Tech Stack
Google Cloud Platform
About the role
- Lead Local Study Team(s) at country level to deliver clinical studies
- Ensure that sites are identified, set up, initiated, monitored, and documentation archived
- Coordinate the site selection process and perform feasibility assessments
- Manage local drug activities and maintain study documentation
- Oversee monitoring activities from site activation through study closure
- Report study progress to the Global Study Associate Director
Requirements
- Minimum 3 years of experience in Development Operations (CRA, SrCRA) or other related fields
- Good knowledge of international guidelines ICH GCP as well as relevant local regulations
- Bachelor’s degree in related discipline, preferably in life science, or equivalent qualification
- Ability to travel nationally and internationally as required
- Integrity and high ethical standards
- Health insurance
- Opportunity for professional development
- Flexible work arrangements
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
Development OperationsClinical Research Associate (CRA)Senior Clinical Research Associate (SrCRA)Feasibility assessmentsSite selectionStudy documentation managementMonitoring activitiesStudy closure processes
Soft skills
IntegrityHigh ethical standardsCoordinationCommunication