About the role
Join a team that's going places!
Every member of Celerion is involved in making a distinctive contribution to the health and well-being of people around the world. That's the sense of purpose shared by our employees. We are a performance-driven drug research company, operating in robust and growing markets. We have an exciting future and offer a strong development environment for our great employees.
Come be part of our Data Management and Biometrics team as a Data Programmer.
This full-time position will be attached to our Belfast, Northern Ireland clinical trial facility with a work-from-home/hybrid working arrangement available within the UK.
The purpose of the Data Programmer role is to develop and support clinical database programming activities and associated documentation involved in clinical trial set-up, conduct and close-out stages in line with protocol requirements, standard operating procedures (SOPs/PGs), Good Clinical Programming Practices (GXP), Clinical Data Interchange Standards (CDISC) and other applicable sponsor or regulatory requirements.
Essential Functions:
SAS Pre-lock programming - Deliver and support all pre-database lock SAS programming processes associated with data collection, reporting and cleaning
Data import and integration - Support data import programming and reconciliation activities as needed
Data transfer programming - Deliver and support raw/CDASH, lab only, CDISC/SDTM or sponsor specified custom data transfers
Process Improvements - Actively participate in process improvement initiatives
Quality/timelines - Ensure that data programming delivers quality outputs on time or better following good programming practices, including adequately-documented SAS code
This full-time position has an attractive salary and benefits package including pension, life assurance, permanent health insurance and private medical insurance.
Training will be provided on clinical research data programming skills.
Education and Skill requirements
Bachelor's degree with 1+ yrs programming experience OR comparable experience in related industry, previous experience with SAS and clinical data preferred.
Computer science, Mathematics or IT graduate applicants also considered.
Demonstrated communication and interpersonal skills
Demonstrated problem solving and decision making skills
Demonstrated ability to manage multiple priorities
Internal Celerion candidates with strong clinical data review, data management or IT background will also be considered.
Celerion are an equal opportunities employerFind Jobs in United Kingdom on Arbeitnow
Every member of Celerion is involved in making a distinctive contribution to the health and well-being of people around the world. That's the sense of purpose shared by our employees. We are a performance-driven drug research company, operating in robust and growing markets. We have an exciting future and offer a strong development environment for our great employees.
Come be part of our Data Management and Biometrics team as a Data Programmer.
This full-time position will be attached to our Belfast, Northern Ireland clinical trial facility with a work-from-home/hybrid working arrangement available within the UK.
The purpose of the Data Programmer role is to develop and support clinical database programming activities and associated documentation involved in clinical trial set-up, conduct and close-out stages in line with protocol requirements, standard operating procedures (SOPs/PGs), Good Clinical Programming Practices (GXP), Clinical Data Interchange Standards (CDISC) and other applicable sponsor or regulatory requirements.
Essential Functions:
SAS Pre-lock programming - Deliver and support all pre-database lock SAS programming processes associated with data collection, reporting and cleaning
Data import and integration - Support data import programming and reconciliation activities as needed
Data transfer programming - Deliver and support raw/CDASH, lab only, CDISC/SDTM or sponsor specified custom data transfers
Process Improvements - Actively participate in process improvement initiatives
Quality/timelines - Ensure that data programming delivers quality outputs on time or better following good programming practices, including adequately-documented SAS code
This full-time position has an attractive salary and benefits package including pension, life assurance, permanent health insurance and private medical insurance.
Training will be provided on clinical research data programming skills.
Education and Skill requirements
Bachelor's degree with 1+ yrs programming experience OR comparable experience in related industry, previous experience with SAS and clinical data preferred.
Computer science, Mathematics or IT graduate applicants also considered.
Demonstrated communication and interpersonal skills
Demonstrated problem solving and decision making skills
Demonstrated ability to manage multiple priorities
Internal Celerion candidates with strong clinical data review, data management or IT background will also be considered.
Celerion are an equal opportunities employerFind Jobs in United Kingdom on Arbeitnow
Requirements
- Clinical Data Sciences