Sr. Associate/Manager – Clinical Information Management

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 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.

Eli Lilly Cork is made up of a talented diverse team of over 2,000 employees across 60 nationalities who deliver innovative solutions that add value across a variety of Business Service functions including Finance, Information Technology, Medical, Clinical Trials and more. Eli Lilly Cork offers a premium workspace across our campus in Little Island, complete with flexible hybrid working options, healthcare, pension and life assurance benefits, subsidised canteen, onsite gym, travel subsidies and on-site parking. Inhouse People Development services, Educational Assistance, and our 'Live Your BEST Life' wellbeing initiatives are just some of the holistic benefits that enhance the career experience for our colleagues.

Eli Lilly Cork is committed to diversity, equity and inclusion (DEI). We cater for all dimensions ensuring inclusion of all ethnicities, nationalities, cultural backgrounds, generations, sexuality, visible and invisible disabilities and gender, with four pillars: EnAble, Age & Culture, LGBTQ+ and GIN-Gender Inclusion Network. EnAble, our pillar for people with disabilities and those that care for them, partners with the Access Lilly initiative to make our physical and digital environment accessible and inclusive for all.

Organization Overview: Clinical Trial Foundations (CTF), as part of Clinical Design, Delivery and Analytics (CDDA), delivers innovative and reliable systems, processes, and information to enable clinical development and speed medicines to patients. Clinical information management focuses on establishing and managing a single digitized source of information and assists with enabling use by downstream business units with the aim of ensuring timely, accurate and quality delivery of that information.

The role requires the individual to work across multiple systems, data domains, processes, functions, and locations to ensure accuracy and integrity of the data that supports global drug development.

Responsibilities:

• Maintain and grow a strong working knowledge of the various systems used across CDDA in clinical trials.
• Use expertise in business process understanding, development, and support to manage CDDA business systems.
• Apply knowledge and experience to continuously improve functionality and efficiency of supporting systems.
• Partner across functions, geographies and vendor staff as needed to assist with system integrations and data flows.
• Support internal audits and external inspections as needed.
• Follow standards and procedures for information management ensuring high data quality.
• Provide input into the development of processes and plans for maintaining data quality.
• Ensure processes, data flow, data definitions and other key info related to data sources are documented and maintained.
• Drive shared learning with team members and business partners to ensure consistency and effective management of cross domain data touch points and relationships.
• Collaborate with IT and System SMEs to obtain data needed by consumers, including new data sources.
• Continually seek and implement means of improving processes to reduce cycle time and decrease work effort resulting in cost saving and rapid access to data.
• Understand the confidential nature of company information and take necessary steps to ensure its protection along with understanding various aspects of privacy as it relates to the data.
• Support customer requests for data and ensure accuracy of deliverables.

Basic Requirements:

• Bachelor's degree in Computer Science or IT, preferred.
• Applied experience in medical, quality, clinical drug development, or clinical information flow, preferred.

Additional Skills/Preferences:

• Advanced degree in relevant field.
• Experience in clinical development data systems as well as current and evolving technologies to support clinical development.
• Knowledge and/or experience in project management of data migration and reporting.
• Good interpersonal and leadership skills.
• Excellent oral and written communication skills.
• Demonstrated strength in logical thought, problem solving ability and critical thinking.
• Ability and experience in building consensus and resolving conflict to drive progress.
• Flexibility in approach and/or high learning agility.
• Ability to adjust to unexpected business opportunities while also being a catalyst for positive change.
• Knowledge of regulatory and quality requirements governing clinical data development.
• Exceptional customer focus.
• Strong collaboration and teamwork skills.
• Attention to detail.

Additional Information:

• Limited travel: 0-10%.
• Location: GBS Cork, Cork, Ireland.

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 for further assistance.

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.