Employer Industry: Contract Research Organization

Why Consider this Job Opportunity:
- Competitive pay and benefits package
- Opportunity for career advancement and growth within the organization
- Chance to work on global clinical projects with a focus on delivering quality services
- Ability to work in a dynamic team environment
- Opportunity to gain experience in various therapeutic indications
- Flexibility to travel up to 65% (depending on project needs)

What to Expect (Job Responsibilities):
- Coordinate investigator/site feasibility and identification process, as well as study startup
- Monitor project timelines and patient enrollment, implementing corrective and preventive measures
- Review monitoring visit reports and ensure reporting compliance
- Manage Monitors in the query resolution process and coordinate safety information flow
- Perform clinical supplies management with vendors on a country and regional level

What is Required (Qualifications):
- Relevant educational background in Life Sciences or equivalent combination of education and experience
- Minimum of 5 years' site monitoring experience as a Lead Monitor in global clinical projects
- Strong experience in Oncology preferred
- Full working proficiency in English
- Proficiency in MS Office applications

How to Stand Out (Preferred Qualifications):
- Experience in CAR-T Therapy, Cell Therapy, Gene Therapy, Radiation Therapy, or Nuclear Medicine
- Valid driver's license (if applicable)

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