
Clinical Research Coordinator I with hands-on experience supporting complex study workflows, participant management, and regulatory documentation across academic and private research settings. Proficient in EDC systems, data entry and quality control, bio-specimen handling, and IRB support; known for strong regulatory compliance, patient communication, and time-sensitive coordination. Eager to expand research responsibilities, contribute to high-quality clinical trials, and continuously learn through collaborative, detail-focused work.
Experienced leader with strong background in guiding teams, managing complex projects, and achieving strategic objectives. Excels in developing efficient processes, ensuring high standards, and aligning efforts with organizational goals. Known for collaborative approach and commitment to excellence.