Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines. * Review source documents and medical records to ensure complete and accurate ...
Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines. * Review source documents and medical records to ensure complete and accurate ...
Clinical Operations Associate (Pool)
CA · Remote
$70K - $80K/yr
Medical
Retirement
PTO
Our mission is to bring innovation to clinical trial execution through passion, transparency, co ... This is an exciting entry-level opportunity to join a fast-paced and dynamic learning environment ...
Clinical Operations Associate (Pool)
CA · Remote
$70K - $80K/yr
Medical
Retirement
PTO
Our mission is to bring innovation to clinical trial execution through passion, transparency, co ... This is an exciting entry-level opportunity to join a fast-paced and dynamic learning environment ...
Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines. * Review source documents and medical records to ensure complete and accurate ...
Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines. * Review source documents and medical records to ensure complete and accurate ...
Clinical Trial Associate
Newark, CA · On-site
$86K - $105K/yr
Medical
Dental
Vision
Life
Retirement
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Perform data verification and reconciliation of study trackers against EDC, CTMS, and other ...
Clinical Trial Associate
Newark, CA · On-site
$86K - $105K/yr
Medical
Dental
Vision
Life
Retirement
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Perform data verification and reconciliation of study trackers against EDC, CTMS, and other ...
Clinical Trial Associate
Manhattan, NY · On-site
$36.75 - $50.25/hr
Support ongoing maintenance of the Clinical Trial Management System (CTMS), ensuring data accuracy and timeliness * Review, file, and track clinical trial documentation in accordance with SOPs and ...
Clinical Trial Associate
Manhattan, NY · On-site
$36.75 - $50.25/hr
Support ongoing maintenance of the Clinical Trial Management System (CTMS), ensuring data accuracy and timeliness * Review, file, and track clinical trial documentation in accordance with SOPs and ...
Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines. * Review source documents and medical records to ensure complete and accurate ...
Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines. * Review source documents and medical records to ensure complete and accurate ...
Clinical Research & Data Coordinator
Atlanta, GA · On-site
$23.25 - $31/hr
Manage clinical trial data sets, ensuring accuracy, consistency, and security. Ensure that all clinical trial data are accurately entered into electronic data capture (EDC) systems and promptly ...
Clinical Research & Data Coordinator
Atlanta, GA · On-site
$23.25 - $31/hr
Manage clinical trial data sets, ensuring accuracy, consistency, and security. Ensure that all clinical trial data are accurately entered into electronic data capture (EDC) systems and promptly ...
Clinical Trial Psych Rater - Hungarian Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
New
Clinical Trial Psych Rater - Hungarian Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
New
Clinical Trial Psych Rater - Hungarian Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
New
Clinical Trial Psych Rater - Hungarian Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
New
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater - Hungarian Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
New
Clinical Trial Psych Rater - Hungarian Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
New
Clinical Trial Psych Rater
Colton, CA · Remote
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater
Colton, CA · Remote
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater - Hungarian Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
New
Clinical Trial Psych Rater - Hungarian Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
New
Clinical Trial Associate/Clinical Research Coordinator
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. Primary Responsibilities:
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Clinical Trial Associate/Clinical Research Coordinator
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. Primary Responsibilities:
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater
Boston, MA · Remote
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater
Boston, MA · Remote
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater
Mesa, AZ · Remote
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater
Mesa, AZ · Remote
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Manager
Boston, MA · On-site
$100K - $125K/yr
Work closely with Data Management to ensure ongoing data cleaning including review of data ... Global Phase 3 clinical trial management experience * Minimum of 3 years of clinical trial ...
Clinical Trial Manager
Boston, MA · On-site
$100K - $125K/yr
Work closely with Data Management to ensure ongoing data cleaning including review of data ... Global Phase 3 clinical trial management experience * Minimum of 3 years of clinical trial ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Review case data and prepare for rater discussions, ensuring all relevant documents and scale items ...
Entry Level Clinical Trial Data Transparency information
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$13.94 - $20.56
5% of jobs
$20.56 - $27.19
6% of jobs
$29.74 is the 25th percentile. Wages below this are outliers.
$27.19 - $33.81
35% of jobs
The median wage is $34.45 / hr.
$33.81 - $40.43
38% of jobs
$40.43 - $47.05
6% of jobs
$47.05 - $53.67
3% of jobs
$53.67 - $60.29
2% of jobs
$60.29 - $66.91
0% of jobs
$66.91 - $73.54
0% of jobs
$73.54 - $80.16
1% of jobs
$80.16 - $86.78
3% of jobs
$13
$38
$86
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Full-time
Posted 11 days ago
Job description
The Clinical Research Data Entry Specialist is responsible for accurately entering, reviewing, and maintaining clinical trial data in EDC systems. This role supports clinical research studies by ensuring data quality, completeness, and compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. This position is ideal for a detail-oriented individual with data entry or administrative experience who is interested in building a career in clinical research.
ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. Using our proprietary technology, we aim to:
- Increase patient access to research trials within our communities
- Provide physicians with enhanced care options for current patients
- Deliver superior clinical research enrollment metrics to Pharma sponsors
All with the ultimate goal of Improving Patient Outcomes at the Point of Care . We want you to join us in doing just that.
Key Responsibilities:
- Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines.
- Review source documents and medical records to ensure complete and accurate transcription of participant data.
- Verify data for accuracy, completeness, and consistency prior to submission.
- Review, investigate, and resolve EDC data queries generated by sponsors, contract research organizations (CROs), or data management teams by comparing source documentation and collaborating with study personnel.
- Communicate with Clinical Research Coordinators, investigators, and other study staff to resolve missing, incomplete, or inconsistent data.
- Correct data discrepancies while maintaining appropriate documentation and audit trails within the EDC system.
- Ensure timely completion of data entry and query resolution to support study milestones and database lock.
- Maintain accurate study documentation related to data entry activities.
- Adhere to study protocols, sponsor requirements, Good Clinical Practice (GCP), HIPAA, and applicable regulatory guidelines.
- Assist with quality control reviews and support sponsor monitoring visits, audits, and regulatory inspections as needed.
- Maintain confidentiality of participant information and research data.
Qualifications:
- High school diploma or equivalent.
- 1+ years of data entry, administrative support, medical office, or related experience.
- Excellent attention to detail and data accuracy.
- Strong organizational and time management skills.
- Ability to manage multiple priorities and meet deadlines in a fast-paced environment.
- Strong written and verbal communication skills.
Requirements
This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant
About ObjectiveHealth
Sourced by ZipRecruiter
Company size
51 - 200 Employees
Headquarters location
Franklin, TN, US
Year founded
2018