Lilly Assoc. Manager- Clinical Trial Registry in Bengaluru, India
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 35,000 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.
Clinical Trial Registry Writer
Associate Level - Position title and level may vary by site location.
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.
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( LillyRecruitingCompliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. 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.
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!