Senior SAS Programmer - Nottingham, United Kingdom - Calyx

Calyx

Verified Company

Nottingham, United Kingdom

1 week ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

About Calyx
We're on a mission to change the future of clinical research. At Calyx, we help the biopharmaceutical industry bring medical treatments to the market, faster.

Our mission is to change the world - but to do this, we need people like you.

What can we offer you?

Apart from job satisfaction, we can offer you:

YOURSELF

Flexible working
25 days' holiday (with the option to buy more)

HEALTH

Simplyhealth Health Cash Plan
Optional private health and dental insurance, and health screens
Cycle to work scheme (Applies to all employees)

WEALTH

Generous pension scheme with up to 10% employer contribution
Life assurance
Season ticket loan

Job Purpose

We are recruiting for a Senior Software Engineer / Senior SAS Programmer to join our growing Data team within Medical Imaging Operations.

The primary role of this position is to create and maintain reports and data exports using SAS in support of clinical trials managed by Medical Imaging.

The reports and exports will be the output sent to clients, data management, and regulatory agencies.
The reports will also be leveraged internally for quality control, outlier identification, billing, and medical QC.

You will work to enhance the group's reporting and export capabilities and implement solutions in a consistent manner.

The analyst will be exposed to the development of standard reports in the various systems that support trial operations while leveragingSQL, SAS, Python and PowerBI.

Role Responsibilities

Development of trial exports, reports (outlier, QC, etc.), and reconciliation reports while working closely with Validation Engineers to complete project validation.
Development of standard and custom reports leveraging SAS and SQL.
Write and implement Installation Qualifications for deployment and running of reports and exports within the testing and production environments.
Assist in developing QC procedures to identify data anomalies.
Assist in creating deployment standards and configurations that support automated integration points.
Contributes to selection of the software development approach for projects, selecting appropriately from predictive (plandriven) approaches or adaptive (iterative/agile) approaches.
Applies agreed standards and tools, to achieve wellengineered outcomes. Participates in reviews of own work and leads reviews of colleagues' work. Applies data analysis, design, modelling, and quality assurance techniques, based upon a detailed understandingof business processes, to establish, modify or maintain data structures and associated components (entity descriptions, relationship descriptions, attribute definitions).

Essential Skills and Experience

Extensive SAS programming experience
SQL experience within Oracle, DB2 or SQL Server
A flexible attitude with respect to work assignments and new learning
Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
Plans own work to meet given objectives and processes
Experience within a clinical trials / life sciences setting would be helpful but not essential