Req#: REF3411PEmployer Industry: Contract Research Organization
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Chance to work on diverse clinical studies across various therapeutic indications
- Supportive and collaborative work environment
- Opportunity to develop skills and expertise in clinical research
- Flexibility to travel up to 75% as part of the role
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 regarding Adverse Events and protocol deviations
- Perform source data verification and manage study risks at the site level
- Conduct project-specific training of site investigators
What is Required (Qualifications):
- College/University degree in Life Sciences or an equivalent combination of education, training, and experience
- 2+ years of independent on-site monitoring experience
- Experience in all types of monitoring visits, in phases I-III
- Full working proficiency in English
- Valid driver’s license (if applicable)
How to Stand Out (Preferred Qualifications):
- Experience in Oncology highly preferred
- Proficiency in MS Office applications
- Strong communication, collaboration, and problem-solving skills
- Ability to plan, multitask, and work in a dynamic team environment
#ClinicalResearch #Oncology #CareerOpportunity #MonitoringExperience #ContractResearch
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