Ensure delivery of quality study strategy and design, understand the analysis and interpretation of data throughout the study
Lead or contribute, as appropriate, to the end to end delivery of clinical development activities which ensure consistency with the clinical development strategy for regulatory approvals
Understand the asset’s biological mechanism, clinical strategy, scientific interpretation of disease and target-based literature
Implement new business processes and strategies and may also proactively identify issues and propose strategies to manage implications and risks on clinical study
Requirements
Bachelor’s degree in Life Science or equivalent
2 or more years work experience in Pharma industry or relevant clinical trial experience
1 or more years Clinical trial and clinical research experience; running clinical trials in either the early or late phases
Experience working in a matrix management and large cross functional team environment
Experience generating clinical Protocols and ICFs
Experience working with data management and data cleaning of clinical data
Benefits
Health insurance
Retirement plans
Paid time off
Flexible work arrangements
Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical trial experienceclinical research experiencedata managementdata cleaningclinical protocolsinformed consent forms (ICFs)regulatory approvalsbiological mechanism understandingscientific interpretationtarget-based literature
Soft skills
leadershipcommunicationproblem-solvingstrategic thinkingcollaborationmatrix managementcross-functional teamworkorganizational skillsproactive identification of issuesrisk management