Clinical Development Scientist

About the role

-Contributes, with appropriate oversight, to all relevant aspects of global clinical trial(s) activities to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s).

What you'll do

• Perform high quality clinical data review and identify clinical data insights through patient level review and trends analysis, supporting Interim Analysis
• Collaborate with relevant line functions to enhance the quality of clinical data review/insights with an emphasis on subject safety and eligibility, data integrity
• In conjunction with the relevant line functions, may contribute to Case Report Form (CRF) development, and support the implementation of data capture tools
• Contribute to and facilitate data review process improvements e.g. identification of delinquent/redundant reports and/or implementation of innovative data analysis…
• May contribute (in collaboration with relevant line functions) to the development of study-level documents, including clinical sections of key regulatory documents

What you need

• 3–4 yrs of experience
• Clinical research
• Pharmacovigilance
• M.Pharm or PhD or MBBS or BDS