Employer Industry: Clinical Research and Pharmacovigilance
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Flexible work arrangements with the option to work remotely
- Comprehensive training and support for professional development
- Collaborative and multicultural work environment
- Chance to contribute to innovative healthcare solutions through clinical trials
What to Expect (Job Responsibilities):
- Manage comprehensive trial and site administration, including tracking essential documents and reporting safety updates
- Ensure timely collation and distribution of study tools and clinical documents
- Update clinical trial databases and manage clinical supply & non-clinical supply coordination
- Collaborate with investigators for site evaluation, validation, and regulatory submissions
- Prepare and archive clinical documents, ensuring compliance with regulatory standards
What is Required (Qualifications):
- High School Diploma or equivalent with job training in office management, administration, finance, or healthcare
- Fluent in local languages and business proficient in English with excellent communication skills
- Strong IT skills, particularly in MS Office and clinical IT applications, with advanced MS Excel proficiency
- Good understanding of Global and Country/Regional Clinical Research Guidelines
- Ability to work independently and effectively in a matrix multicultural environment
How to Stand Out (Preferred Qualifications):
- Bachelor’s Degree in a relevant field
- Hands-on knowledge of Good Documentation Practices
- Excellent negotiation skills in finance-related areas
- Proactive attitude towards problem-solving and proposing solutions
- Demonstrated commitment to customer focus both internally and externally
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