Employer Industry: Clinical Research

Why consider this job opportunity:
- Opportunity for career advancement and growth within a rapidly expanding organization
- Work remotely or from the office, providing flexibility in your work environment
- Engage in meaningful work that impacts the lives of patients through clinical trials
- Competitive salary and benefits package
- Collaborative work culture focused on employee well-being and development

What to Expect (Job Responsibilities):
- Conduct and report all types of onsite monitoring visits to ensure compliance with study protocols
- Manage site communication and oversee study activities, timelines, and schedules at the country level
- Perform CRF review, source document verification, and query resolution
- Participate in feasibility research and support the regulatory team with study submissions
- Supervise quality control efforts, including compliance monitoring and report reviews

What is Required (Qualifications):
- College/University degree in Life Sciences or equivalent combination of education, training, and experience
- Minimum of 5 years of independent on-site monitoring experience in the USA
- Experience in all types of monitoring visits in Phase II and/or III clinical trials
- Proven background in monitoring Oncology and/or Hemophilia trials
- Full working proficiency in English and proficiency in MS Office applications

How to Stand Out (Preferred Qualifications):
- Experience as a Lead/Senior Monitor in clinical research projects
- Strong communication, collaboration, and problem-solving skills
- Ability to plan and multitask effectively in a dynamic team environment
- Valid driver’s license (if applicable)

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