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Temporary Clinical Trial Data Entry Jobs (NOW HIRING)

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

... clinical trial data management activities from study start-up to database lock. * Develop and implement data management plans, data validation plans, edit check plans and data entry guidelines in ...

NeevSys Inc

Clinical Trials SME

Rockville, MD

Patient and Clinician Trial Search Support - Define and validate data requirements that enable accurate patient- and clinician-facing clinical trial search, including disease terms, biomarkers ...

Micro Typing Systems

Clinical Trials Associate

Athens, OH

$26.50 - $36.25/hr

Assists with data entry as necessary, and audits field clinical trial data for inclusion in regulatory submissions. Help implement and maintain clinical trial tracking databases for each clinical ...

QuidelOrtho

Clinical Trials Associate

Athens, OH · On-site

$26.50 - $36.25/hr

Assists with data entry as necessary, and audits field clinical trial data for inclusion in regulatory submissions. Help implement and maintain clinical trial tracking databases for each clinical ...

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

As of May 28, 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 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 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 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?

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 May 2026, with employment types broken down into 2% Locum Tenens, 4% Internship, 81% Full Time, 2% Part Time, 2% Temporary, and 9% Contract. Highlights an 71% Physical, and 29% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.

Clinical Data Manager

MapLight Therapeutics

Burlington, MA • Hybrid

Other

Posted 9 days ago

Job description

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 play a pivotal role in ensuring the integrity, accuracy, and completeness of clinical trial data, contributing to the successful development and regulatory approval of our products.

 Responsibilities:

  • Manage and lead all aspects of clinical trial data management activities from study start-up to database lock.
  • Develop and implement data management plans, data validation plans, edit check plans and data entry guidelines in compliance with regulatory standards and company SOPs.
  • Collaborate with cross-functional teams including Clinical Operations, Biostatistics, and Regulatory Affairs to ensure data quality and integrity throughout the trial lifecycle.
  • Oversee Medidata Rave electronic data capture (EDC) system setup, configuration, user management, coding and data extracts.
  • Perform data cleaning, discrepancy management, SAE and vendor integration reconciliation activities to ensure timely database lock.
  • Conduct periodic data reviews and generate weekly data quality metrics to identify trends and outliers.
  • Identify Protocol Deviations
  • Produce medical monitor, coding listings and ad hoc listings for team review (Jreview, SAS, Business Objects).
  • Participate in the development and review of clinical study protocols, case report forms (CRFs), and clinical trial documentation.
  • Provide support for regulatory submissions, audits, and inspections related to clinical trial data management.
  • Stay current with industry standards, best practices, and regulatory requirements related to clinical data management.

Qualifications:

  • Bachelor's degree in life sciences, computer science, or a related field. Advanced degree preferred.
  • Minimum of 5 years of experience in clinical data management within the pharmaceutical or biotechnology industry.
  • Proficiency in Medidata Rave electronic data capture (EDC) system..
  • Strong understanding of Good Clinical Practice (GCP) guidelines, regulatory requirements (e.g., FDA, EMA), and industry standards (e.g., CDISC).
  • Excellent communication, organizational, and problem-solving skills.
  • Ability to work effectively in a fast-paced, cross-functional team environment.
  • Attention to detail and commitment to data quality and integrity.

Location: This is a hybrid position with three days per week onsite at our office in Burlington, MA or Redwood City, CA.

MapLight does not accept unsolicited resumes from recruiters, staffing agencies, or search firms.

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