... clinical studies. Responsibilities: The job tasks listed below outline the scope of the position ... Collaborate with team members to write reports and communicate results. * Assist with, or be ...
... clinical studies. Responsibilities: The job tasks listed below outline the scope of the position ... Collaborate with team members to write reports and communicate results. * Assist with, or be ...
... that will assist our clients in developing and marketing life-changing therapies to positively ... Substantial clinical study protocol experience, as lead author, required * Experience leading and ...
Quick apply
... that will assist our clients in developing and marketing life-changing therapies to positively ... Substantial clinical study protocol experience, as lead author, required * Experience leading and ...
Clinical Research Nurse
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 ...
New
Quick apply
Clinical Research Nurse
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 ...
New
Participate in development of safety-related data collection forms for clinical studies ... Develop or update strategy and content for regional risk management plans * Assist GSOs to oversee ...
Participate in development of safety-related data collection forms for clinical studies ... Develop or update strategy and content for regional risk management plans * Assist GSOs to oversee ...
Clinical Research Coordinator
$23 - $30.50/hr
... Assist project manager(s) with study start-up Attend and participate in team meetings Collect ... clinical research and independently coordinate the activities of 1 or more large-scale, complex ...
Clinical Research Coordinator
$23 - $30.50/hr
... Assist project manager(s) with study start-up Attend and participate in team meetings Collect ... clinical research and independently coordinate the activities of 1 or more large-scale, complex ...
Clinical Research Coordinator
Clermont, IN · On-site
$23 - $30.50/hr
... Assist project manager(s) with study start-up Attend and participate in team meetings Collect ... clinical research and independently coordinate the activities of 1 or more large-scale, complex ...
Clinical Research Coordinator
Clermont, IN · On-site
$23 - $30.50/hr
... Assist project manager(s) with study start-up Attend and participate in team meetings Collect ... clinical research and independently coordinate the activities of 1 or more large-scale, complex ...
... study design, data interpretation, and dissemination of findings relevant to clinical and ... Center * Assist in identifying training needs in evidence-based prevention and therapy for ...
... study design, data interpretation, and dissemination of findings relevant to clinical and ... Center * Assist in identifying training needs in evidence-based prevention and therapy for ...
... study design, data interpretation, and dissemination of findings relevant to clinical and ... Center * Assist in identifying training needs in evidence-based prevention and therapy for ...
... study design, data interpretation, and dissemination of findings relevant to clinical and ... Center * Assist in identifying training needs in evidence-based prevention and therapy for ...
Clinical Research Specialist
Indianapolis, IN · On-site
$43K - $47K/yr
Job Summary The Clinical Research Specialist will assist with enrollment of participants into a ... Conducts study visit activities and coordinates screening, consenting, and scheduling of test ...
Clinical Research Specialist
Indianapolis, IN · On-site
$43K - $47K/yr
Job Summary The Clinical Research Specialist will assist with enrollment of participants into a ... Conducts study visit activities and coordinates screening, consenting, and scheduling of test ...
Position Summary Under the direction of department leadership, Assistant, Clinical Research is ... research studies including processing specimens, entering data, maintaining files, etc.
Position Summary Under the direction of department leadership, Assistant, Clinical Research is ... research studies including processing specimens, entering data, maintaining files, etc.
Position SummaryUnder the direction of department leadership, Assistant, Clinical Research is ... research studies including processing specimens, entering data, maintaining files, etc.
Position SummaryUnder the direction of department leadership, Assistant, Clinical Research is ... research studies including processing specimens, entering data, maintaining files, etc.
Under the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including processing ...
Under the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including processing ...
Clinical Research Coordinator II - New Albany, IN
$22.50 - $29.75/hr
Manage a full schedule of complex study visits and corresponding tasks with minimal direction ... Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related ...
Clinical Research Coordinator II - New Albany, IN
$22.50 - $29.75/hr
Manage a full schedule of complex study visits and corresponding tasks with minimal direction ... Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related ...
Clinical Research Coordinator II - New Albany, IN
New Albany, IN · On-site
$22.50 - $29.75/hr
Manage a full schedule of complex study visits and corresponding tasks with minimal direction ... Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related ...
Clinical Research Coordinator II - New Albany, IN
New Albany, IN · On-site
$22.50 - $29.75/hr
Manage a full schedule of complex study visits and corresponding tasks with minimal direction ... Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related ...
Clinical Research Coordinator II - New Albany, IN
$22.50 - $29.75/hr
Manage a full schedule of complex study visits and corresponding tasks with minimal direction ... Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related ...
Quick apply
Clinical Research Coordinator II - New Albany, IN
$22.50 - $29.75/hr
Manage a full schedule of complex study visits and corresponding tasks with minimal direction ... Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related ...
Clinical Research Coordinator I -RN
$63K - $80K/yr
Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times. * Assist with routine data verification and quality control, ensuring data integrity and ...
Clinical Research Coordinator I -RN
$63K - $80K/yr
Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times. * Assist with routine data verification and quality control, ensuring data integrity and ...
The Clinical Research Physician must be aware of, and ensure that all activities of the medical ... * Assist in planning process and participate in study start-up meetings and other activities to ...
The Clinical Research Physician must be aware of, and ensure that all activities of the medical ... * Assist in planning process and participate in study start-up meetings and other activities to ...
Clinical Research Coordinator I -RN
New Albany, IN · On-site
$63K - $80K/yr
Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times. * Assist with routine data verification and quality control, ensuring data integrity and ...
