Data Entry – Clinical Trials

Data Entry Jobs UK, Clinical data entry associates are responsible for collecting information about patients’ medical histories and clinical trials. Speed, accuracy, and attention to detail are requirements listed in a data entry associate job description.

If you are considering working as a clinical data entry associate, you have several options to approach this career. Some employers even allow their employees to work from home, making this an appealing job opportunity for stay-at-home parents.

Clinical data entry associates work with computerized patient records and clinical trial data to ensure it is precisely sorted and recorded. In addition to inputting data, associates might transcribe and code information according to the employer’s specifications. If a record requires more investigation, the associate will retrieve the information for the research team to assess for completeness, accuracy, and errors. 

Job Details

Hiring Organization hVIVO Services Limited
Post Name Data Entry – Clinical Trials
Qualification Any Graduate
Industry Private
Employment Type Full Time
Work Hours 8 Hours
Salary GBP 25000 To GBP 30000 Per Year
Location London, England, United Kingdom E1 2AX

About Organization

Established as a spin-out from Queen Mary University, London, hVIVO part of Open Orphan plc are a trusted partner and industry-leading clinical development services, pioneering in human challenge studies. hVIVO’s clinical trial platform can help accelerate drug and vaccine development in respiratory and infectious diseases.

hVIVO, formally known as Retroscreen, has an extensive history of conducting & running clinical trials, which has aided in its strong position as a world leader in clinical trial research and execution.

hVIVO opened its laboratory, screening, and 24-bedroom quarantine facilities to Queen Mary BioEnterprises in Whitechapel, London. the quarantine facilities expanded to a 19-bedroom hotel, offering volunteers a state-of-the-art clinical trial experience.


  • Work with complex computerized records systems and maintain security and integrity.
  • Collect data from clinical trials.
  • Sort information and then ensure it’s screened, grouped, summarized, transcribed, and coded.
  • Consult with other employees to solve operational or data problems.
  • Provide clerical duties such as data entry, transcription, coding, and collating searches.
  • Prioritize work in line with project management decisions.
  • Manage clinical trials through review, computerization, cleaning, and auditing of clinical data and databases in compliance with standard operating procedures, client guidelines, and regulatory agency guidelines.
  • Validate clinical trial data to ensure consistency, integrity, and accuracy based on project-specific guidelines.
  • Generate data retrievals and summaries.

Skills & Requirements

  • Complete secondary school. The minimum requirement to start a career in data entry is your GED or high school diploma. 
  • Consider a certification program. 
  • Improve your typing skills. 
  • Learn more software.
  • Apply for a role.
  • Easy to learn. 
  • Ample opportunities. 
  • Flexible work options.


  • Flexible working schedule. Data entry jobs offer a bigger advantage of working according to your specifications. 
  • Payment against entry.
  • Low level of stress.
  • Improves skills. 
  • Improves communication skills. 
  • The process to Identify fraudulent Data Entry Organizations.

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