The Program Data Management Lead is responsible for leadership and overall strategic management of Programs in Clinical... Responsible for the overall success of the studies within a program(s) for Clinical Data Management (CDM). Maintains an overview...
landscape, assessing regulatory risk, and developing global filing strategies. Co-lead marketing application submission teams... synopses and protocols. Contribute in cross-functional rapid response teams to respond to Clinical Trial Application (CTA...
landscape, assessing regulatory risk, and developing global filing strategies. Co-lead marketing application submission teams... synopses and protocols. Contribute in cross-functional rapid response teams to respond to Clinical Trial Application (CTA...
across all full development / life cycle management assets and geographies. Key Words Scientific Writing, Medical Writer..., Regulatory and Safety Documentation, Protocol Development, ICH CTD Documentation Key Responsibilities Author complex clinical...
Parexel is currently seeking a Local Study Associate Director (Clinical Operations Leader) to join us in the UK.... You will be assigned to one of our key sponsors in the region. Working as a Local Study Associate Director (LSAD) at Parexel FSP offers...