Clinical Research Coordinator I -RN
New Albany, IN · On-site
$63K - $80K/yr
Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times. * Assist with routine data verification and quality control, ensuring data integrity and ...
Clinical Research Coordinator I -RN
$63K - $80K/yr
Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times. * Assist with routine data verification and quality control, ensuring data integrity and ...
Quick apply
Clinical Research Coordinator I -RN
$63K - $80K/yr
Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times. * Assist with routine data verification and quality control, ensuring data integrity and ...
The Clinical Research Physician must be aware of, and ensure that all activities of the medical ... * Assist in planning process and participate in study start-up meetings and other activities to ...
The Clinical Research Physician must be aware of, and ensure that all activities of the medical ... * Assist in planning process and participate in study start-up meetings and other activities to ...
Clinical Study Assistant information
See Indiana salary details
$10.98 - $12.48
1% of jobs
$12.48 - $13.97
5% of jobs
$13.97 - $15.47
15% of jobs
$15.77 is the 25th percentile. Wages below this are outliers.
$15.47 - $16.97
20% of jobs
The median wage is $17.95 / hr.
$16.97 - $18.47
14% of jobs
$18.47 - $19.96
13% of jobs
$19.96 - $21.46
7% of jobs
$21.51 is the 75th percentile. Wages above this are outliers.
$21.46 - $22.96
8% of jobs
$22.96 - $24.45
9% of jobs
$24.45 - $25.95
4% of jobs
$25.95 - $27.45
3% of jobs
$10
$19
$27
How much do clinical study assistant jobs pay per hour?
What are the main challenges a Clinical Study Assistant might face when supporting clinical trial operations?
What is the difference between Clinical Study Assistant vs Clinical Research Coordinator?
| Aspect | Clinical Study Assistant | Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in health sciences or related field | Usually requires a bachelor's degree, often with additional certifications in clinical research |
| Work Environment | Supports clinical trials in hospitals, research centers, or pharmaceutical companies | Manages entire clinical studies, coordinating between sites, staff, and sponsors |
| Employer & Industry | Hospitals, research institutions, pharmaceutical companies | Academic medical centers, hospitals, research organizations |
| Search & Comparison Intent | Often compared for entry-level roles supporting clinical trials | Compared for roles with broader responsibilities in clinical study management |
The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.
What do clinical trial assistants do?
Is CRA an entry level job?
What are Clinical Study Assistants?
What qualifications do I need to be a clinical research assistant?
Is CRA better than CRC?
What are the key skills and qualifications needed to thrive as a Clinical Study Assistant, and why are they important?

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 14 days ago
Eli Lilly and Company rating
8.8
Based on 63 frontline employees who took The Breakroom Quiz
8th of 74 rated pharmaceutical
Job description
Overview:
Our Global Statistical Sciences department includes over 200 people with advanced degrees in Statistics/Biostatistics. Our diverse population of global talent brings innovation to every aspect of our business - from Discovery Research to Clinical Development to Manufacturing and Real-world Evidence. We are playing a leading role in transforming the way the company develops medicines using state-of-the-art methods in adaptive designs, Bayesian statistics, causal inference, genetic/biomarker analysis, machine learning and more!
The Clinical Project Statistician (Advisor - Statistics) develops or assists in the development of protocol designs, clinical plans, and data analysis plans in collaboration with physicians, clinical research scientists, and/or medical colleagues. The Clinical Project Statistician is responsible for working with research associates and scientists to establish a reporting database, determining the appropriate statistical analysis procedures, and for analyzing data in clinical studies.
Responsibilities:
The job tasks listed below outline the scope of the position. The application of these tasks may vary, based upon current business needs.
Statistical Trial Design and Analysis
- Operate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study.
- Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol and the statistical analysis plan, and conducting the actual analysis once a reporting database is created.
- Collaborate with data sciences in the planning and implementation of data quality assurance plans.
- Keep up to date with novel statistical methodology, maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected.
- Influence team members regarding appropriate research methods
- Perform peer-review of work products from other statistical colleagues.
Communication of Results and Inferences
- Collaborate with team members to write reports and communicate results.
- Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings.
- Respond to regulatory queries and interact with regulators.
Therapeutic Area Knowledge
- Understand disease states, competitive landscapes, and regulatory environment in order to enhance the level of customer focus and collaboration and be seen as a key scientific contributor.
Regulatory Compliance
- Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes, and training.
Statistical leadership and Teamwork
- Introduce and apply innovative methodology and tools to solve critical problems
- Merge scientific thinking and business knowledge to identify issues, evaluate options and implement solutions.
- Lead projects independently and work effectively across functions. Apply technical expertise to influence business decisions.
Requirements:
- Ph.D. degree in Statistics OR Biostatistics and expected graduation before August 2027
Desired Experience:
- Proficient in statistical programming languages/software such as SAS, R, Python, etc
- Interpersonal communication skills for effective customer consultation
- Teamwork and leadership skills
- Technical expertise and application with working knowledge of experimental design and statistical analysis
- Self-management skills with a focus on results for timely and accurate completion of competing deliverables
- Resource management skills
- Creativity and innovation
- Demonstrated problem solving ability and critical thinking
- Business process expertise associated with critical activities (e.g. regulatory submissions)
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
$151,500 - $222,200
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.
#WeAreLilly
What Eli Lilly and Company employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Eli Lilly
Sourced by ZipRecruiter
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.
Industry
Pharmaceutical product wholesalers
Company size
10,000+ Employees
Headquarters location
Indianapolis, IN, US
Year founded
1876