Real Worl Evidence

4 weeks ago

Riyadh, Saudi Arabia Lilly Full time

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 demand for high quality health economic and outcomes research (HEOR) and real-world evidence (RWE) to support drug development, health technology assessment/access decisions, product differentiation, and clinical decision making continues to increase. The purpose of the Lilly Value, Evidence, and Outcomes (VEO) team is to accelerate equitable patient access and transform healthcare delivery through the execution and communication of bold, high impact science. We are looking for talented, energetic, creative, diverse, influential, and collaborative team members to join the VEO function and Team Lilly.

**Path/Level**:
P3

**Responsibilities**:
Provides technical and project administrative support to selected hubs or affiliates to help enable on-time and on-budget delivery of key tasks during RWE project execution.
- Facilitates delivery of project milestones with quality on time, on budget, and within scope.
- Ensures that cost, timelines, scope and risk management processes are in place to monitor and control performance of the overall project that utilizes appropriate tools and techniques.
- Hold supportive functions accountable for achievement of key project deliverables in alignment with the agreed project plan and in compliance with corporate quality standards.
- Facilitates Vendor Requests for Proposals (RFPs), contracting, internal documentation and archiving, Risk, Privacy and Quality assessments, PO set-up, invoice processing, record management in Pangaea.
- Takes on research management tasks tracking the progress of the studies across key milestones and presenting regular updates on the status of all studies to the RWE affiliate Heads.
- Ensures good documentation practices. Uploads study protocols, reports and other study documents in the appropriate system for review, approval and storage.
- Works with functions to align resources based upon team prioritization decisions.
- Facilitates discussions with TPOs to manage team priorities.
- Contribute to RWE process improvements.

**Facilitates and supports knowledge management of RWE activity in KSA**
- Provides leadership and expertise on how to utilize Pangaea and other relevant tools to ensure effective knowledge and management of data sources, RWE studies and projects in the IBU region.
- Ensures the information contained in Pangaea is updated and accurate. Conduct quality checks to ensure the accuracy and completeness of the information contained in our data sources.
- Runs regular reports to provide updates to internal stakeholders on key metrics such as volume of RWE activity, type and cost of projects and how the RWE deliverables are used internally.
- Influences decision-making by translating results into actionable options/scenarios.

**Project Management**
- Accountable for delivering the prioritized RWE research on time and on budget, ensuring study/ project budgets are realistic.
- Effectively communicates status of RWE projects to key business partners to keep them informed of project status, budget implications, etc.,

**Professional Development**:

- Keep up to date on trainings for professional development.
- Ensure my PM objectives are completed in line with company process.
- Understanding and adherence to all company policies and procedures

**Basic Requirements**:

- Bachelor’s Degree preferably in a scientific or health-related field:

- At least 2-3 years’ experience in clinical research and/or knowledge in health outcomes research.

**Knowledge and Experience**:

- Knowledge, experience and understanding of the use of healthcare data used in outcomes research.
- Demonstrated knowledge and experience with project management tools and process.
- Experience in medical, scientific or technical writing fields (at least 1 year)
- Strong comprehension and communication skills including the ability to translate and disseminate complex scientific information in a clear and concise manner.
- Knowledge and experience of local health care systems
- Understanding of and experience with clinical research and market access environment.

**Skills**:

- Demonstrable strong communication and interpersonal skills and the ability to work successfully in a cross-functional environment.
- Fluency in local language and English
- Demonstrated ability to influence individuals.
- Demonstrated project management skills.

**Other role requirements**:

- Saudi Nationals only
- T

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