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Senior Clinical Programmer

2 months ago

London, United States Lifelancer Full time

Due to growth we have an immediate need for 2 Senior Clinical Programmers with RAVE experience to join our Global Data Management team in the UK.

The Senior Clinical Programmer position is responsible for providing database development services to ProPharma clients.

Main Responsibilities:

  • Acts as the Lead Clinical Programmer for one or multiple studies.
  • Complete Clinical programmer tasks for assigned studies under minimal supervision according to the study contract and applicable SOPs.
  • Design develop implement maintain and support clinical database systems.
  • Offer technical expertise for internal and external clients.
  • Code test and document databases as per programming standards and clinical validation policies.
  • Program database manipulation and conduct data transfers for clients.
  • Review Data Validation Plans and Case Report Forms as per area of expertise.
  • Add all external data sources such as PK and central lab within the clinical database if integration is requested or required.
  • Serve as programming contact to handle database issues within area of expertise.
  • Support development and implementation of new technologies.
  • Support Information Technology to evaluate new technology upgrades by participating in software change controls.
  • Support development revision and maintenance of core operating procedures and working instructions pertaining to database. development user acceptance testing and change controls.
  • Interface with project team to organize responsibilities and deliverables.
  • Establish effective communication and professional relationships with teams and external vendors.
  • Interface with Clinical Data Management and corporate team to negotiate timelines.
  • Perform administrative tasks within the EDC system such as site and user management URL level reviews and/or approvals and dictionary updates.
  • Follow and influence the development of data standards and strategies pertaining to the standards library.

Necessary Skills and Abilities:

  • Understanding of the principles of ICH GCP and regulatory requirements is essential.
  • RAVE EDC build experience is essent
  • Excellent organizational and analytical skills strong oral and written communication skills and able to work in a high paced timeline driven setting.
  • Minimum BS in a scientific or health related field or equivalent in years of experience.
  • Previous experience as a clinical database developer with at least one year of experience leading a study build.

Lifelancer ( ) is a talenthiring platform in Life Sciences Pharma and IT. The platform connects talent with opportunities in pharma biotech health sciences healthtech data science and IT domains.

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