Clinical Research Coordinator
$22.25 - $29.50/hr
We emphasize standardization and centralization of clinical trial operations to ensure efficiency, high-quality data, and faster study start-up timelines. With a patient-centric approach and ...
Clinical Research Coordinator
$22.25 - $29.50/hr
We emphasize standardization and centralization of clinical trial operations to ensure efficiency, high-quality data, and faster study start-up timelines. With a patient-centric approach and ...
Clinical Research Associate *This role is located in either Ohio or Michigan The Clinical Research ... In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance.
Clinical Research Associate *This role is located in either Ohio or Michigan The Clinical Research ... In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance.
Clinical Research Associate *This role is located in either Ohio or Michigan The Clinical Research ... In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance.
Clinical Research Associate *This role is located in either Ohio or Michigan The Clinical Research ... In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance.
Clinical Research Associate *This role is located in either Ohio or Michigan The Clinical Research ... In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance.
Clinical Research Associate *This role is located in either Ohio or Michigan The Clinical Research ... In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance.
Clinical Research Associate *This role is located in either Ohio or Michigan The Clinical Research ... In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance.
Clinical Research Associate *This role is located in either Ohio or Michigan The Clinical Research ... In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance.
... study start up, maintenance, close out, and database lock, depending on the client's needs. In this client dedicated role, you will work on-site to provide administrative and technical support by ...
... study start up, maintenance, close out, and database lock, depending on the client's needs. In this client dedicated role, you will work on-site to provide administrative and technical support by ...
... study start up, maintenance, close out, and database lock, depending on the client's needs. In this client dedicated role, you will work on-site to provide administrative and technical support by ...
... study start up, maintenance, close out, and database lock, depending on the client's needs. In this client dedicated role, you will work on-site to provide administrative and technical support by ...
... study start up, maintenance, close out, and database lock, depending on the client's needs. In this client dedicated role, you will work on-site to provide administrative and technical support by ...
... study start up, maintenance, close out, and database lock, depending on the client's needs. In this client dedicated role, you will work on-site to provide administrative and technical support by ...
... study start up, maintenance, close out, and database lock, depending on the client's needs. In this client dedicated role, you will work on-site to provide administrative and technical support by ...
... study start up, maintenance, close out, and database lock, depending on the client's needs. In this client dedicated role, you will work on-site to provide administrative and technical support by ...
Clinical Research Coordinator
$23 - $30.50/hr
... study start-up Attend and participate in team meetings Collect, process and ship laboratory specimens Schedule subject visits and procedures in EMR and keep track of visits Complete subject visits ...
Clinical Research Coordinator
$23 - $30.50/hr
... study start-up Attend and participate in team meetings Collect, process and ship laboratory specimens Schedule subject visits and procedures in EMR and keep track of visits Complete subject visits ...
Clinical Research Coordinator
$23 - $30.50/hr
... study start-up Attend and participate in team meetings Collect, process and ship laboratory specimens Schedule subject visits and procedures in EMR and keep track of visits Complete subject visits ...
Clinical Research Coordinator
$23 - $30.50/hr
... study start-up Attend and participate in team meetings Collect, process and ship laboratory specimens Schedule subject visits and procedures in EMR and keep track of visits Complete subject visits ...
Warehouse Sr. Industrial Engineer - Start-ups (remote)
Indianapolis, IN · On-site +1
$75K - $100K/yr
Previous start-up experience required (including pre start-up and/or post start-up experience ... Applies engineering methodologies/tools such as product slotting, studying labor standards (time ...
Warehouse Sr. Industrial Engineer - Start-ups (remote)
Indianapolis, IN · On-site +1
$75K - $100K/yr
Previous start-up experience required (including pre start-up and/or post start-up experience ... Applies engineering methodologies/tools such as product slotting, studying labor standards (time ...
... study start-up meetings and other activities to provide the appropriate training and information to ... Support medical information associates in preparation and review of medical letters and other ...
... study start-up meetings and other activities to provide the appropriate training and information to ... Support medical information associates in preparation and review of medical letters and other ...
Research Operations Lead
Warsaw, IN · On-site
... study start-up and activation activities, including protocol finalization support, data use agreement execution, and site/vendor readiness - Manage research compliance documentation across all HEMA ...
Research Operations Lead
Warsaw, IN · On-site
... study start-up and activation activities, including protocol finalization support, data use agreement execution, and site/vendor readiness - Manage research compliance documentation across all HEMA ...
... study start-up and activation activities, including protocol finalization support, data use agreement execution, and site/vendor readiness - Manage research compliance documentation across all HEMA ...
... study start-up and activation activities, including protocol finalization support, data use agreement execution, and site/vendor readiness - Manage research compliance documentation across all HEMA ...
Injection Molding Set-up Tech
Lafayette, IN · On-site
$17/hr
Associates are eligible for benefits such as medical/dental, 401(k), and PTO. Applicants with ... Apply now to start your new career! Available Shifts: * 2nd Shift: 2:00pm-10:30pm (potential daily ...
Injection Molding Set-up Tech
Lafayette, IN · On-site
$17/hr
Associates are eligible for benefits such as medical/dental, 401(k), and PTO. Applicants with ... Apply now to start your new career! Available Shifts: * 2nd Shift: 2:00pm-10:30pm (potential daily ...
Evenings Operations Pharmacist - Investigational Drug Services
Indianapolis, IN · On-site
$55.75 - $67/hr
Support study start-up and maintenance activities as needed * Collaborate with IDS pharmacists, study coordinators, and research teams to resolve protocol-related questions * Maintain audit-ready ...
