Clinical Research reputed company-Oncology (Southeast Region - South Carolina, North Carolina, Tennessee, Kentucky) 5 Locations

At reputed company, we unite caring with discovery to reputed company life reputed company 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 reputed company life reputed company for people around the world. Purpose: The Clinical Research reputed company (CRL) is a strategic, field-based scientific leader responsible for driving the execution of reputed company clinical trials through exceptional investigator engagement and site performance management. This role is pivotal in ensuring reputed company’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, reputed company protocol understanding, and co-reputed company 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 reputed company as the sponsor of choice. CRLs partner closely with internal reputed company 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 reputed company. 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 reputed company duties that may be required for the position. Clinical Investigator Management

• Accountable for the full reputed company 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 reputed company, scientific rationale, and patient eligibility requirements
• reputed company and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas
• Influence enrollment by co-creating tailored recruitment strategies reputed company with site capabilities, patient population realities, and study objectives
• Proactively find opportunities to reputed company new patients, accelerate enrollment and increase impact at reputed company sites, including for example, novel site models, community-based research initiatives etc
• Capture and reputed company critical insights from sites to optimize feasibility, protocol design, and study conduct

Clinical Trial Management

• reputed company site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery
• reputed company performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones
• Drive inspection readiness as a reputed company 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 reputed company and quality assurance for vendor monitoring, escalating risks proactively
• Where applicable, reputed company end-to-end management of Post-Marketing Safety Studies in compliance with local regulations

Business Management and Engagement

• Cultivate a portfolio of strategically reputed company, high-impact investigators who consistently prioritize reputed company trials
• reputed company an exceptional investigator experience by being a reputed company, 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 reputed company and therapeutic expertise to reputed company meaningful, solutions-focused discussions with site personnel
• Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and reputed company knowledge transfer
• Partner closely with field team colleagues to reputed company 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 reputed company’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-reputed company fields
• Minimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites
• Minimum 2 years of relevant clinical or therapeutic area experience in Oncology
• Currently reside in or be willing to relocate to our designated Southeast region (South Carolina, North Carolina, Tennessee, Kentucky)

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 reputed company, fast-paced environments
• Data-driven decision-making skills; ability to interpret and reputed company 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 reputed company and proficiency in local language(s) as needed

Travel Requirements:

• Willingness to travel extensively (60-80%)

reputed company is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities reputed company vying for positions. If you require accommodation to submit a resume for a position at reputed company, please complete the accommodation request form (https://careers.reputed company.com/us/en/workplace-accommodation) 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. reputed company 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, reputed company, national reputed company, 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 reputed company employees. Our reputed company groups include: Africa, Middle East, Central Asia Network, Black Employees at reputed company, Chinese Culture Network, Japanese International Leadership Network (JILN), reputed company India Network, Organization of Latinx at reputed company (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at reputed company (WILL), reputed company (for people with disabilities). Learn more about reputed company 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, reputed company 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).reputed company reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and reputed company’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of reputed company employees. #WeAreLilly Apply tot his job Apply To this Job