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Role Summary:
The Director of Clinical Quality Assurance is responsible for leading Good Clinical Practice (GCP) Quality Assurance (QA) and serves as the GCP Quality representative for clinical study teams. This leader is skilled at building GCP processes and has in-depth knowledge of current GCP practices. This individual is the subject matter expert in GCP, is responsible for developing standards and partnering with Clinical Operations, Regulatory, Biostatistics, Safety, Medical Affairs, and other functions to establish and document risk based GCP processes and procedures. This role ensures compliance with applicable regulations with regards to sponsor oversight of Dyne’s clinical programs. This role is responsible for continuing to build out the quality infrastructure and evaluate, identify, and reduce compliance risk by contributing to the development and maintenance of efficient and effective clinical quality procedures to achieve the highest level of data quality and integrity.
This is a full-time position based in Waltham, MA without the possibility of being remote and requires ~25% travel.
Primary Responsibilities Include:
Educational and Skills Requirements
#LI-Onsite
Full Time
$118k-147k (estimate)
03/15/2024
07/10/2024
dyne-tx.com
Waltham, MA
<25
The following is the career advancement route for Director, Clinical Quality Assurance positions, which can be used as a reference in future career path planning. As a Director, Clinical Quality Assurance, it can be promoted into senior positions as a Quality Assurance Director- Healthcare that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Director, Clinical Quality Assurance. You can explore the career advancement for a Director, Clinical Quality Assurance below and select your interested title to get hiring information.