Job title: Assoc. Manager- Clinical Trial Registry
Company: Eli Lilly
Job description: Clinical Trial Registry Writer Associate Level – Position title and level may vary by site location. Purpose: The purpose of the Clinical Trial Registry (CTR) Writer is to support the development and implementation of Clinical Trial Registry (CTR) sy
Clinical Trial Registry Writer Associate Level – Position title and level may vary by site location. 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 experience. . Demonstrated high-level end-user computer skills (MS office applications: Word, Excel, PowerPoint, etc.). . Demonstrated mastery of English language skills written and spoken. Other Information/Additional Preferences: . Experience with CTR processes and databases. . Experience in biostatistics, medical/regulatory writing. . Verbal reasoning, attention to detail, critical thinking, and analytical ability. . Demonstrated project management and time management skills. . Ability to be flexible in varying environments and with multiple customer groups. . 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 priorities. . Experience working within multiple functional areas across medical, regulatory and legal. . Strong interpersonal and negotiation skills – Ability to manage upwards. . 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 levels. . Ability to influence/lead others. . Ability to work well across cultures and time zones. . Willingness to travel as required.
Expected salary:
Location: Bangalore, Karnataka
Job date: Thu, 16 Jun 2022 22:31:43 GMT
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