Clinical Research Coordinator

Overview We are seeking a dedicated Clinical Research Coordinator to join our team. The ideal candidate will play a crucial role in managing and coordinating clinical trials, ensuring compliance with regulatory standards, and contributing to the advancement of medical research. Responsibilities - Coordinate and oversee clinical research studies from initiation to completion - Perform data collection, management, and analysis using statistical software - Conduct documentation review to ensure accuracy and compliance with protocols - Assist in blood sampling procedures and other clinical assessments - Manage regulatory compliance throughout the research process - Collaborate with healthcare professionals to support clinical development activities - Ensure adherence to Good Clinical Practice (GCP) guidelines Qualifications - Previous experience as a nurse or in a related healthcare field is preferred - Proficiency in data management and statistical software applications - Ability to analyze and interpret complex data sets accurately - Strong organizational skills with attention to detail - Knowledge of compliance management in clinical research settings - Familiarity with blood sampling techniques and clinical trial procedures - Understanding of Good Clinical Practice (GCP) guidelines - Excellent communication and interpersonal skills If you are passionate about contributing to groundbreaking medical research and possess the necessary skills and qualifications, we encourage you to apply for this rewarding opportunity as a Clinical Research Coordinator. Job Types: Contract, Temporary Pay: $28.22 - $30.00 per hour Expected hours: 40 per week Medical Specialty: Dermatology Gastroenterology Oncology Urology Schedule: 8 hour shift Day shift Monday to Friday Night shift Experience: Clinical research: 2 years (Required) Academic Medical Center: 2 years (Required) IRB: 2 years (Required) CRFs: 2 years (Required) Work Location: In person