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 ... to analysis; 3 years of experience applying knowledge of clinical/drug development and ...
$79K - $91K/yr
Eli Lilly and Company seeks a Clinical Trials Data Associate (P1) to be responsible for trial-level ... to analysis; 3 years of experience applying knowledge of clinical/drug development and ...
$79K - $91K/yr
Eli Lilly and Company seeks a Clinical Trials Data Associate (P1) to be responsible for trial-level ... to analysis; 3 years of experience applying knowledge of clinical/drug development and ...
Create, update, and validate Python-based scripts used for data extraction, transformation, QC ... Clinical Trials Team Partnership * Work closely with the CT Data & Project Lead and CT Data ...
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Create, update, and validate Python-based scripts used for data extraction, transformation, QC ... Clinical Trials Team Partnership * Work closely with the CT Data & Project Lead and CT Data ...
Boston, MA · On-site
... and rigorous analysis of data. The Clinical Trials Specialist will engage in a variety of ... Actual compensation is determined based on several factors, that may include seniority, education ...
Boston, MA · On-site
... and rigorous analysis of data. The Clinical Trials Specialist will engage in a variety of ... Actual compensation is determined based on several factors, that may include seniority, education ...
Determine when to build, buy, partner, or integrate based on user value, vendor maturity ... your Clinical Trials data" experiences across priority datasets. * Use modern AI, analytics ...
Determine when to build, buy, partner, or integrate based on user value, vendor maturity ... your Clinical Trials data" experiences across priority datasets. * Use modern AI, analytics ...
Princeton, NJ · On-site
... clinical trials and data gathered. He/she will ensure that processes and protocols are followed ... Health Advocate and Employee Assistance Program Location Princeton, NJ preferred; applicants based ...
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Princeton, NJ · On-site
... clinical trials and data gathered. He/she will ensure that processes and protocols are followed ... Health Advocate and Employee Assistance Program Location Princeton, NJ preferred; applicants based ...
New York, NY · On-site
Evaluate coverage based on Mondo codes and identify gaps for synonyms and * related concepts ... Prioritize clinical trials and assess opportunities for content expansion (e.g., biomarkers, prior ...
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New York, NY · On-site
Evaluate coverage based on Mondo codes and identify gaps for synonyms and * related concepts ... Prioritize clinical trials and assess opportunities for content expansion (e.g., biomarkers, prior ...
Brooklyn, NY · On-site
$20 - $30/hr
Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but ... home options available.
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Brooklyn, NY · On-site
$20 - $30/hr
Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but ... home options available.
... analysis and submissions of clinical trial data. Position Summary: The Clinical Programming ... Expert level of knowledge in CDISC based e-submission (creation of ADaM datasets and associated ...
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... analysis and submissions of clinical trial data. Position Summary: The Clinical Programming ... Expert level of knowledge in CDISC based e-submission (creation of ADaM datasets and associated ...
Washington, DC · On-site
Protocol Data Analyst I Department: Research Employment Type: Full Time Location: National Institue ... This role codes clinical trials using the NCI Thesaurus, abstracts biomarkers, processes accrual ...
Washington, DC · On-site
Protocol Data Analyst I Department: Research Employment Type: Full Time Location: National Institue ... This role codes clinical trials using the NCI Thesaurus, abstracts biomarkers, processes accrual ...
$155K - $175K/yr
At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO ... This is a home-based role, offering flexibility while providing the opportunity to lead global and ...
$155K - $175K/yr
At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO ... This is a home-based role, offering flexibility while providing the opportunity to lead global and ...
... data collection and storage, biostatistics, and regulation guiding the conduct of research with ... based applications. May produce complex documents, perform analysis and maintain databases.
... data collection and storage, biostatistics, and regulation guiding the conduct of research with ... based applications. May produce complex documents, perform analysis and maintain databases.
Brooklyn, NY · On-site +1
$20 - $30/hr
Clinical Trials Recruiter Location ... Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but ...
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Brooklyn, NY · On-site +1
$20 - $30/hr
Clinical Trials Recruiter Location ... Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but ...
NC · On-site +1
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... Strong analytical and problem solving skills. * Independent and autonomous project oversight skills.
