Job summary
Job post source
This job is directly from Eli Lilly and Company
Job overview
The Clinical Research Scientist at Eli Lilly leads early-phase clinical trials in diabetes and obesity, impacting drug development and patient care.
Responsibilities and impact
The role involves designing and overseeing Phase I and II clinical trials, collaborating with cross-functional teams, ensuring regulatory compliance, monitoring patient safety, disseminating scientific data, supporting regulatory activities, and providing business and scientific expertise.
Compensation and benefits
The salary range is $168,000 to $294,800 with eligibility for bonuses, 401(k), pension, medical, dental, vision benefits, flexible spending accounts, life insurance, leave benefits, and wellness programs.
Experience and skills
Requires an advanced degree in health/science with 3-5 years clinical or pharmaceutical experience, or a BS/MS with 7-10 years relevant pharmaceutical experience; strong leadership, communication, and teamwork skills are preferred.
Career development
Opportunities include professional development goals, coaching others, participation in committees, and leadership roles in cross-functional teams.
Work environment and culture
Eli Lilly emphasizes diversity, inclusion, employee resource groups, and a supportive environment with a focus on patient advocacy and ethical research.
Company information
Eli Lilly is a global healthcare leader focused on discovering and delivering medicines to improve patient lives worldwide, headquartered in Indianapolis, Indiana.
Team overview
The candidate will join the Diabetes, Obesity & Complications Program team working on early-phase compounds with collaboration across clinical, research, regulatory, and business units.
Unique job features
The role offers involvement in innovative clinical research, global trial execution, regulatory support, and opportunities to engage with external experts and scientific communities.
Company overview
Eli Lilly and Company is a global pharmaceutical firm specializing in the development and commercialization of innovative medicines. They generate revenue primarily through the sale of prescription drugs across various therapeutic areas, including oncology, immunology, neuroscience, and diabetes. Founded in 1876, Eli Lilly has a rich history of pioneering medical advancements, such as the mass production of insulin and the development of the polio vaccine. The company is headquartered in Indianapolis, Indiana, and continues to invest heavily in research and development to bring new treatments to market.
How to land this job
Position your resume to emphasize your advanced degree in health, medical, or scientific fields and highlight 3-5 years of clinical or pharmaceutical experience, especially in clinical development and trial execution.
Focus on showcasing your expertise in designing and overseeing Phase I and II clinical trials, protocol development, and collaboration with multidisciplinary teams including pharmacokinetics, statistics, and regulatory affairs.
Apply through multiple channels such as Eli Lilly’s corporate careers page, LinkedIn, and other job boards where the position is posted to maximize your application’s reach.
Connect with current employees in the Diabetes, Obesity & Complications division on LinkedIn; use ice breakers like commenting on recent Lilly clinical trial innovations or asking about their experience working on early-phase compounds targeting diabetes and weight management.
Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical trial design,' 'pharmacokinetics,' 'GCP compliance,' 'regulatory support,' and 'data dissemination' to ensure it passes initial screenings.
Leverage Jennie Johnson’s Power Apply feature to automate tailored resume submissions, find the best job portals, and identify LinkedIn contacts for networking, allowing you to focus more on interview preparation and skill enhancement.
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