FREE ACCESS
5,000–10,000 jobs/day

See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Contributes to the selection of potential investigators
- In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance
- Trains, supports, and advises Investigators and site staff in study related matters
- Ensures the sites are inspection ready at all times
- Actively participates in Local Study Team (LST) meetings
- Drives performance at the sites
- Updates CTMS and other systems with data from study sites as per required timelines
- Performs monitoring visits (remote and onsite)
- Ensures data query resolution in a timely manner
- Supports/participates in regular QC checks performed by LSAD or delegate
- Ensures compliance with client ’s Code of Ethics, company policies and procedures
Requirements
What you’ll need- Bachelor degree in related discipline, preferably in life science, or equivalent qualification
- Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP
- Good knowledge of relevant local regulations
- Good medical knowledge and ability to learn relevant client’s Therapeutic Areas
- Basic understanding of the drug development process
- Good understanding of Clinical Study Management including monitoring, study drug handling and data management
- Excellent attention to details
- Good written and verbal communication skills
- Good collaboration and interpersonal skills
- Good negotiation skills
- Ability to travel nationally/internationally as Required
Benefits
Comp & perks- Paid time off
- Flexible work arrangements
- Professional development
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
monitoring visitsdata query resolutionstudy start-upregulatory maintenanceClinical Study Managementstudy drug handlingdata managementQC checksICH-GCPGMP/GDP
Soft Skills
attention to detailwritten communicationverbal communicationcollaborationinterpersonal skillsnegotiation skills
