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Clinical Data Programmer

Lifelancer
United Kingdom only
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We are looking for a Clinical Database Programmer who would be responsible for overseeing all technical aspects of clinical data management activities across multiple clinical trials and programs.

Their duties range from evaluating, developing, and maintaining study specific Clinical Data Management Systems, through coding, testing, and performing data validation, to developing algorithms to support clinical data management activities.

The Clinical Database Programmer is passionate about clinical research and a commitment to quality to make a significant contribution to the success of clinical trials.


Duties And Responsibilities

  • Oversee/execute database lock requests.
  • Design, develop, implement, maintain and support internal and external study specific clinical data management systems
  • Review database specification documents, such as CRF Specifications and Data Validation Specifications (DVS)
  • Create/Program edit checks, special actions and derivations as per a DVS
  • Program database manipulation to facilitate conduct of data transfer
  • Offer technical expertise for Clinical Data Managers and serve as programming contact to handle study specific database issues
  • Complete study database updates as specified per Change Request documents and procedures
  • Trouble-shoot and solve study building issues and edit check programming issues
  • Validate clinical data programs per the formal, documented QC process
  • Support development, revision, implementation and maintenance of core CDM strategies processe,s operating procedures and working instructions
  • Participate and contribute towards internal CDM group meetings to share knowledge and provide latest updates/features
  • Participate in Clinical Data Management department initiatives
  • Ensure CDM activities conform to ICH GCP guidance
  • Establish effective communication and maintain productive working relationships with Engineering and other Service delivery teams to ensure seamless end-to-end data flow of clinical trial data

Qualification needed

What we need from you

  • Bachelors degree in a relevant field (i.e. Life Sciences, Engineering, etc)
  • Certificate in Good Clinical Precise (GCP)
  • Experience in programming (SAS, SQL, Python, R, etc.)
  • Knowledge of effective clinical data management practices
  • Experience working with Clinical Data Management and Electronic Data Capture (EDC) systems.

We recommend applying via the Lifelancer website at the below link for quicker response.

https://lifelancer.com/jobs/view/ae359c167e05d4f6c17f02323cddfbd6

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About the job

Apply before

Aug 10, 2024

Posted on

Jun 11, 2024

Job type

Full Time

Experience level

Senior

Location requirements

Hiring timezones

United Kingdom +/- 0 hours
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