div>Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills.
- Responsible for the completeness of documents managed in the Trial Master Files (TMF); performs ongoing reviews of TMF to assure quality of the documentation files and compliance with SOPs and ICH GCP Guidelines.
The Senior Clinical Project Manager will provide operational expertise within the Research and Development function to ensure timely initiation, execution and reporting of clinical trials in accordance with ICH/GCP and all applicable requirements (including local regulations) to support licensure of products in the United States and global markets.
div>Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role in ensuring the integrity, accuracy, and completeness of clinical trial data, contributing to the successful development and regulatory approval of our products.
div>We are seeking a highly analytical and inquisitive Clinical Scientist to provide analytical support for a high-priority, Global Phase 2/3 pivotal program reporting to the Chief Medical Officer (CMO).
Compensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks.