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 ...
Clinical Data Coordinator (Clinical Research Technician)
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Assists in the conduct of clinical research studies or trials following established protocols and standard operating procedures (SOP). * Assists with identifying and recruiting subjects for clinical ...
Clinical Data Coordinator (Clinical Research Technician)
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Assists in the conduct of clinical research studies or trials following established protocols and standard operating procedures (SOP). * Assists with identifying and recruiting subjects for clinical ...
Associate Director, Clinical Development Trial Lea
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 ...
Associate Director, Clinical Development Trial Lea
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 ...
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 ...
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 ...
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 ...
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 ...
Quick apply
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 ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide. Required Experience * 2+ ...
Clinical Research Nurse
Indianapolis, IN · On-site
The mission of the Indiana University (IU) Simon Comprehensive Cancer Center (IUSCCC) Clinical Trials Office (CTO) is to support and facilitate the conduct of quality clinical research by IUSCCC ...
Clinical Research Nurse
Indianapolis, IN · On-site
The mission of the Indiana University (IU) Simon Comprehensive Cancer Center (IUSCCC) Clinical Trials Office (CTO) is to support and facilitate the conduct of quality clinical research by IUSCCC ...
Associate Vice President Cardiometabolic Health - Incretin Outcome Trials - Clinical Research P[...]
Indianapolis, IN · On-site
$252 - $369.60/hr
Associate Vice President Cardiometabolic Health -- Incretin Outcome Trials -- Clinical Research Physician job at Eli Lilly and Company. Location: Indianapolis, IN. At Lilly, we unite caring with ...
Associate Vice President Cardiometabolic Health - Incretin Outcome Trials - Clinical Research P[...]
Indianapolis, IN · On-site
$252 - $369.60/hr
Associate Vice President Cardiometabolic Health -- Incretin Outcome Trials -- Clinical Research Physician job at Eli Lilly and Company. Location: Indianapolis, IN. At Lilly, we unite caring with ...
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 ...
Collaborate with clinical research staff in the design, conduct and reporting of local clinical trials (for example, sample size, patient commitment, timelines, grants, and governance review ...
Collaborate with clinical research staff in the design, conduct and reporting of local clinical trials (for example, sample size, patient commitment, timelines, grants, and governance review ...
Collaborate with clinical research staff in the design, conduct and reporting of local clinical trials (for example, sample size, patient commitment, timelines, grants, and governance review ...
Collaborate with clinical research staff in the design, conduct and reporting of local clinical trials (for example, sample size, patient commitment, timelines, grants, and governance review ...
Serve as Sub-Investigator or Principal Investigator in clinical trials. * Conduct medical evaluations of participants and assess eligibility. * Monitor safety, adverse events, and treatment response ...
Serve as Sub-Investigator or Principal Investigator in clinical trials. * Conduct medical evaluations of participants and assess eligibility. * Monitor safety, adverse events, and treatment response ...
Clinical Research Coordinator
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Conduct clinical trials that involve human subjects according to written protocols and departmental standards while adhering to Good Clinical Practice (GCP) Guidelines. * Create and complete valid ...
Clinical Research Coordinator
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Conduct clinical trials that involve human subjects according to written protocols and departmental standards while adhering to Good Clinical Practice (GCP) Guidelines. * Create and complete valid ...
Clinical Research Coordinator
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Conduct clinical trials that involve human subjects according to written protocols and departmental standards while adhering to Good Clinical Practice (GCP) Guidelines. * Create and complete valid ...
Clinical Research Coordinator
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Conduct clinical trials that involve human subjects according to written protocols and departmental standards while adhering to Good Clinical Practice (GCP) Guidelines. * Create and complete valid ...
Rheumatologist (Clinical Trial Physician)
Merrillville, IN · On-site
$268K - $346K/yr
Serve as PI or Sub-I on assigned clinical trials. * Conduct medical evaluations and determine participant eligibility. * Monitor patient safety, adverse events, and treatment outcomes. * Review and ...
Quick apply
Rheumatologist (Clinical Trial Physician)
Merrillville, IN · On-site
$268K - $346K/yr
Serve as PI or Sub-I on assigned clinical trials. * Conduct medical evaluations and determine participant eligibility. * Monitor patient safety, adverse events, and treatment outcomes. * Review and ...
Collaborate and complement clinical research staff in the design and conduct of clinical trials (e.g. sample size, patient commitment, timelines, grants, and governance review interactions)
Collaborate and complement clinical research staff in the design and conduct of clinical trials (e.g. sample size, patient commitment, timelines, grants, and governance review interactions)
Clinical Trials information
See Indiana salary details
$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
How much do clinical trials jobs pay per hour?
What are the key skills and qualifications needed to thrive in a clinical trials position, and why are they important?
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.
What are some common career paths or advancement opportunities for professionals working in clinical trials?
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.
What is a clinical trial?
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.
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- Clinical Trials Contracts Manager
- Junior Clinical Research Associate
- Volunteer Icon Clinical Research
- Freelance Clinical Research Associate
- Decentralized Clinical Trials Manager
- Fulltime H1B Clinical Research
- Remote Clinical Research Phlebotomist
- Clinical Research Organization
- Research Studies

$100 - $150/hr
Other
Medical
Re-posted 21 days ago
Job description
Clinical Trial Physician (Multiple Specialties) - Merrillville, IN
Job Type: Part time (8 hours/week)
Shift: Flexible
Job Summary:
A leading clinical research facility is conducting innovative studies across multiple therapeutic areas. 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 compliance, and collaborate with research teams to deliver high-quality trial outcomes.
Specialties:
We are looking for board-certified physicians in the following areas:
Dermatology
Gastroenterology (GI)
Endocrinology
Rheumatology
Psychiatry
Surgery (General & Specialty)
Internal Medicine (Internist: $100-$150/hr)
Note: Cardiology is not being considered at this time.
Roles and Responsibilities:
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Serve as Principal Investigator or Sub-Investigator in clinical trials
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Conduct medical assessments and evaluate participant eligibility
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Monitor patient safety, adverse events, and study outcomes
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Review and sign study-related documentation
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Collaborate with research coordinators and staff
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Maintain compliance with Good Clinical Practice (GCP) guidelines
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Qualifications, Requirements, and Licensure:
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MD or DO degree with an active state medical license
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Board certification in one of the listed specialties
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Interest in clinical research (prior experience is a plus)
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Strong communication and organizational skills
Benefits:
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Competitive compensation: Internists $100-$150/hr; other specialties at market-standard rates
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Flexible scheduling (0 to 8 hours per week)
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Research training and professional development opportunities
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Play a vital role in advancing medical science
About Protouch Staffing
Sourced by ZipRecruiter
Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Frisco, TX, US
Year founded
1989