Build electronic health record query to support protocol design and feasibility process. Provide insights as to data quality/availability and feasibility of specific use cases to stakeholders and assess the reliability of methods used
Applicants should have Masters with greater than 15 years confirmed R&D experience or PhD with greater than 7 years experience in a life sciences field with a strong focus on molecular biology, protein design & purification, immunology, biotechnology and/or biochemistry.
Having IPQA experience in manufacturing & Packing of OSD. Proven experience in IPQA or a related field, with a strong understanding of pharmaceutical regulations and standards.
Develop and review Data Management procedures for clinical trials with sponsor companies and other departments; Establish/negotiate Data Management project timelines and ensure Data Management milestones are met