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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Act as PAREXEL’s direct contact with assigned sites, assess and ensure overall integrity of study implementation and adherence to study protocol
- Build relationships with investigators and site staff
- Monitor and maintain compliance with ICH-GCP and applicable international and local regulations
- Evaluate site recruitment plan in collaboration with the site staff on an ongoing basis
- Conduct on-site visits for Qualification and Initiation visits
- Generate visit/contact report
- Evaluate overall compliance and performance of sites and site staff
- Ensure that assigned sites are audit and inspection ready
- Maintain a positive, results-orientated work environment, building partnerships and collaborative relationships
Requirements
What you’ll need- Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology
- Sound problem solving skills.
- Able to take initiative and work independently
- Advance presentation skills.
- Client focused approach to work.
- Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.
- Developing ability to work across cultures.
- Holds a driver’s license where required.
Benefits
Comp & perks- Health insurance
- 401(k) matching
- Flexible work hours
- Paid time off
- Professional development opportunities
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
site managementclinical researchclinical trials methodologyproblem solvingpresentation skills
Soft Skills
initiativeindependenceclient focusedcollaborative relationshipsresults-oriented
Certifications
driver's license
