Associate Director - Clinical Central Services and Innovation

Associate Director - Clinical Central Services and Innovation page is loaded

Associate Director - Clinical Central Services and Innovation

Apply locations Ireland, Cork time type Full time posted on Posted 7 Days Ago job requisition id R-64435 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. Purpose The Clinical Central Services and Innovation (CCSI) organization orchestrates solutions that strategically enhances clinical research awareness and accessibility while increasing diversity, reducing burden, and speeding trial execution. This group partners across functions within Clinical Design, Delivery and Analytics (CDDA) and Product Research and Development (PRD) to influence trial design and operationalize innovation solutions to support the execution of clinical trials globally for all business units across all phases of development. The Associate Director (P4), Clinical Central Services, and Innovation (CCSI) ensures operational excellence in the design and delivery of clinical capabilities including but not limited to mobile health care, clinical emerging technology & digital solutions, telemedicine, virtual trial orchestration, new site models, central services and/or digital device management. This role is responsible for coordination of third-party relationship management in support of these capabilities. Primary Responsibilities This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position. Services and Capability Expertise

• Understand business strategies, processes, technology, and device management as it relates to clinical services and capabilities.
• Serve as domain expert to ensure data, process and/or technology capabilities are optimized across the CDDA.
• Maintain strategic alignment for clinical services across functional and therapeutic areas.
• Develop and implement strategies to expand and/or evolve capabilities to accelerate and/or increase accessibility within clinical research.
• Continuously maintain a state of inspection readiness. Participate and perform duties required for internal and external inspections as well as supporting institutions/investigators and alternative site locations in inspection readiness initiatives.

Project Management

• Drive adoption, improvement, shared learning, and process expertise across global business partners.
• Develop critical success factors for pilots/projects and monitor progress to ensure clear criteria exists to enable decision making.
• Identify, monitor, and communicate global customer (internal and external) needs/requirements related to process and/or technology performance and improvements.

• Lead organizational change, communication planning and training initiatives.
• Provide guidance and consulting into forecasting and expense management.
• Identify project implementation risks and raise issues appropriately.
• Facilitates issue management.
• Lead progress reporting activities and metrics.

Partnership

• Foster inclusion, innovation, and promote diversity.
• Partner closely within teams to effectively plan, forecast, and manage the portfolio and project work.
• Collaborate with key stakeholders (i.e. , Quality, Privacy, Legal, Tech@Lilly, Procurement, Clinical Trial Foundations) in support of the portfolio .
• Manage relationships with third party organizations (TPOs), contribute to oversight of TPO performance and establishment of associated metrics across the portfolio.
• partner with TPOs to improve customer experience and monitor performance.
• Provide coaching within the organization that fosters inclusion and innovation, continual improvement, and an external awareness and understanding.

Minimum Qualification Requirements

• Bachelor’s degree and 5 years of experience in project management, clinical drug development or a health care related field.
• Knowledge of emerging health care related services and capabilities for clinical research.
• Knowledge of country regulatory guidelines/requirements for clinical research conduct.
• Demonstrated ability to implement strategies to improve processes and capabilities.

Other Information/Additional Preferences

• Strong networking, interpersonal and relationship skills with demonstrated ability to work in teams, across organizational boundaries and achieve results through others.
• Flexibility to adjust quickly to changing business priorities.
• Good interpersonal and leadership skills
• Excellent oral and written communication skills
• Strong business insight.

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 ( Lilly_Recruiting_Compliance@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. #WeAreLilly

Similar Jobs (8)

Associate Director - Clinical Trial Patient Engagement

locations Ireland, Cork time type Full time posted on Posted 30+ Days Ago

Associate Director - Trial Capabilities - Therapeutic Project Lead

locations Ireland, Cork time type Full time posted on Posted 5 Days Ago

Associate Director - Clinical Development Trial Lead (CDTL) - Diabetes and Obesity

locations Ireland, Cork time type Full time posted on Posted Today #J-18808-Ljbffr