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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Leads Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines.
- Coordinates the site selection process by identifying potential sites/investigators.
- Plans and coordinates applicable to local drug activities.
- Reviews monitoring visit reports and pro-actively advises the monitor(s) on study related matters.
- Proactively identifies risks and facilitates resolution of complex study problems and issues.
- Reports study progress/update to the Global Study Associate Director/ Global Study Team.
Requirements
What you’ll need- Minimum 3 years of experience in Development Operations (CRA, SrCRA) or other related fields (Medical Affairs-led or Academic-led studies).
- Good knowledge of international guidelines ICH GCP as well as relevant local regulations.
- Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality.
- Excellent project management skills.
- Excellent team building and interpersonal skills.
- Excellent organizational skills.
- Excellent verbal and written communication skills.
- Proficient in written and spoken English language required.
- Fluency in local language(s) required.
Benefits
Comp & perks- Flexible work arrangements
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Development OperationsClinical Research Associate (CRA)Senior Clinical Research Associate (SrCRA)Project Management
Soft Skills
LeadershipTeam BuildingInterpersonal SkillsOrganizational SkillsVerbal CommunicationWritten Communication
