Assistant Clinical Research Coordinator

**Assistant Clinical Research Coordinator** **Company Overview** At DOCS Dermatology Group, we are not just one of the largest dermatology practices in the nation; we are a dedicated community passionate about skin health! With more than 200 providers across 20 practice brands and 100+ locations in 10 states, we’ve been transforming the lives of our patients for more than 40 years. Our mission is clear: to prioritize our patients with outstanding medical, surgical, and cosmetic dermatology services, all delivered in a friendly, convenient, and compassionate environment. **Summary** The Research Assistant will assist in the coordination and execution of clinical trials, ensuring compliance with regulatory requirements and maintaining the integrity of research data. **Job Responsibilities:** - Assist in the coordination of clinical research studies from initiation to completion. - Collect, record, and maintain accurate and complete research data in accordance with Good Clinical Practice (GCP) guidelines. - Coordinate with study sponsors, clinical trial sites, and other research team members. - Complete study-related tasks including vital signs, ECG, and collecting and processing laboratory samples. - Schedule and coordinate study visits, procedures, and laboratory tests as required by the protocol. - Assist in the preparation and maintenance of study-related documentation, including study binders, case report forms (CRFs), and study logs. - Assist with data entry, coding, and analysis as needed. - Participate in study meetings, trainings, and site visits as required. - Maintain strict confidentiality of participant information and research data. - Adhere to all applicable regulations, guidelines, and institutional policies governing clinical research. **Benefits** - Our benefits package includes medical, dental, and vision insurance, 401k matching, company paid life insurance, employee assistance program, and paid time off. **Minimum Qualifications:** - Bachelor’s degree in a relevant field (e.g., Life Sciences, Nursing, Public Health). - Previous experience in clinical research preferred. - Experience with phlebotomy/venipuncture preferred. - Familiarity with Good Clinical Practice (GCP) guidelines and regulatory requirements preferred. - Strong organizational skills and attention to detail. - Excellent communication and interpersonal skills. - Ability to work independently and collaboratively in a fast-paced environment. - Proficiency in Microsoft Office applications (Word, Excel, PowerPoint). - Flexibility to adapt to changing priorities and timelines. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status