Data Analysis Expert for Pharmaceutical Industry
5 days ago
As a mid-size Contract Research Organisation (CRO), Veramed is dedicated to providing top-notch statistics and programming consultancy to its clients, while offering an exceptional working environment, comprehensive support, and opportunities for growth. Unlike other organisations, we don't subscribe to a one-size-fits-all model for our Programmers, which is why you'll find unique responsibilities, daily interactions, and opportunities for each Programmer type we're hiring for on our Programmer careers page.
The core role of the SAS & R Programmer involves delivering statistical support to the statistics and programming department across various projects, clients, and therapeutic areas. Understanding each Programmer type can help you chart a clear career path and work in a role suited to your skills and personality – whether it's as a Portfolio Lead, a Delivery Programmer, or a mix of many Programmer types. Let's find the right fit for YOU, not just your CV.
We are seeking an experienced Programmer with a flair for computing environments and programming languages or deep knowledge of technical data standards. The ideal candidate should also possess excellent communication skills, the ability to advise and demonstrate effective communication with team members and stakeholders.
KEY RESPONSIBILITIES:
This role entails a wide variety of responsibilities and client exposure – you are certainly not pigeon-holed.
Below is a range of the types of tasks you could be carrying out on a daily basis. As with many roles at Veramed, you have the opportunity to shape their direction dependent on client needs and your own career aspirations.
PROGRAMMING:
- Support the specification, development, validation, delivery, and adoption of SAS & R tools and techniques following the software development lifecycle (SDLC) as applied to clinical trials.
- Provide technical expertise to support the delivery teams.
- Validation and oversight of biostatistics platforms and tools and the creation and maintenance of associated documentation.
DAILY INTERACTIONS:
- Act as the subject matter expert (SME) in the business, providing technical insight and consultancy.
- Share technical and wider industry knowledge (including clinical trial, therapeutic area, and scientific context) with the client study teams and internal colleagues.
OPPORTUNITIES FOR:
- Presenting at conferences.
- Contributing to business process improvements and authoring/presenting internal training.
- Providing significant contributions to internal Hackathons.
- Contributing to initiatives that consider employees, the environment, and our local communities as part of our B Corp accreditation.
- Maximising knowledge sharing across the industry.
WHAT TO EXPECT:
- A warm, friendly working environment where you can thrive both personally and professionally.
- A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level.
- Exposure to a wide range of clients and projects, allowing you to diversify your workload and work closely with some of the biggest pharma companies in the industry.
- Work with a truly unique CRO that's doing something different when it comes to managing staff, projects, and building relationships in the industry.
- The ability to truly own your role and develop your skills and experience.
BENEFICIAL EXPERIENCE:
- Excellent verbal and written communication skills with the ability to vary style and level and adapt to different working styles to understand needs of stakeholders.
- Completer-finisher abilities with a high attention to detail.
- Ability to translate strategy and elicited needs into practical project implementation and delivery.
- Understanding of data standards conformance and compliance.
- Excellent problem-solving abilities.
SALARY: The estimated annual salary for this position is £50,000 - £70,000, depending on qualifications and experience.
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