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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Build strong partnerships with clinical trial sites
- Manage assigned sites across Phase One to Phase Four trials
- Lead site initiation visits and ensure site teams are fully trained
- Conduct remote and on-site monitoring activities
- Evaluate site performance proactively and implement mitigation plans
- Drive early site engagement through feasibility activities
- Maintain complete and accurate study documentation
- Support inspection readiness through audit preparation
- Identify operational improvement opportunities and work with sites
Requirements
What you’ll need- Bachelor’s degree in a scientific, healthcare, or related field
- At least five years of clinical research experience
- Strong knowledge of clinical trial processes and ICH and GCP guidelines
- Understanding of global regulatory expectations
- Demonstrated ability to manage multiple study sites independently
- Strong communication and stakeholder management skills
- Strong analytical thinking and risk-based decision-making skills
- Willingness and ability to travel approximately fifty percent
Benefits
Comp & perks- competitive salary
- annual bonus
- life insurance
- retirement and wellbeing plans
- health insurance
- flexible working arrangements
- parental leave
- birthday day off
- employee recognition programs
- employee resource groups
- virtual self-development tools
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
clinical research experiencesite initiation visitsremote monitoringon-site monitoringstudy documentationaudit preparationrisk-based decision-making
Soft Skills
communication skillsstakeholder managementanalytical thinkingindependent managementpartnership building
