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Remote Clinical Trial Data Entry Jobs (NOW HIRING)

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Support the operational strategy related to assigned vendors, data flow, drug supply, remote ...

Civia Health

Clinical Trial Manager

Remote, US East Coast Job Type: Full-Time Reports To: Head of Country Delivery Internal Team Title ... Delivered as planned • Data Entry Timeliness: Within 24-48 hours • Query Aging: ≤7 days • ...

Fortrea

Clinical Trial Manager

Remote US or Canadian based. Job Overview: The Clinical Trial Manager has ownership in the clinical ... Proactive planning for monitoring activities to ensure data integrity, patient safety and endpoint ...

Immatics NV

Clinical Trial Manager

$130K - $150K/yr

Fully Remote Salary Range: $130,000 - $150,000 Basic Qualifications: * Bachelor's degree in life ... Review trial progress, patient recruitment, and data quality metrics, and implement actions to ...

Recursion

Senior Clinical Trial Manager

New York, NY · Remote

$149K - $200K/yr

... data sets, and sophisticated analytics. We are seeking a highly motivated, skilled, and adaptable ... This position is open to both remote and hybrid models. The hybrid position would be office-based ...

IQVIA

Clinical Trial Operations Specialist

Durham, NC · Remote

$68K - $171K/yr

Monitor trial progress, budgets, and system data, identifying risks and implementing corrective ... Fluent in written and spoken English. #LI-Remote #LI-NITINMAHAJAN IQVIA is a leading global ...

New

IQVIA

Clinical Trial Operations Specialist

Durham, NC · Remote

$68K - $171K/yr

Monitor trial progress, budgets, and system data, identifying risks and implementing corrective ... Fluent in written and spoken English. #LI-Remote #LI-NITINMAHAJAN IQVIA is a leading global ...

New

Only Data Entry

Junior Data Entry Operator | Remote

Junior Data Entry Operator | Remote Burbank, California, United States Job Openings Junior Data Entry Operator | Remote About the Job Junior Data Entry Operator | Remote Are you ready to embark on a ...

Only Data Entry

Data Entry Assistant (Junior / Remote)

$17.25 - $22.75/hr

Data Entry Assistant (Junior / Remote) Washington, District of Columbia, United States Job Openings Data Entry Assistant (Junior / Remote) About the Job Data Entry Assistant (Junior / Remote) CHECK ...

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

As of Jul 13, 2026, the average hourly pay for remote clinical trial data entry in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What is the difference between Remote Clinical Trial Data Entry vs Remote Clinical Research Coordinator?

AspectRemote Clinical Trial Data EntryRemote Clinical Research Coordinator
CredentialsHigh school diploma or equivalent; some roles may require certification in clinical data managementBachelor's degree in health sciences or related field; often requires clinical research certifications
Work EnvironmentPrimarily remote, working with electronic data systemsMostly remote or hybrid, coordinating study activities and communicating with teams
Job ResponsibilitiesInputting and managing clinical trial data accuratelyOverseeing study progress, managing documentation, and liaising with stakeholders

While both roles support clinical trials, Remote Clinical Trial Data Entry focuses on data input and management, whereas Remote Clinical Research Coordinator involves broader study oversight and coordination. Understanding these differences helps in choosing the right career path or job search focus.

What cities are hiring for Remote Clinical Trial Data Entry jobs? Cities with the most Remote 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 Remote Clinical Trial Data Entry jobs? States with the most job openings for Remote Clinical Trial Data Entry jobs include:
Remote Clinical Trial Data Entry jobs near you
Clinical Data Manager II/Senior Clinical Data Manager

Clinical Data Manager II/Senior Clinical Data Manager

Precision for Medicine

Remote

Full-time

Medical, Life, Retirement, PTO

Re-posted 8 days ago

Job description

*This position is 100% remote, but the preference is to have someone on the east coast*
Position Summary:
The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position will also oversee and/or perform database development and testing.
Essential functions of the job include but are not limited to:
  • Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s), ensuring that there is back-up, continuity, responsiveness, and that tasks are performed in a timely manner. May support another Lead DM as a back-up and/or team member. May include DM oversight of sponsor programs.
  • Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcing
  • May perform quality control of data entry
  • Provide input, assesses and manage timelines. Ensure that clinical data management deadlines are met with quality. Assess resource needs for assigned projects, as needed.
  • Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders
  • May assist in building clinical databases
  • Conduct database build UAT and maintain quality controlled database build documentation. Oversee overall quality of the clinical database.
  • May specify requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. Oversee development of the edit check specifications and manual data review specifications
  • Responsible for creating, revising, appropriate versioning and maintaining data management documentation. Oversee completeness of data management documentation for the Trial Master File.
  • Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed.
  • Review and query clinical trial data according to the Data Management Plan
  • Perform line listing data review based on the guidance provided by the sponsor and/or Lead DM
  • Run patient and study level status and metric reporting
  • Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency
  • Coordinate SAE/AE reconciliation
  • Liaises with third-party vendors such as external data and EDC vendors in a projectmanager capacity in support of timelines and data-related deliverables
  • May assist with SAS programming and quality control of SAS programs used in the Data Management department
  • Identify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders
  • May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project
  • Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities
  • May attend strategy meetings, bid defense prep meetings, bid defenses, capability presentations, potential client engagement meetings
  • May review Request for Proposals (RFP), proposals, provide project estimates
  • Provide leadership for cross-functional and organization-wide initiatives, where applicable
  • Trains and ensures that all data management project team members have been sufficiently trained
  • Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues
  • May present software demonstrations/trainings, department/company training sessions, present at project meetings
  • May require some travel
  • Perform other duties as assigned
Qualifications
Minimum Required:
  • Bachelors and/or a combination of related experience

Other Required:
  • 8+ years` experience as a Sr. Clinical Data Manager and 5 Years as a Clinical Data Manager II
  • Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
  • Able to handle a variety of clinical research tasks
  • Excellent organizational and communication skills
  • Professional use of the English language; both written and oral
  • Experience in utilizing various clinical database management systems
  • Broad knowledge of drug, device and/or biologic development and effective data management practices
  • Strong representational skills, ability to communicate effectively orally and in writing
  • Strong leadership and interpersonal skills
  • Ability to undertake occasional travel

Preferred:
  • Experience in a clinical, scientific or healthcare discipline
  • Dictionary medical coding (MedDRA and WHODrug)
  • Understanding of CDISC standards (CDASH, SDTM, ADaM, etc....)
  • Oncology and/or Orphan Drug therapeutic experience

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.
Reasonable estimate of the current range
$91,500- $166,100 USD
Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.

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