Clinical Operations Associate

Job Title: Clinical Operations Associate Type: Contract Location: New Jersey Experience: 0-2 years Job Summary: We are seeking a motivated Clinical Operations Associate to support clinical trial planning, coordination, and documentation activities in pharmaceutical, biotechnology, and medical device organizations. The candidate will assist in managing study records, tracking clinical trial progress, and coordinating with cross-functional research teams. Key Responsibilities: Assist in coordinating clinical trial activities and study timelines. Maintain clinical study documentation and essential records. Support clinical site activation and study startup activities. Track patient recruitment and enrollment progress. Assist in preparing clinical study reports and status updates. Coordinate with investigators, clinical research teams, and study sites. Maintain Trial Master File (TMF) documentation. Follow ICH-GCP guidelines and applicable regulatory requirements. Skills Required: Basic understanding of clinical research and trial operations. Knowledge of clinical documentation and study protocols. Strong organizational and communication skills. Attention to detail and time management abilities. Proficiency in Microsoft Word and Excel. Preferred: Internship or academic project experience in clinical research. Familiarity with CTMS, EDC, or eTMF platforms. #J-18808-Ljbffr United Consulting Hub