NC · On-site +1
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... Strong analytical and problem solving skills. * Independent and autonomous project oversight skills.
The Project Manager, Clinical Trials, serves as the primary client-facing leader for a portfolio of ... Monitor DICOM data receipt, analysis, reconciliation, and escalation workflows within VIDA and with ...
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The Project Manager, Clinical Trials, serves as the primary client-facing leader for a portfolio of ... Monitor DICOM data receipt, analysis, reconciliation, and escalation workflows within VIDA and with ...
Anaheim, CA · On-site
$29 - $34/hr
Organizes research information for clinical trials. * Observes subjects and assists with data analysis and reporting. * Schedules the collection of data. * Documents adverse events, protocol ...
Anaheim, CA · On-site
$29 - $34/hr
Organizes research information for clinical trials. * Observes subjects and assists with data analysis and reporting. * Schedules the collection of data. * Documents adverse events, protocol ...
Honolulu, HI · On-site
$125K - $130K/yr
Responsible for all protocol data collection including completion of initial study forms, treatment forms and follow-up forms. Enters all patient tracking information into OnCore Clinical Trials ...
Honolulu, HI · On-site
$125K - $130K/yr
Responsible for all protocol data collection including completion of initial study forms, treatment forms and follow-up forms. Enters all patient tracking information into OnCore Clinical Trials ...
The department manager manages staff including clinical trials coordinators, data specialists, finance analysts, regulatory coordinators and research assistants, and any other staff deemed necessary ...
The department manager manages staff including clinical trials coordinators, data specialists, finance analysts, regulatory coordinators and research assistants, and any other staff deemed necessary ...
$34.38 - $38.46/hr
We are looking for a highly motivated and qualified candidate with experience in clinical trials data management. Specific Job Duties: * Coordinates and manages the clinical data for various phases ...
$34.38 - $38.46/hr
We are looking for a highly motivated and qualified candidate with experience in clinical trials data management. Specific Job Duties: * Coordinates and manages the clinical data for various phases ...
Perform in depth analysis of research operation workflows and data collection methods. * Create ... Participate in the integration efforts between the Network Clinical Trials Management System and ...
Perform in depth analysis of research operation workflows and data collection methods. * Create ... Participate in the integration efforts between the Network Clinical Trials Management System and ...
Durham, NC · On-site +1
... Clinical Trials organization globally. * Analyze data and market research to determine trends ... The final salary will be determined based on relevant experience, performance, education, and ...
Durham, NC · On-site +1
... Clinical Trials organization globally. * Analyze data and market research to determine trends ... The final salary will be determined based on relevant experience, performance, education, and ...
$17.31 - $21.28
8% of jobs
$21.28 - $25.26
7% of jobs
$29.24 is the 25th percentile. Wages below this are outliers.
$25.26 - $29.24
9% of jobs
$29.24 - $33.22
19% of jobs
The median wage is $34.71 / hr.
$33.22 - $37.19
17% of jobs
$40.67 is the 75th percentile. Wages above this are outliers.
$37.19 - $41.17
17% of jobs
$41.17 - $45.15
14% of jobs
$45.15 - $49.13
6% of jobs
$49.13 - $53.10
2% of jobs
$53.10 - $57.08
1% of jobs
$57.08 - $61.06
0% of jobs
$17
$36
$61
| Aspect | Home Based Clinical Trials Data Analyst | Clinical Data Coordinator |
|---|---|---|
| Credentials | Bachelor's degree in health, life sciences, or related field; experience with data analysis tools | Bachelor's degree; experience with data entry and database management |
| Work Environment | Remote, flexible hours, analyzing clinical trial data | Typically office-based or site-based, managing data entry and quality control |
| Industry Usage | Used in pharmaceutical, biotech, and research organizations for data analysis | Commonly employed in clinical research sites and CROs for data management |
The Home Based Clinical Trials Data Analyst primarily focuses on analyzing clinical trial data remotely, utilizing statistical tools and software. In contrast, the Clinical Data Coordinator manages data entry, validation, and database maintenance, often working on-site or in a clinical setting. Both roles require knowledge of clinical data processes but differ in their core responsibilities and work environments.
$79K - $91K/yr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 8 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