The Overnight Study Monitor’s primary purpose is to assist with study operation in the absence of the clinical coordinators. They will ensure overnight study activities occur as scheduled and all associated documents are complete.
- Conduct activities at scheduled times.
- Accurately report study data on source documents.
- Communicate with other staff to provide organized completion of activities.
- Execute other duties as assigned.
Required: High School Diploma or Equivalent.
Knowledge, Skills, Abilities: Communication, teamwork, ability to give directions to a group of people.
Skills Required
- High School Diploma or Equivalent
- Effective communication skills
- Teamwork
- Ability to give directions to a group
What We Do
AXIS Clinicals Limited is one of the most experienced and fastest growing Clinical Research Organization. Our state-of-the-art facilities houses 500+ dedicated full-time professionals to ensure the quick turn around time with high quality. Our facilities are accredited by DCGI (Drugs Controller General – India), NABL (National Accreditation Board for Testing and Calibration Laboratories - ISO 15189:2003) and inspected by US-FDA, UK-MHRA, Brazil-ANVISA, France –AFSSAPS / ANSM, GCC, MCC-South Africa etc. Within short span, we have achieved the milestone of completing 2750+ clinical studies and 1000+ product approvals from various regulatory agencies. 65+ regulatory audits from global competent authorities is testament to our professionalism and dedication to quality studies. Our Phase II – IV capabilities are growing along with an extended portfolio of Site Management, Medical Writing, and Data Management.
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