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Join a leading Clinical Research Organization to support early-phase clinical trials in a dynamic, collaborative environment. As a Clinical Research Coordinator, you will oversee study operations, ensure compliance with protocols and regulations, and prioritize participant safety and data integrity.
Your responsibilities include leading study start-up activities, coordinating key events, reviewing protocols, collaborating with various teams, supporting client interactions, maintaining documentation, and supporting quality improvements.
Ideal candidates have a bachelor’s degree in life sciences or related fields, 3+ years of clinical research experience, and knowledge of GCP/ICH guidelines. Strong coordination, communication, and problem-solving skills are essential.
Work environments involve clinical/laboratory settings with exposure to biological fluids, occasional travel, and adherence to safety protocols. Physical requirements include working upright for extended periods and light lifting. The role demands adaptability in a fast-paced, technology-driven setting.
Benefits include comprehensive health coverage, 401(K), paid time off, recognition awards, and employee resource groups. This position offers opportunities for growth in a team-oriented, innovative environment.
