We are looking for a detail-oriented and organized Clinical Data Manager (CDM) to join our expanding clinical research team. The ideal candidate will be a passionate advocate for data accuracy and integrity, ensuring the smooth and efficient flow of clinical trial data from collection to analysis. You will play a pivotal role in safeguarding the quality and compliance of our research and ultimately, the success of our clinical trials.

• Develop and implement clinical data management plans (CDMPs) for assigned clinical trials.

• Design and maintain electronic data capture (EDC) systems and databases.

• Oversee data collection, cleaning, verification, and coding activities.

• Manage data queries and discrepancies with clinical research sites.

• Perform data quality control audits and ensure adherence to GCP guidelines.

• Generate reports and summaries of clinical trial data.

• Collaborate with statisticians, clinical scientists, and other stakeholders.

• Monitor and manage clinical trial timelines and budgets.

• Stay up to date on regulatory requirements and best practices in clinical data management.