Responsibilities · Lead the design, development, implementation, and execution of test scripts/test plans to identify software problems and their causes. · Coordinate and execute performance and functional testing associated with multip...
We need a BA to help elicit requirements from the clinical and regulatory stakeholders for system configuration and deployment. IRT is currently being deployed. SAS and eTMF are both in discovery phases but will kick off in next 30-60 days...
Responsibilities: Working knowledge of SAS® for production of datasets and tables, listings, and figures (TLFs) Develop, maintain, and produce statistical programs used in creating mapped datasets, analysis datasets, TLFs. Prepare stat...
The purpose of Business Development Manager is to Hunt new clients in US market and Sale the recruitment services. The role is coupled with Hands on Recruitment sales. The focus of the role is to identify the clients need and meet the requi...
SUMMARY OF POSITION The Associate, Regulatory Labeling prepares, reviews and submits to his/her manager high-quality regulatory labeling submissions intended for the FDA within company timelines and in accordance with regulatory guidelines...
We are seeking an experienced and dynamic Lifesciences Headhunter to join our team in Princeton, NJ. As a key member of our team, you will be responsible for identifying and attracting top talent in the life-sciences industry, helping our c...
SUMMARY OF POSITION Independently authors, compiles, reviews, schedules, and submits high-quality regulatory submissions in adherence with technical document standards that are fully compliant with FDA and ICH requirements within company t...
SUMMARY OF POSITION Manages team and leads Regulatory Associates and/or Senior Regulatory Associates in regulatory activities associated with planning, authoring, compiling and submitting highest-quality regulatory submissions to the FDA w...