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Hourly Remote Clinical Informatics Jobs in Indiana

BetterHelp

Psychiatrist - Remote

Indianapolis, IN · Remote

$119 - $242/hr

... hourly equivalent CPT codes. Compensation for CPT codes can vary based on clinician's license and ... Remote *Estimated effective hourly earnings are for licensed Psychiatrists and are illustrative ...

BetterHelp

Psychiatrist - (Remote)

Indianapolis, IN · Remote

$120 - $164/hr

Estimated Effective Hourly Earnings*: Earnings between $120 to $164 per hour is based on a 60 ... Assess, screen, diagnose, and prescribe medication as clinically appropriate. * Coordinate ...

Compass Group

Hybrid Remote/Onsite Dietitian

Evansville, IN · On-site +1

$35 - $40/hr

Hourly Pay: $35 - $40 hr. We go the extra mile for our Dietitians with perks designed to support ... Clinical Nutrition Care: Perform comprehensive nutritional assessments and develop individualized ...

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Hourly Remote Clinical Informatics information

What are the most commonly searched types of Remote Clinical Informatics jobs in Indiana? The most popular types of Remote Clinical Informatics jobs in Indiana are:
What are popular job titles related to Hourly Remote Clinical Informatics jobs in Indiana? For Hourly Remote Clinical Informatics jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Hourly Remote Clinical Informatics jobs in Indiana look for? The top searched job categories for Hourly Remote Clinical Informatics jobs in Indiana are:
What cities in Indiana are hiring for Hourly Remote Clinical Informatics jobs? Cities in Indiana with the most Hourly Remote Clinical Informatics job openings:
Hourly Remote Clinical Informatics jobs near you
Infographic showing various Hourly Remote Clinical Informatics job openings in Indiana as of June 2026, with employment types broken down into 2% As Needed, 39% Full Time, 54% Part Time, and 5% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution.
Clinical Data Manager

Clinical Data Manager

Pharmavise Corporation

Indianapolis, IN • Remote

Contractor

Medical, PTO

Posted 28 days ago

Job description

This is a remote position.

The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock. The CDM ensures that data is accurate, consistent, and meets regulatory and protocol-specific requirements. This role collaborates closely with cross-functional teams, including Clinical Operations, Biostatistics, Medical Writing, and Regulatory Affairs, to support timely and compliant study execution. 
Key Responsibilities: 
Design and review Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems to ensure accurate and complete data capture aligned with the study protocol. 
Develop and maintain data management plans (DMPs), data validation specifications, and CRF completion guidelines. 
Oversee data cleaning activities, including the generation, review, and resolution of data queries in collaboration with clinical sites and study teams. 
Perform ongoing data reviews to identify trends, inconsistencies, or protocol deviations. 
Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). 
Manage database lock activities and contribute to the preparation of clinical study reports (CSRs). 
Serve as the primary point of contact for data management vendors and oversee their deliverables. 
Participate in study team meetings and provide status updates related to data quality and timelines. 
Support audit readiness and participate in regulatory inspections when required. 
Minimum Qualifications: 
Bachelor’s degree in Life Sciences, Computer Science, Health Informatics, or related field. Advanced degree is a plus. 
Minimum of 3–5 years of experience in clinical data management within a pharmaceutical, biotech, or CRO environment. 
Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm, Veeva, REDCap). 
Strong understanding of ICH-GCP, FDA regulations, and CDISC standards. 
Experience with data listings, query management, edit check programming, and coding dictionaries (e.g., MedDRA, WHODrug). 
Excellent organizational, analytical, and problem-solving skills. 
Strong communication and collaboration skills across cross-functional teams. 
Experience working on global, multi-site clinical trials preferred. 
In addition to a dynamic and collaborative work environment, we offer a comprehensive benefits package to support our employees\' well-being. Our benefits include paid holidays, Paid Time Off (PTO) policy, and medical insurance to ensure our team members have the flexibility and coverage they need. We believe in fostering a healthy work-life balance while providing the necessary support for professional and personal growth. 
Be part of our network of Subject Matter Experts.
E-Verify Participation:  
Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. For more information on E-Verify, please contact DHS at 888-897-7781 or through their website at dhs.gov/e-verify. 

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