Associate -Clinical Trial Registry Writing at Lilly

Bengaluru, karnataka, India -

Full Time

Start Date

Immediate

Expiry Date

06 Jan, 26

Salary

0.0

Posted On

08 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Registry, Document Management, Project Management, Biostatistics, Medical Writing, Regulatory Writing, Attention to Detail, Critical Thinking, Analytical Ability, Interpersonal Skills, Negotiation Skills, Flexibility, Teamwork, Time Management, Medical Research, Cross-Functional Collaboration

Industry

Pharmaceutical Manufacturing

Description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Organization Overview: The purpose of the Associate, GSC Clinical Trial Registry Writing 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. Responsibilities: Clinical Trial Registry and Results Planning, Development, Finalization and Document Management ▪ Contribute to the development, maintenance, and implementation of policies and/or procedures on clinical trial registry and clinical trial results database processes and work flows. Identify opportunities for process improvements. ▪ Identify studies required for registry and results postings. Ensure that responsible functions are aware of timelines and deadlines. ▪ Collaborate cross functionally with applicable team members and departments (e.g.,biostats, medical, clinical trial management), to obtain data required for completion of registry and results entries. ▪ Manage access rights to applicable systems as needed. ▪ Serves as subject matter expert on CTR database requirements. ▪ Develop and provide education and training as required to internal groups. ▪ Define and monitor applicable metrics to support overall compliance. ▪ Maintains and enhances knowledge of CTR regulations and guidelines. ▪ Exhibits flexibility in moving across therapeutic areas and compounds, depending on project assignment, etc. Project Management / Influence / Knowledge Sharing ▪ Supports the systems and process for CTR and works with other team members to ensure consistent practices are monitored and employed globally. ▪ Provides input to deliver innovative solutions, preventing re-occurrence of issues. ▪ Escalates issues in a timely and appropriate manner. ▪ Ensures the evaluation (monitoring) of the CTR processes and communicating changes to the processes to the business. ▪ Shares key learning to drive simplification and replicate best practices. Basic 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. Additional Skills/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. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. #WeAreLilly At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe! #WeAreLilly

Responsibilities

The Associate will support the development and implementation of Clinical Trial Registry systems and processes, ensuring compliance with global transparency regulations. They will collaborate with cross-functional teams to ensure the accurate and timely posting of clinical trial information and results.