Senior Clinical Programmer

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

The SeniorClinical Programmer position is responsible for providing databasedevelopment services to ProPharma clients.

MainResponsibilities:

• Acts as the Lead Clinical Programmer for one or multiplestudies.
• Complete Clinical programmer tasksfor assigned studies under minimal supervision according to thestudy contract and applicable SOPs.
• Designdevelop implement maintain and support clinical databasesystems.
• Offer technical expertise forinternal and external clients.
• Code test anddocument databases as per programming standards and clinicalvalidation policies.
• Program databasemanipulation and conduct data transfers forclients.
• Review Data Validation Plans and CaseReport Forms as per area of expertise.
• Add allexternal data sources such as PK and central lab within theclinical database if integration is requested orrequired.
• Serve as programming contact tohandle database issues within area ofexpertise.
• Support development andimplementation of new technologies.
• SupportInformation Technology to evaluate new technology upgrades byparticipating in software change controls.
• Support development revision and maintenance of core operatingprocedures and working instructions pertaining to database.development user acceptance testing and changecontrols.
• Interface with project team toorganize responsibilities and deliverables.
• Establish effective communication and professional relationshipswith teams and external vendors.
• Interfacewith Clinical Data Management and corporate team to negotiatetimelines.
• Perform administrative tasks withinthe EDC system such as site and user management URL level reviewsand/or approvals and dictionary updates.
• Follow and influence the development of data standards andstrategies pertaining to the standardslibrary.

NecessarySkills and Abilities:

• Understanding of the principles of ICH GCP and regulatoryrequirements is essential.
• RAVE EDC buildexperience is essent
• Excellent organizationaland analytical skills strong oral and written communication skillsand able to work in a high paced timeline drivensetting.
• Minimum BS in a scientific or healthrelated field or equivalent in years of experience.
• Previous experience as a clinical database developer withat least one year of experience leading a study build.

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