Clinical Research Coordinator

About this role

• **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** We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our growing team.
• The ideal candidate will play a crucial role in the successful execution of clinical research studies, ensuring compliance with protocols, regulations, and ethical standards.
• This is an excellent opportunity for an individual who is passionate about contributing to the advancement of medical science and patient care.
• **Job Responsibilities:** * Coordinate and manage various aspects of clinical research studies, including participant recruitment, informed consent, and data collection.
• * Collaborate with principal investigators, physicians, and other healthcare professionals to ensure smooth study operations.
• * Maintain accurate and organized study documentation, ensuring compliance with regulatory requirements.
• * Schedule study visits, manage participant appointments, and monitor their progress throughout the study.
• * Assist with the preparation and submission of regulatory documents to relevant authorities and ethics committees.
• * Collect, record, and manage study data with meticulous attention to detail.
• * Monitor participant safety and report any adverse events according to established protocols.
• * Conduct study-related assessments and measurements as required.
• * Prepare and contribute to study reports, presentations, and publications.
• * Maintain effective communication with study sponsors, participants, and interdisciplinary team members.
• * Stay up-to-date with relevant regulations, guidelines, and best practices in 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 related field (e.g., life sciences, nursing, healthcare) is preferred.
• * At least 3 years of experience as a clinical research coordinator or in a related role.
• * Experience with study start-up, contract and budget negotiations, and site regulatory submissions is preferred.
• * Strong organizational skills and the ability to manage multiple tasks concurrently.
• * Excellent interpersonal and communication skills.
• * Proficiency in using electronic data capture systems and MS Office suite.
• * Detail-oriented mindset with a commitment to accuracy and precision.
• * Ability to work independently and as part of a team in a fast-paced environment.
• 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

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