule visit appointments after coordination with relevant partiesCoordinate collection, processing and shipping of study specimensAssemble study kits for study visitsAttend and participate in study meetings, SIVs, monitoring visits and other sponsor and regulatory meetingsComplete Data Entry for studies both in sponsor EDC and CTMSEnsure all paper sources are filed and securely kept in the bindersAssist and work closely with the Clinical Research Coordinator and Clinical Research manager in executing and monitoring the overall clinical study to ensure compliance with protocolReport any adverse events according to the study protocolIdentify and assist in pre-screening potential subject leadsAssist in marketing the active trials in the communityActively meet with investigator and study team to discuss study progress/statusProvides administrative updates on enrollment and queries if anyOther duties as needed per assigned study protocolQualifications:Ability to demonstrate authorization to work in the U.S. for any employerBachelor's degree or equivalent training required via work experience or educationAt least one year of previous job-related experience preferredAbility to follow oral and written instructions and established policies and proceduresAbility to analyze and interpret dataAbility to finish tasks in a timely mannerAbility to maintain accuracy and consistencyAbility to maintain confidentialityAbility to work as an effective team memberKnowledge of medical terminologyAbility to function independently and manage their own time and work tasksDiligent, thorough in their tasks, and show their commitment to their jobInsight is an equal opportunity employer and values workplace diversity!