Clinical Trials Data Associate (P1)
$79K - $91K/yr
Eli Lilly and Company seeks a Clinical Trials Data Associate (P1) to be responsible for trial-level clinical data strategy including database structure, content and meaning, acquisition, storage ...
$79K - $91K/yr
Eli Lilly and Company seeks a Clinical Trials Data Associate (P1) to be responsible for trial-level clinical data strategy including database structure, content and meaning, acquisition, storage ...
$79K - $91K/yr
Eli Lilly and Company seeks a Clinical Trials Data Associate (P1) to be responsible for trial-level clinical data strategy including database structure, content and meaning, acquisition, storage ...
Indianapolis, IN · On-site
$79K - $91K/yr
Eli Lilly and Company seeks a Clinical Trials Data Associate (P1) to be responsible for trial-level clinical data strategy including database structure, content and meaning, acquisition, storage ...
Indianapolis, IN · On-site
$79K - $91K/yr
Eli Lilly and Company seeks a Clinical Trials Data Associate (P1) to be responsible for trial-level clinical data strategy including database structure, content and meaning, acquisition, storage ...
Indianapolis, IN · On-site
We are seeking a Clinical Trials Manager - Patient Engagement to develop and deliver patient recruitment and retention strategies across clinical trial programs. This role combines strategic thinking ...
Indianapolis, IN · On-site
We are seeking a Clinical Trials Manager - Patient Engagement to develop and deliver patient recruitment and retention strategies across clinical trial programs. This role combines strategic thinking ...
$90K - $100K/yr
Clinical Research Site Manager (Lead CRC or Senior CRC with Management Experience) Location: Merrillville, IN Job Type: Full-Time Schedule: Monday-Friday (5x8 shifts) Salary Range: $95K to $110K ...
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$90K - $100K/yr
Clinical Research Site Manager (Lead CRC or Senior CRC with Management Experience) Location: Merrillville, IN Job Type: Full-Time Schedule: Monday-Friday (5x8 shifts) Salary Range: $95K to $110K ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct medical screenings, physical exams, and assessments of study participants. * Provide clinical oversight ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct medical screenings, physical exams, and assessments of study participants. * Provide clinical oversight ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best ...
Indianapolis, IN · On-site
$28 - $37/hr
Support the conduct of oncology clinical trials across Phases I-IV, ensuring adherence to study protocols and timelines. * Assist with patient visits by scheduling, preparing visit documentation, and ...
Indianapolis, IN · On-site
$28 - $37/hr
Support the conduct of oncology clinical trials across Phases I-IV, ensuring adherence to study protocols and timelines. * Assist with patient visits by scheduling, preparing visit documentation, and ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best ...
Maintains effective data management system to track and report patient recruitment for the clinical trials. Assists with administrative activities generally associated with the conduct of the ...
Maintains effective data management system to track and report patient recruitment for the clinical trials. Assists with administrative activities generally associated with the conduct of the ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct medical screenings, physical exams, and assessments of study participants. * Provide clinical oversight ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct medical screenings, physical exams, and assessments of study participants. * Provide clinical oversight ...
We are currently seeking board-certified physicians to serve as Principal or Sub-Investigators in ongoing and upcoming clinical trials. Physicians will oversee participant care, ensure protocol ...
We are currently seeking board-certified physicians to serve as Principal or Sub-Investigators in ongoing and upcoming clinical trials. Physicians will oversee participant care, ensure protocol ...
Indianapolis, IN · On-site
$32 - $43.75/hr
Independently lead the cross-functional study team in the development and execution of complex clinical trials and ensure delivery of clinical milestones on trial(s) with quality, on time, and within ...
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Indianapolis, IN · On-site
$32 - $43.75/hr
Independently lead the cross-functional study team in the development and execution of complex clinical trials and ensure delivery of clinical milestones on trial(s) with quality, on time, and within ...
Indianapolis, IN · On-site
$40 - $45/hr
Clinical Research Nurse - Oncology (Phase I Trials) This clinical research nurse role focuses on supporting phase I oncology clinical trials by providing direct patient care during study visits. The ...
Indianapolis, IN · On-site
$40 - $45/hr
Clinical Research Nurse - Oncology (Phase I Trials) This clinical research nurse role focuses on supporting phase I oncology clinical trials by providing direct patient care during study visits. The ...
We are currently seeking board-certified physicians to serve as Principal or Sub-Investigators in ongoing and upcoming clinical trials. Physicians will oversee participant care, ensure protocol ...
