Clinical Trial Registry Writer
Purpose:
The purpose of the Clinical Trial Registry (CTR) Writer is to support the development and implementation
of Clinical Trial Registry (CTR) systems and processes, ensuring Global transparency regulations and
requirements are described and implemented and that there are monitoring systems (and metrics) in place to ensure compliance.
The CTR writer will collaborate with cross-functional, multidisciplinary teams across multiple geographies and
phases of drug development to ensure/coordinate the accurate and timely posting of applicable clinical trial protocol information and study results.
Minimum Qualification Requirements:
• Bachelor's degree in scientific, health, communications, or technology related field
• Or, Bachelor's degree in any field with at least two years of clinical development
• Demonstrated high-level end-user computer skills (MS office applications: Word, Excel, PowerPoint, ).
• Demonstrated mastery of English language skills written and spoken. Other Information/Additional Preferences:
• Experience with CTR processes
• Experience in biostatistics, medical/regulatory
• Verbal reasoning, attention to detail, critical thinking, and analytical
• Demonstrated project management and time management
• Ability to be flexible in varying environments and with multiple customer
• Able to work independently as well as part of a team: able to take initiative and responsibility, following through and completing assigned tasks.
• Able to deal with ambiguity and to plan, prioritize, and manage conflicting
• Experience working within multiple functional areas across medical, regulatory and
• Strong interpersonal and negotiation skills - Ability to manage
• Strong medical research background with demonstrated breadth and depth of knowledge of medical research processes throughout all phases of development.
• Developed networks and proven ability to influence cross-functionally at all
• Ability to influence/lead
• Ability to work well across cultures and time
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