Clinical Research Data Entry Specialist (Onsite) The Clinical Research Data Entry Specialist is responsible for accurately entering, reviewing, and maintaining clinical trial data in EDC systems.
Clinical Research Data Entry Specialist (Onsite) The Clinical Research Data Entry Specialist is responsible for accurately entering, reviewing, and maintaining clinical trial data in EDC systems.
Description Clinical Research Data Entry Specialist (Onsite) The Clinical Research Data Entry Specialist is responsible for accurately entering, reviewing, and maintaining clinical trial data in EDC
Description Clinical Research Data Entry Specialist (Onsite) The Clinical Research Data Entry Specialist is responsible for accurately entering, reviewing, and maintaining clinical trial data in EDC
Clinical Data Manager
Burlington, MA · Hybrid
What You'll Do: We are seeking a highly skilled and motivated Clinical Data Manager to join our Clinical Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will
Clinical Data Manager
Burlington, MA · Hybrid
What You'll Do: We are seeking a highly skilled and motivated Clinical Data Manager to join our Clinical Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will
Data Entry Clerk
$21 - $26/hr
Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS,
Data Entry Clerk
$21 - $26/hr
Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS,
Data Entry Clerk
$24 - $29/hr
Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS,
Data Entry Clerk
$24 - $29/hr
Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS,
Clinical Data Manager
Burlington, MA · On-site
$145K - $160K/yr
Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics,
Clinical Data Manager
Burlington, MA · On-site
$145K - $160K/yr
Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics,
What You Will Do * Coordinate and facilitate the clinical trial data for participants enrolled in clinical research studies conducted by principal investigator(s) at University Hospitals Case Medical
What You Will Do * Coordinate and facilitate the clinical trial data for participants enrolled in clinical research studies conducted by principal investigator(s) at University Hospitals Case Medical
Company Description Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients'
Company Description Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients'
Company Description Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients'
Company Description Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients'
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison between the recruitment and clinical trials teams to ensure that potential trial subjects are
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison between the recruitment and clinical trials teams to ensure that potential trial subjects are
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison between the recruitment and clinical trials teams to ensure that potential trial subjects are
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison between the recruitment and clinical trials teams to ensure that potential trial subjects are
Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis,
Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis,
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Quick apply
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Quick apply
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis,
Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis,
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Quick apply
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Quick apply
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Quick apply
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Quick apply
Data Coordinator
Brentwood, TN · On-site
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: * Support data entry activities to
Temporary Clinical Trial Data Entry information
See salary details
$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
How much do temporary clinical trial data entry jobs pay per hour?
As of Aug 2, 2026, the average hourly pay for temporary clinical trial data entry in the United States is $38.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $38.94 per hour, depending on experience, location, and employer.
What are some common challenges faced in a Temporary Clinical Trial Data Entry role, and how can they be managed?
One of the main challenges in a Temporary Clinical Trial Data Entry position is maintaining high accuracy and attention to detail while working with large volumes of sensitive data under tight deadlines. It's important to stay organized and follow established protocols to minimize errors and ensure compliance with regulatory standards. Collaborating closely with clinical research coordinators and data managers can help clarify uncertainties and maintain data integrity. Regular communication and seeking feedback from the team are also valuable in overcoming these challenges.
What are the key skills and qualifications needed to thrive as a Temporary Clinical Trial Data Entry specialist, and why are they important?
To thrive as a Temporary Clinical Trial Data Entry specialist, you need strong attention to detail, organizational skills, and familiarity with data management, typically supported by a high school diploma or higher. Proficiency in electronic data capture (EDC) systems, Microsoft Excel, and sometimes Good Clinical Practice (GCP) certification is valuable. Excellent time management, accuracy under pressure, and effective communication are standout soft skills for this position. These skills ensure the integrity, reliability, and timely processing of clinical trial data, which are critical for successful research outcomes.
What are Temporary Clinical Trial Data Entry jobs?
Temporary Clinical Trial Data Entry jobs involve entering, updating, and managing data collected during clinical trials on a short-term or contract basis. These professionals ensure that clinical data is accurately recorded in databases, following strict protocols to maintain data integrity and confidentiality. Tasks may include verifying patient information, inputting test results, and assisting with data audits. Temporary roles are often available during particularly busy phases of a clinical study or to cover for permanent staff absences.
What is the difference between Temporary Clinical Trial Data Entry vs Clinical Data Coordinator?
| Aspect | Temporary Clinical Trial Data Entry | Clinical Data Coordinator |
|---|---|---|
| Credentials | High school diploma or equivalent; data entry experience | Bachelor's degree in life sciences or related field; experience in data management |
| Work Environment | Temporary assignments in clinical research settings, often part-time or contract | Full-time role in clinical research teams, overseeing data quality |
| Employer & Industry Usage | Pharmaceutical companies, CROs, research institutions | Pharmaceutical companies, CROs, biotech firms |
Temporary Clinical Trial Data Entry focuses on inputting data accurately during clinical trials, often on short-term contracts. Clinical Data Coordinators have broader responsibilities, including data validation, management, and ensuring compliance. While both roles require attention to detail, the coordinator role typically demands more experience and a higher level of responsibility.
More about Temporary Clinical Trial Data Entry jobs
What cities are hiring for Temporary Clinical Trial Data Entry jobs? Cities with the most Temporary Clinical Trial Data Entry job openings:
What are the most commonly searched types of Clinical Trial Data Entry jobs? The most popular types of Clinical Trial Data Entry jobs are:
What states have the most Temporary Clinical Trial Data Entry jobs? States with the most job openings for Temporary Clinical Trial Data Entry jobs include:
What job categories do people searching Temporary Clinical Trial Data Entry jobs look for? The top searched job categories for Temporary Clinical Trial Data Entry jobs are:
Full-time
Posted 10 days ago
Job description
Clinical Research Data Entry Specialist (Onsite)
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:
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:
Qualifications:
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
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