
Clinical Trials Coordinator Specialist
6 days ago
Job Description
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- We simplify and modernize clinical trials for thousands of investigators and research site staff.">
- This role drives faster, safer, and more efficient clinical trials, leading to improved quality of life and lives saved.">
Key Responsibilities
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- Develop training materials and tools for Clinical Research Specialists (CRS) Level 1.">
- Assist with updating clinical operations process guides.">
- Conduct quality checks on previous projects as part of risk assessment.">
- Review client documents to determine project timelines.">
- Help plan and backlog projects as delegated.">
- Analyze complex scientific/medical/pharmaceutical information.">
- Collaborate with study teams and internal project teams for timely delivery.">
- Design and structure clinical information for efficient product use.">
- Monitor and analyze user feedback and usage metrics.">
Additional Responsibilities
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- Assist with translation tasks across departments and perform study demos in local languages.">
Benefits
">Faster, safer, and more efficient clinical trials for a better quality of life and lives saved.
">Requirements
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- Expertise in developing training materials and tools.">
- Ability to analyze complex scientific/medical/pharmaceutical information.">
- Strong collaboration skills with study teams and internal project teams.">
- Experience in monitoring and analyzing user feedback and usage metrics.">
Skills and Qualifications
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- Advanced degree in a related field or equivalent experience.">
- Excellent communication and interpersonal skills.">
- Proven analytical and problem-solving skills.">
- Ability to work in a fast-paced environment with multiple priorities.">
What We Offer
">A challenging and rewarding career opportunity in the clinical trials industry.
">A collaborative and dynamic work environment.
">Ongoing training and professional development opportunities.
"]",-
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