Senior Clinical Programmer
ProPharma Group, Can be based anywhere
Senior Clinical Programmer
Salary not available. View on company website.
ProPharma Group, Can be based anywhere
- Full time
- Permanent
- Remote working
Posted today, 18 Oct | Get your application in now to be one of the first to apply.
Closing date: Closing date not specified
job Ref: 57c80c4489f042f2a29993d8eead1a8d
Full Job Description
The Senior Clinical Programmer position is responsible for providing database development services to ProPharma clients.,
- 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.
Understanding of the principles of ICH GCP and regulatory requirements is essential. - RAVE EDC build experience is essential.
- 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.