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- Tasks: Join us as a Senior Clinical Programmer, managing data for exciting clinical trials.
- Company: Parexel is a leading provider of clinical research services, partnering with top biotechs and pharma companies.
- Benefits: Enjoy job security, professional growth, and a supportive work environment with flexible hours.
- Why this job: Tackle meaningful challenges in clinical studies while maintaining a healthy work-life balance.
- Qualifications: Bachelor’s degree in relevant fields and 5+ years of clinical programming experience required.
- Other info: Opportunities for skill development and career advancement within Parexel.
The predicted salary is between 43200 - 72000 £ per year.
Parexel is currently seeking a Senior Clinical Programmer to join us in the UK, dedicated to a single sponsor. This role will be responsible for the provision of data review and trial management deliverables across all compounds and trials for which these are required, and for all functional groups that require those deliverables. Working as a Senior Clinical Programmer at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. Expect exciting professional challenges in inspiring studies, but with time for your outside life.
Responsibilities
- Program simple to complex data review listings, exception reports, QTL/KRIs, metrics reports and visualizations in a fast-paced environment for clinical trial data review and management purposes.
- Liaise with Clinical Data Management and/or cross functional staff to understand the needs of the end users of the listings, reports, and metrics.
- Contribute to the development of software systems and related infrastructure to generate displays of clinical study data and metrics reports that are efficient and user-friendly.
- Create and document archives of software and deliverables.
- Create any Work Instructions process and training documents needed related to clinical programming and the required deliverables.
- Provide time and resource estimates for project planning as well as accurately record time spent on multiple deliverables.
Requirements
- Bachelor’s degree in computer science, Statistics, Mathematics, Life Sciences or other relevant scientific fields.
- Minimum of 5 years of experience in developing software in a clinical trial environment using SQL, including at least 3 years of clinical programming experience.
- Skilled in programming in a relational database setting with SQL and/or T-SQL or ETL.
- Experience with data reporting tools in a clinical trial setting.
- Experience in the Biotechnology, Pharmaceutical, or Life Sciences industries (Clinical Research Organization - CRO or Clinical Trial regulated environment preferred).
- Experience with the eClinical Solutions elluminate platform a plus; experience with Qlik Sense a plus.
- Preferred additional external data transfer experience in:
- Creating external data transfer specifications, ensuring external clinical trial data are compatible with the clinical database to support data integration, analysis and reporting.
- Experience in planning, set-up, and acquisition of external clinical data at the study level.
- Liaising with and reviewing work delivered by external partners (e.g. laboratories, eCOA providers, technology providers, etc.).
We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.
Who are Parexel
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients. You’ll be an influential member of the wider team.
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Senior Clinical Programmer (FSP) - UK employer: Parexel International
Contact Detail:
Parexel International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Programmer (FSP) - UK
✨Tip Number 1
Familiarise yourself with the eClinical Solutions elluminate platform and Qlik Sense, as these tools are highly valued in this role. Having hands-on experience or even a basic understanding can set you apart from other candidates.
✨Tip Number 2
Network with professionals in the Biotechnology and Pharmaceutical industries, especially those who work in clinical programming. Attend relevant conferences or webinars to make connections that could lead to job opportunities at Parexel.
✨Tip Number 3
Brush up on your SQL and T-SQL skills, as well as your knowledge of CDISC standards like CDASH and SDTM. Being able to demonstrate your technical expertise during interviews will greatly enhance your chances of landing the job.
✨Tip Number 4
Prepare to discuss your experience with external data transfers and how you've liaised with external partners in previous roles. This practical experience is crucial for the responsibilities outlined in the job description.
We think you need these skills to ace Senior Clinical Programmer (FSP) - UK
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical programming, particularly with SQL and data reporting tools. Emphasise your familiarity with the Biotechnology or Pharmaceutical industries, as well as any experience with eClinical Solutions or Qlik Sense.
Craft a Strong Cover Letter: In your cover letter, express your passion for clinical programming and how your skills align with the responsibilities outlined in the job description. Mention specific projects or experiences that demonstrate your ability to manage complex data review listings and liaise with cross-functional teams.
Showcase Technical Skills: Clearly list your technical skills, including programming languages and tools you are proficient in, such as SQL, T-SQL, SAS, or Python. Highlight any experience with CDISC standards and external data transfer specifications, as these are crucial for the role.
Proofread Your Application: Before submitting your application, thoroughly proofread your CV and cover letter for any spelling or grammatical errors. Ensure that your communication is clear and professional, reflecting the strong verbal and written communication skills required for the position.
How to prepare for a job interview at Parexel International
✨Showcase Your Technical Skills
Be prepared to discuss your experience with SQL and other programming languages relevant to the role. Highlight specific projects where you've successfully developed software in a clinical trial environment, as this will demonstrate your capability to handle the technical demands of the position.
✨Understand the Company and Its Clients
Research Parexel and its role in the clinical research industry. Familiarise yourself with their partnerships and the types of studies they conduct. This knowledge will help you articulate how your skills align with their mission and the needs of their clients.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities in real-world scenarios. Think of examples from your past experiences where you had to balance multiple assignments or respond to ad hoc requests, and be ready to explain your thought process and outcomes.
✨Emphasise Communication Skills
Since the role involves liaising with various teams, it's crucial to demonstrate your verbal and written communication skills. Prepare to discuss how you've effectively communicated complex data findings to non-technical stakeholders in previous roles.
