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ATS Keywords
Tailor your resumeApplicant 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)Project Management
Soft Skills
LeadershipTeam BuildingInterpersonal SkillsOrganizational SkillsVerbal CommunicationWritten Communication
Industry Keywords
Clinical TrialsICH GCPLocal RegulationsSite SelectionRisk Management
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
