Clinical Research Lead - (Cardiometabolic Health, Investigator Engagement (Southeast)

JOB 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.

Purpose :

The Clinical Research Lead (CRL) is a strategic, field-based scientific leader responsible for driving the execution of Lilly clinical trials through exceptional investigator engagement and site performance management. This role is pivotal in ensuring Lilly’s portfolio is prioritized at high-performing sites and that trials are delivered with quality, speed, and insight.

CRLs combine deep therapeutic and scientific knowledge with strategic agility to influence investigators, elevate protocol understanding, and co-develop tailored enrollment strategies in existing and new therapeutic areas. They serve as trusted partners to investigators—building strong, enduring relationships that improve return on enrollment and position Lilly as the sponsor of choice. CRLs partner closely with internal Lilly teams (including Clinical Development and Medical Affairs) to ensure that insights from the field shape development strategies and that development strategies are delivered with operational excellence and scientific clarity.

Where applicable the CRL may also represent Investigator Engagement with Regulatory and External Bodies and help shape the country-level clinical trial landscape.

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.

Clinical Investigator Management

Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout

Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements

Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas

Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives

Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc

Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct

Clinical Trial Management

Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery

Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones

Drive inspection readiness as a continuous discipline across sites

Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality

Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country / site selection and protocol localization

Provide oversight and quality assurance for vendor monitoring, escalating risks proactively

Where applicable, lead end-to-end management of Post-Marketing Safety Studies in compliance with local regulations

Business Management and Engagement

Cultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize Lilly trials

Enable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner

Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity

Conduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution

Maintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel

Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer

Partner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships

Country / Regulatory Engagement (where applicable)

Represent Investigator Engagement with regulatory agencies, ethics committees, and national research organizations in countries / territory

Influence the clinical trial ecosystem to improve regulatory agility and operational feasibility

Ensure that local requirements are translated into compliant, efficient trial execution and that Lilly’s internal processes reflect evolving country landscapes

Partner with leadership to identify and align regional initiatives and contribute to enterprise-wide clinical development success

Minimum Qualification Requirements :

Bachelor’s degree or equivalent; strong preference for scientific, clinical, or health-related fields

Minimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites

Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position

Candidate must currently reside in or be willing to relocate to the Southeast region of the United States

Other Information / Additional Preferences :

Advanced degree in a scientific or clinical field (PharmD, PhD, MD, or MSc preferred)

Excellent understanding of GCP, clinical development and operations, and trial lifecycle

Demonstrated understanding of the therapeutic landscape and standards of care, with the ability to apply this knowledge to decision making

Proven ability to build credibility and influence HCP community through scientific acumen and relationship strength

Strategic approach with demonstrated success in delivering results in complex, fast-paced environments

Data-driven decision-making skills; ability to interpret and act on performance and operational metrics

Excellent communication, negotiation, and organizational skills

Deep therapeutic area knowledge and familiarity with local clinical research ecosystems

Experience directly influencing clinical site performance and driving enrollment success

Track record of delivering or exceeding performance targets in a collaborative matrix environment

Experience working with regulators or national bodies in support of clinical trial delivery

English fluency and proficiency in local language(s) as needed

Travel Requirements :

Willingness to travel extensively (60-80%)

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. 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 is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include : Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$111,000 - $195,800

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and / or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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