Senior Programmer (Remote)

Senior Programmer | Clario | United States

Senior Clinical Data Programmer page is loaded **Senior Clinical Data Programmer** locations United Kingdom Remote time type Full time posted on Posted 16 Days Ago job requisition id R15268 Clario is expanding its Digital Physiology team in the UK and is looking for a Senior Clinical Data Programmer.

In this role, you’ll develop and test SAS code, review data specifications, and collaborate with Data Managers to ensure accurate data file creation. You’ll also be involved in program validation, quality control, and ad-hoc programming tasks, while contributing to process improvements and becoming a Subject Matter Expert (SME) in key offerings. Join us to help drive innovation in healthcare through high-quality data solutions.

**What we offer**

* Competitive compensation

* Attractive benefits (security, flexibility, support and well-being)

* Remote working with full technology setup

**What you’ll be doing**

* Create and test SAS code used for standard and non-standard data file creation

* Review Clario standard and non-standard data specifications

* Attend client meetings as appropriate to understand data collection requirements.

* Review standard CLARIO and non-standard data specifications and interact with the Data Manager (DM) to finalize specifications.

* Develop programs to create Clario standard and non-standard data files.

* Participate in the validation of encoding programs which generates CLARIO standard and non-standard data files.

* Performing ad-hoc programming activities utilizing raw data based on internal and external requests for

a. Esoteric quality control checks requested by QC.

b. Data resolution/Mining.

c. Other client requirements.

* Get exposed to all modalities and become a Subject Matter Expert (SME) on our top 5 offerings.

* Review User Requirements and create, review and approve Functional and Technical Specifications.

* Work with data management in providing programming support for DM activities including data review.

* Prepare and participate in internal and external audits. Represent the service line through the NPI process.

* Identify opportunities to improve the methodology and provide practical solutions for problems.

* Contribute to the development of best practices to improve quality, efficiency and effectiveness.

* Drive client deliverables by performing the role of CDP SME when attending Project Management, Data Management or CDO meetings.

* Assist with orientation and training of personnel as determined by management.

* Contribute to process development.

* Review and development of SOPs and associated documents related to Clinical Data Programming activities.

* Complete administrative tasks as needed within Clinical Data Programming. Mentoring other Clinical Data Programming resources

**What we look for**

* BS/BA Degree in Life Sciences or BS/BA Degree in computer sciences or related field

* SAS ADVANCED certified

* Ideally ten or more years of experience in a pharmaceutical company or a CRO as a SAS Programmer – experience in SAS/BASE, SAS/MACRO and SAS/SQL products and procedures and one or more years of experience in database design and data structures

* Understanding of the pharmaceutical drug development process, as gained through a minimum of five years of experience in the pharmaceutical or healthcare industry.

* Strong organization, analytical and communication skills.

* Detail-oriented

* Extensive experience in implementing CDISC SDTM and Define standards including EG, CO, DM, RE, VS, SUPP CDISC SDTM domains.

* Experience with Windows and Microsoft Office products preferred.

* Strong written and verbal communication skills.

* Fluency in English (spoken and written).

* Experience with another programming languages is a plus.

* Proven experience working with large, complex real-world data sets (more specifically, patient data)

* Knowledge of technical and regulatory requirements related to the role.

* Excellent time management skills, contributing to multiple projects with competing timelines.

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.

Clario is committed to providing an inclusive workplace that welcomes diversity and equal opportunity. We encourage all qualified candidates who are passionate about sustainability, ethical business, and making a positive impact to apply for this role.

Clario delivers the leading endpoint technology solutions for clinical trials. Through experience gained from over 19,000 clinical trials delivered in support of 870 regulatory approvals, Clario fuses scientific expertise and global scale into the broadest endpoint technology platform to enable pharmaceutical, biotech and medical device partners to transform lives. Through Trial Anywhere™, Clario has mastered the ability to generate rich evidence across all trial models: decentralized, hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe and Asia Pacific, Clario’s global team of science, technology and operational experts has been delivering the richest clinical evidence for nearly 50 years.