management, particularly in the oncology field. Requirements: Bachelor's degree in Life Sciences, Computer Science...
assessment and guidance on CMC-related change controls, deviations, and investigations throughout the product life cycle...
in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
in a life science or technical discipline, preferably in engineering, bioengineering, biology, or chemistry. 2-5 years Medical...
Job Description: Conducting oversight of vendors who identify and collect adverse event and product quality complaint information and complete in-take of Pharmacovigilance safety and product complaint reports in Client's Systems. Conduct...
Roles & Responsibilities: Good at ISO standards (ISO 14001, ISO 9001, ISO 45001). Experience in interacting with Customer to understand the quality issues and solve them. Shop floor experience on quality issues and providing solutions. ...
Responsibilities: Perform data management activities on both Electronic Data Capture (EDC) and paper studies. Responsible for the design and development of Case Report Forms (CRF) in collaboration with CRAs or Clinical Project/Program Ma...
Responsibilities: Leads all DM lifecycle activities, from study start-up, maintenance, database lock and close-out. Independently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CR...
Responsibilities: Position leads complex studies in study design, statistical analysis and interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision ...