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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