Employer Industry: Contract Research Organization

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Competitive salary with potential for bonuses
- Gain experience across a variety of therapeutic indications
- Supportive and collaborative work environment
- Chance to make a significant impact on clinical study outcomes
- Travel opportunities up to 75% for site visits

What to Expect (Job Responsibilities):
- Act as the main line of communication between the project team, sponsor, and the site
- Prepare, conduct, and report site selection, initiation, routine monitoring, and close-out visits
- Ensure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations
- Conduct project-specific training of site investigators
- Review essential study documents and reconcile study Investigator Site File (ISF) / TMF at site level

What is Required (Qualifications):
- College/University degree in Life Sciences or equivalent combination of education, training, and experience
- Minimum 2 years of independent on-site monitoring experience
- Experience in all types of monitoring visits, in phases I-III
- Full working proficiency in English
- Ability to travel up to 75%

How to Stand Out (Preferred Qualifications):
- Experience in Oncology and GI/GU
- Proficiency in MS Office applications
- Strong communication, collaboration, and problem-solving skills
- Ability to plan and multitask in a dynamic team environment
- Valid driver’s license (if applicable)

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