Principal Clinical Scientist

Job Description

As a Principal Clinical Scientist, your responsibilities include: * Leading the implementation of CSAI services according to the study scope of work on assigned project teams. * Serving as a scientific resource for project teams, focusing on data capture, review, and cleaning. * Supporting the development and implementation of process flow for integrated, cross-functional data cleaning. * Managing the overall data cleaning process to support interim and final data deliverables. * Managing Medical Monitor review of subject data. * Providing protocol review from a scientific operational perspective. * Offering scientific clinical input to Data Management for eCRF specifications and study documentation. * Supporting cross-functional departmental communication on data capture and review trends. * Identifying and managing study risks and deficiencies. * Supporting Project and Financial Management with monthly invoicing and variance management. * Collaborating with CSAI management to address resource needs. * Overseeing the development and maintenance of CSAI project-related plans and trackers. * Ensuring eTMF documentation is maintained as per study plans and SOPs. * Conducting scientific data review using programmed outputs. * Issuing and resolving queries in EDC systems. * Providing status updates on CSAI data review findings. * Managing the development and UAT of CSAI programmed outputs. * Providing study-specific training for CSAI Scientists and project teams. * Participating in internal and external team meetings and presentations. * Supporting data-related committees and meetings. * Reviewing TLFs and clinical study reports. * Participating in the interview process for CSAI candidates. * Supporting business development activities. * Promoting Precision’s high-quality and ethical image. * Developing and reviewing SOPs. * Presenting departmental trainings. * Contributing to company and CSAI process improvement initiatives.

Qualifications

1. Bachelor’s degree or equivalent in science or health-related discipline. 2. Minimum of 8 years of clinical research experience. 3. Minimum of 1 year of leadership experience. 4. Experience with electronic data capture systems. 5. Proficiency in Microsoft Office Products. 6. Excellent communication and interpersonal skills. 7. Excellent organization skills and attention to detail. 8. Professional use of the English language. 9. Ability to travel domestically and internationally.

Benefits

- Health insurance - Retirement plans - Paid time off - Flexible work arrangements - Professional development