Project Associate Job

Project Associate (Germantown, MD) Design and develop comprehensive clinical research protocols by applying expertise in biology and regulatory standards, ensuring alignment with clinical objectives and compliance with applicable regulatory requirements. Prepare and review regulatory submissions, manage regulatory timelines, and coordinate cross-functional compliance activities to ensure accuracy and adherence to FDA and international regulations. Oversee clinical data management processes to ensure data integrity and accuracy, establish data collection and documentation standards for audit readiness, and serve as a liaison between project management and scientific teams while preparing and presenting reports for stakeholder updates. 40 hours/week, Master’s degree in Biology / Biological Engineering or related required. Resume to KCRN Research, Inc. Attn: Hyungjoo Lee, 12311 Middlebrook Road STE 200, Germantown, MD 20874

Master’s degree in Biology / Biological Engineering or related required.