Employer Industry: Clinical Research Organization

Why Consider this Job Opportunity:
- Competitive salary and additional benefits
- Opportunities for career advancement and growth within the organization
- Inclusive work environment fostering innovation and excellence
- Diverse culture rewarding high performance and nurturing talent
- Well-being and work-life balance opportunities for employees and their families

What to Expect (Job Responsibilities):
- Organize Study Team meetings and prepare meeting minutes
- Assist with organizing Investigator Meetings
- Assist with site management activities and enrollment tracking
- Submit study documentation to Trial Master File
- Contribute to department initiatives and process improvement efforts

What is Required (Qualifications):
- Bachelor's degree in life sciences discipline or relevant field preferred
- 2 years of relevant work experience in the biopharmaceutical industry
- Basic knowledge of GCP, CFR, and ICH guidelines
- Ability to work well with cross-functional Study Team and investigational sites
- Proficiency in Microsoft Office applications

How to Stand Out (Preferred Qualifications):
- Experience in clinical trial operations
- Strong attention to detail and ability to work under pressure with tight timelines

#ClinicalResearch #CareerOpportunity #CompetitivePay #Innovation #InclusiveCulture

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