Clinical Research Coordinator

Job Description A client of Insight Globalu2019s is seeking a Clinical Research Coordinator (CRC B/C) to support the dayu2011tou2011day operations of multiple investigatoru2011initiated and industryu2011sponsored dermatology clinical trials. On a daily basis, this individual will screen clinic schedules and medical records to identify eligible patients, conduct informed consent discussions, and coordinate protocolu2011required study visits and assessments. They will manage visit documentation, source documents, and regulatory binders; enter and review data in systems such as REDCap or sponsor EDC platforms; and ensure compliance with GCP, IRB, and institutional requirements. The coordinator will handle specimen collection and processing, monitor participants for adverse events, and support safety reporting as needed. This role requires independent management of 4u20135 active studies, regular communication with investigators, sponsors, and CROs, and close collaboration with a growing, teamu2011based clinical research unit. The position is ideal for someone looking to gain increased autonomy in clinical trials while remaining handsu2011on and patientu2011facing. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: Skills and Requirements 2u20136 years of clinical research experience (CRC B or CRC C level) Bacheloru2019s or Associateu2019s degree (or equivalent combination of education + experience) Handsu2011on experience consenting patients Patientu2011facing clinical research experience Independent coordination of industryu2011sponsored and/or investigatoru2011initiated studies Ability to review eligibility criteria, protocols, and source documents Working knowledge of GCP / ICH guidelines Experience with IRB submissions (initials, amendments, continuing reviews, AEs) Comfortable with specimen collection Penn Chart or Epic experience REDCap or sponsor EDC system experience Dermatology research experience (not required u2013 can be taught) Experience with drug / therapeutic studies Prior oversight of studies with minimal supervision Experience mentoring or supporting junior coordinators (CRC C level)

Created: 2026-04-09