We are currently seeking board-certified physicians to serve as Principal or Sub-Investigators in ongoing and upcoming clinical trials. Physicians will oversee participant care, ensure protocol ...
Indianapolis, IN · Hybrid
$28 - $35/hr
Clinical Research Navigator - Oncology This role supports oncology clinical trials by identifying eligible patients, coordinating their enrollment, and serving as a central liaison between patients ...
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Indianapolis, IN · Hybrid
$28 - $35/hr
Clinical Research Navigator - Oncology This role supports oncology clinical trials by identifying eligible patients, coordinating their enrollment, and serving as a central liaison between patients ...
This position is not eligible for sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to ...
This position is not eligible for sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to ...
Indianapolis, IN · On-site
$217K/yr
The Associate Director, Clinical Development Trial Lead (CDTL) independently leads the cross-functional study team in the development and execution of complex clinical trials and is accountable both ...
Indianapolis, IN · On-site
$217K/yr
The Associate Director, Clinical Development Trial Lead (CDTL) independently leads the cross-functional study team in the development and execution of complex clinical trials and is accountable both ...
Single point of accountability for the Trial Master File for assigned trials, working closely with ... Ensure inspection readiness of respective clinical trial(s). Ensures timely documentation of ...
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Single point of accountability for the Trial Master File for assigned trials, working closely with ... Ensure inspection readiness of respective clinical trial(s). Ensures timely documentation of ...
Support and partner with Clinical Study Leads and cross-functional study teams on global oncology trials * Lead day-to-day study management activities across study startup, conduct, maintenance, and ...
Support and partner with Clinical Study Leads and cross-functional study teams on global oncology trials * Lead day-to-day study management activities across study startup, conduct, maintenance, and ...
This position is not eligible for sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to ...
This position is not eligible for sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to ...
$27.45 - $33.27
4% of jobs
$33.27 - $39.09
6% of jobs
$39.09 - $44.92
7% of jobs
$49.28 is the 25th percentile. Wages below this are outliers.
$44.92 - $50.74
9% of jobs
$50.74 - $56.56
15% of jobs
The median wage is $59.13 / hr.
$56.56 - $62.38
18% of jobs
$66.53 is the 75th percentile. Wages above this are outliers.
$62.38 - $68.21
21% of jobs
$68.21 - $74.03
7% of jobs
$74.03 - $79.85
6% of jobs
$79.85 - $85.67
3% of jobs
$85.67 - $91.50
2% of jobs
$27
$59
$91
To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.
Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.
A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

$79K - $91K/yr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 22 hours ago
8.8
Based on 63 frontline employees who took The Breakroom Quiz
11th of 86 rated pharmaceutical
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Eli Lilly and Company seeks a Clinical Trials Data Associate (P1) to be responsible for trial-level clinical data strategy including database structure, content and meaning, acquisition, storage, retrieval, interchange, delivery, and representation. Collaborate with key study partners to define, implement, and deliver clinical data management packages. Provide trial leadership and ownership for a particular trial, set of trials, or programs. Ensure that data management timeline and results are delivered to scope, cost, and time objectives. Drive data flow design through consultation, review, and approval of vendor work. Define and approve data quality and submission outputs and results. #LI-DNI
Position requires a Bachelor's degree in Statistics, Information Technology, Biochemistry, Epidemiology, or a related field and 3 years of experience with data collection, data flow management, data quality, data technology, dataset delivery, archiving, and data standards. Experience must include a minimum of: 3 years of experience with articulating the flow of data from patient to analysis; 3 years of experience applying knowledge of clinical/drug development and collaborating with study team members; 3 years of experience leading development of creative data solutions to address clinical development challenges; 3 years of experience setting and implementing plans to improve complex clinical data management processes and capabilities; and 3 years of experience with Tableau, PowerBI, Python, SAS, 'R' and Shiny for reporting, metrics and visualization, P-SQL, and T-SQL for DMBS. Telecommuting benefit available. #LI-DNI
Job location: Indianapolis, IN.
To apply, please visit https://jobsearch.lilly.com/ and enter job requisition number R-107940 when prompted. Alternatively, please send your resume, cover letter, and a copy of the ad to: Eli Lilly and Company, Lilly Corporate Center, Drop Code 1093, Indianapolis, IN 46285.
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 (https://careers.lilly.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.
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 (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$79,206.00 - $91,086.90 per yearFull-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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Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.
Pharmaceutical product wholesalers
10,000+ Employees
Indianapolis, IN, US
1876