Evenings Operations Pharmacist - Investigational Drug Services
Indianapolis, IN · On-site
$55.75 - $67/hr
Support study start-up and maintenance activities as needed * Collaborate with IDS pharmacists, study coordinators, and research teams to resolve protocol-related questions * Maintain audit-ready ...
Support study start-up and maintenance activities as needed * Collaborate with IDS pharmacists, study coordinators, and research teams to resolve protocol-related questions * Maintain audit-ready ...
Support study start-up and maintenance activities as needed * Collaborate with IDS pharmacists, study coordinators, and research teams to resolve protocol-related questions * Maintain audit-ready ...
Cx Associate Project Managers are responsiblefor generating business, providing general management ... Experience leading commissioning/start-up activities for construction projects exceeding $25MM in ...
Cx Associate Project Managers are responsiblefor generating business, providing general management ... Experience leading commissioning/start-up activities for construction projects exceeding $25MM in ...
Cx Associate Project Managers are responsiblefor generating business, providing general management ... Experience leading commissioning/start-up activities for construction projects exceeding $25MM in ...
Cx Associate Project Managers are responsiblefor generating business, providing general management ... Experience leading commissioning/start-up activities for construction projects exceeding $25MM in ...
Study Start Up Associate information
See Indiana salary details
$12.12 - $15.80
3% of jobs
$15.80 - $19.48
18% of jobs
$20.21 is the 25th percentile. Wages below this are outliers.
$19.48 - $23.16
20% of jobs
The median wage is $25.40 / hr.
$23.16 - $26.85
15% of jobs
$26.85 - $30.53
11% of jobs
$30.53 - $34.21
4% of jobs
$37.34 is the 75th percentile. Wages above this are outliers.
$34.21 - $37.89
5% of jobs
$37.89 - $41.57
8% of jobs
$41.57 - $45.25
6% of jobs
$45.25 - $48.93
6% of jobs
$48.93 - $52.61
3% of jobs
$12
$30
$52
How much do study start up associate jobs pay per hour?
As of Jun 20, 2026, the average hourly pay for study start up associate in Indiana is $30.01, according to ZipRecruiter salary data. Most workers in this role earn between $20.14 and $39.57 per hour, depending on experience, location, and employer.
What is the difference between Study Start Up Associate vs Clinical Trial Coordinator?
| Aspect | Study Start Up Associate | Clinical Trial Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, knowledge of regulatory requirements | Bachelor's degree, familiarity with clinical procedures |
| Work Environment | Regulatory and site initiation activities | Participant management and site coordination |
| Employer & Industry Usage | Pharmaceuticals, biotech, CROs | Hospitals, research centers, CROs |
The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.
What are popular job titles related to Study Start Up Associate jobs in Indiana? For Study Start Up Associate jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Study Start Up Associate jobs in Indiana look for? The top searched job categories for Study Start Up Associate jobs in Indiana are:
What cities in Indiana are hiring for Study Start Up Associate jobs? Cities in Indiana with the most Study Start Up Associate job openings:
$22.25 - $29.50/hr
Other
Posted 11 days ago
Job description
P1 Pratia Oncology (formerly P1 Trials) is a network of world-class, community-based oncology investigative sites capable of performing complex Phase 1 clinical trials. We emphasize standardization and centralization of clinical trial operations to ensure efficiency, high-quality data, and faster study start-up timelines. With a patient-centric approach and collaboration with our pharmaceutical, biotech, and CRO partners, we are dedicated to delivering reliable outcomes that support groundbreaking medical advancements. As our team continues to grow in the US, we are hiring a clinical research coordinator who will support the safe, compliant, and efficient conduct of early-phase oncology clinical trials across the P1 Pratia Network.
As a Clinical Research Coordinator, you will:
- Assist with daily clinical trial activities from study start-up through close-out.
- Schedule and facilitate study visits, assessments, and follow-up appointments.
- Support investigational product accountability when delegated.
- Track and document protocol deviations; support corrective actions.
- Assist with site qualification, initiation, monitoring, and close-out visits.
- Conduct pre-screening and confirm eligibility according to protocol criteria.
- Coordinate labs, imaging, procedures, and specialist referrals.
- Document protocol compliance, including investigational product adherence.
- Maintain essential regulatory documents per ICH-GCP, FDA, and institutional standards.
- Support IRB submissions, amendments, safety reports, and renewals.
- Maintain delegation logs and protocol version control.
- Promote adherence to SOPs and process improvement initiatives.
- Enter and verify data in EDC systems within sponsor timelines.
- Resolve data queries promptly and collaborate with monitors.
- Oversee completion of case report forms (CRFs).
- Assist with audits and inspections.
- Coordinate with Pharmacy for IP accountability and dispensing when delegated.
- Coordinate with Laboratory for specimen processing and shipping.
- Coordinate with Radiology for protocol-window imaging.
- Document and follow up on adverse events (AEs) and serious adverse events (SAEs).
- Report safety events per protocol and regulatory timelines.
- Assist with feasibility, qualification, and study start-up activities.
- Track study visit completion and billable items.
Knowledge, Skills and Abilities
- Working knowledge of ICH-GCP and FDA regulations
- Attention to detail and accuracy in documentation, data entry, and regulatory records.
- Proficiency with clinical trial systems (e.g., EDC, CTMS) and standard office software.
Requirements
- High school diploma or GED
- Prior experience as a CRC or equivalent clinical research role (oncology preferred).
The anticipated salary range for this role is 65-80k/yearly. Actual compensation will depend on experience, location, and other factors.
Candidates must be authorized to work in the United States without current or future sponsorship.