Senior Clinical Operations Specialist

At the forefront of clinical research, we are seeking a Central Monitor II to play a pivotal role in ensuring the quality and integrity of trial data.

Key responsibilities include conducting thorough risk assessments for clinical studies, identifying potential issues, and developing mitigation strategies.

Additionally, the ideal candidate will possess strong analytical skills, with the ability to work independently and manage complex report review and issue escalation.

The selected individual will also have excellent written and spoken English skills, including strong grammar and scientific vocabulary.

Required qualifications include a Bachelor's Degree in a relevant field and minimum 2 years of experience in clinical monitoring or equivalent.

Responsibilities :

• Study Risk Assessment : Conduct detailed risk assessments for clinical studies to identify potential issues and develop mitigation strategies.
• Centralized Statistical Monitoring : Perform centralized statistical monitoring and data analysis on study data to detect anomalies, trends, and potential risks.
• RBQM Meetings : Participate in monthly RBQM meetings by reviewing study data, documenting findings, and coordinating data cleaning activities.
• Data Quality Assurance : Ensure the highest standards of data quality and integrity through proactive monitoring and timely interventions.
• Collaboration : Work closely with cross-functional teams to support proactive oversight and management.

We offer a competitive compensation package, with an estimated annual salary range of $180,000 to $360,000 , commensurate with experience.