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Temporary Clinical Trial Data Entry Jobs (NOW HIRING)

System One

Data Coordinator

Brentwood, TN · On-site

Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...

System One

Data Coordinator

Brentwood, TN · On-site

Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...

System One

Data Coordinator

Brentwood, TN · On-site

Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...

System One

Data Coordinator

Brentwood, TN · On-site

Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...

System One

Data Coordinator

Brentwood, TN · On-site

Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Perform primary review of submitted clinical data, database entry, and source document verification ...

System One

Data Coordinator

Brentwood, TN · On-site

Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Perform primary review of submitted clinical data, database entry, and source document verification ...

Consumer Product Testing Company, Inc.

Be Seen First

Clinical Trial Technician

Fairfield, NJ · On-site

$20 - $22/hr

The Clinical Trial Technician position is based within our Clinical Patch Testing department and ... and data entry into Excel platform. · Peer review trial data as required for accuracy, data ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Support CTMS and other clinical system activities, including data entry, quality and validation ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Support CTMS and other clinical system activities, including data entry, quality and validation ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Support CTMS and other clinical system activities, including data entry, quality and validation ...

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Temporary Clinical Trial Data Entry information

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How much do temporary clinical trial data entry jobs pay per hour?

As of Aug 9, 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?

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 is a temporary clinical trial data entry?

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?

AspectTemporary Clinical Trial Data EntryClinical Data Coordinator
CredentialsHigh school diploma or equivalent; data entry experienceBachelor's degree in life sciences or related field; experience in data management
Work EnvironmentTemporary assignments in clinical research settings, often part-time or contractFull-time role in clinical research teams, overseeing data quality
Employer & Industry UsagePharmaceutical companies, CROs, research institutionsPharmaceutical 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:
Temporary Clinical Trial Data Entry jobs near you
Infographic showing various Temporary Clinical Trial Data Entry job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.

Data Coordinator

System One

Brentwood, TN • On-site

Contractor

Re-posted 23 days ago

Job description

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 meet study data needs and deadlines • Data abstraction from diverse sources • Obtain source documentation for patients enrolled into clinical trials and data registry • Maintain Data Registry as directed • Supports Clinical Project Manager to meet industry trial data deadlines • Obtain source documentation for patients enrolled into clinical trial • Assist in SAE reporting and tracking • Create and maintain patient visit tracking spreadsheets • Maintain and archive study documents • Attend meetings as assigned and report on actions • All other duties as assigned Requirements: • High School Diploma Required • Bachelor’s Degree Preferred • 1+ years of experience in healthcare, research, or other science related field • Knowledge of scientific, medical, and regulatory terms • Must have an understanding of clinical research process • Knowledge of GCP and GMP • Computer skills with ability to use clinical trial databases, electronic data capture, MS Access or Excel Ref: #568-Clinical