readiness team in a timely and professional manner. Requirements: Bachelor's degree in a scientific discipline such as life... sciences, pharmacy, bioscience; advanced degree preferred. 5+ years of experience in regulatory affairs within the...
management, particularly in the oncology field. Requirements: Bachelor's degree in Life Sciences, Computer Science...
management, particularly in the oncology field. Requirements: Bachelor's degree in Life Sciences, Computer Science...
in a life science or technical discipline, preferably in engineering, bioengineering, biology, or chemistry. 2-5 years Medical...
communicate CMC regulatory strategies, risks and key issues throughout the life cycle in a timely manner to project teams...
standards (e.g., ICH-GCP, CDISC). Requirements: Bachelor's degree in a life science, health science, pharmacy, public health...
in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
, and management of the clinical study database throughout its life cycle, from CRF design, database development and testing...
programming experience in the life science industry and relevant bachelor's degree Must have recent NDA submissions experience...
standards (e.g., ICH-GCP, CDISC). Requirements: Bachelor's degree in a life science, health science, pharmacy, public health...
). Expertise in development, validation, and management of the clinical study database throughout its life cycle, from CRF design...
). Expertise in development, validation, and management of the clinical study database throughout its life cycle, from CRF design...
Job Description: The Sr. Product Quality Engineer will serve as a technical representative providing design quality expertise to a product development team. Responsible for maintaining a strong collaborative partnership with cross-functi...
Responsibilities: Lead clinical data management activities for pivotal trials in a dynamic environment. Collaborate with cross-functional teams to ensure high-quality data deliverables. Drive vendor management and oversee complex multi-...
Job Description: This position is Non-exempt. Hours over 40 will be paid at Time and a Half. The Sr. Product Quality Engineer will serve as a technical representative providing design quality expertise to a product development team. Resp...
Job Description: The Sr. Product Quality Engineer will serve as a technical representative providing design quality expertise to a product development team. Responsible for maintaining a strong collaborative partnership with cross-functi...
Responsibilities: In this critical role, you will lead regulatory strategies, product submissions, and a team of talented regulatory affairs professionals to drive timely product approvals and ensure ongoing regulatory compliance in key m...
Responsibilities: In this critical role, you will lead regulatory strategies, product submissions, and a team of talented regulatory affairs professionals to drive timely product approvals and ensure ongoing regulatory compliance in key m...
Responsibilities: Provides leadership/expertise in day-to-day statistical programming in support of ongoing projects. Develops and/or validates SAS programs to generate SDTM/ADaM datasets following industry standards, regulatory requirem...
Responsibilities: Participate in developing and maintaining clinical trial data and statistical programming standards to ensure the company standards are up to date and in line with pharmaceutical industry standards, conventions, and regu...