The Role :
The Senior Clinical Programmer (SCP) plays a pivotal role in supporting clinical research by developing, validating, and maintaining statistical programs and datasets. Collaborating with Biostatisticians, Clinical Data Managers, and cross-functional teams, the Senior Clinical Programmer ensures high-quality, timely deliverables that meet regulatory standards and study objectives. This role requires advanced SAS programming expertise, strong problem-solving skills, and the ability to mentor junior team members.
The SCP should thoroughly understand the requirements for Good Clinical Data Management services, including its documentation; be willing to be involved in start-up or wrap-up of in-house and client-specific data management projects; have an understanding of the relevant therapeutic indications, study hypotheses, and trial design; and have a solid understanding of database design and structure.
ESSENTIAL FUNCTIONS
- Program customized data displays, (including data listings, summary tables and routine graphics) in accordance with the approved statistical analysis plan (SAP) and shell displays for clinical research studies.
- Analyze protocol, SAP, existing shells / templates as needed to understand structure and content of data.
- Prepare documentation for programs
- Prepare documentation describing all datasets and variables within, including derived variables, and the project as a whole.
- Create SAS datasets of clinical data from clinical databases
- Create status and efficacy datasets
- Create project-specific macros and formats
- Create study reports using SAS or Program R
- Load client data from other platforms and other software packages
- Prepare data to be sent to clients and as needed for other external transfers and data imports.
Ideal Profile :
QUALIFICATIONS FOR ESSENTIAL FUNCTIONS
Ability to communicate effectively in the English language in person, by phone and in writing.Ability to lead functional meetings.Strong attention to detail and accuracy is a must.Excellent organizational skills.Demonstrated ability to manage multiple projects.Ability to work collaboratively, effectively, and productively in diverse organization structures.Ability to work independently, take initiative and complete tasks to deadlines : Delivering Excellence, Serving Customers, Accountability and Ownership, Global and Cross-Functional Communication.Ability to work in a team-oriented, collaborative environment.Ability to work positively within a continually changing environment.Ability to effectively prioritize and execute tasks in a high-pressure environment.Advanced computer skills and practical knowledge of MS Office and potentially project management software.EDUCATION AND EXPERIENCE REQUIRED
A Bachelor’s degree or equivalent combination of Education / Training / Experience is required. A degree in a scientific, medical, or technological discipline is preferred.A minimum of 3 years of clinical trial or clinical data management experience or similar industry experience / training is required.Prior trial responsibility for the entire data management life-cycle is desirable.Working knowledge of EDC studies is required and SAS is preferred.WORK REQUIREMENTS
1. Cross-functional interactions.
TRAINING
Complete Training Requirements per current Training Requirements List.Supervisor may assign additional skills training, one-on-one, see-one / do one, or other Training as necessary to achieve qualifications and improve job performance.What's on Offer?
Work alongside & learn from best in class talentJoin a well known brand within Hospital / Health Care / HealthtechFlexible working options