Employer Industry: Clinical Research Organization

Why Consider this Job Opportunity:
- Competitive total reward package with an excellent level of base pay
- Wide range of variable pay and recognition programs
- Best in class employee benefits and supportive policies
- Opportunities for career development and growth within the organization
- Home-based position in the United States
- Comprehensive training and continuous learning culture

What to Expect (Job Responsibilities):
- Manage all documents and logistical tasks related to clinical trials
- Ensure compliance with GCP, SOPs, and local regulatory requirements
- Track progress of clinical trials and manage study data, budget, and investigational products
- Maintain trial, country, and site level protocol information in trial management systems
- Prepare study files for investigational sites and coordinate development of associated documents

What is Required (Qualifications):
- BA/BS degree in Life Sciences, Nursing, or related field
- 1-2 years of relevant clinical trial experience
- Proficient in English language (spoken and written)
- Strong knowledge of MS Office applications
- Strong interpersonal and negotiating skills

How to Stand Out (Preferred Qualifications):
- Experience in VeevaVault TMF is desirable

#ClinicalResearch #ClinicalTrials #CareerDevelopment #RemoteWork #CompetitiveCompensation

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