Company description
Smart Tech Sol is a technical consultancy solving complex problems with technology. We connect strategy and execution, helping our clients to strengthen their core technology, scale with flexibility and create seamless digital experiences. We partner with our clients to continuously evolve their tech and enable an adaptive mindset to meet their business goals.
Job description
Clinical Data Programming Lead
We are seeking an experienced Clinical Data Programming Lead to join our clinical data programming team. This role will take responsibility for planning, coordinating and delivering clinical programming activities, ensuring high-quality and compliant clinical data deliverables throughout the study lifecycle.
Key Responsibilities
The successful candidate will:
- Plan and work closely with the clinical programming group to schedule specification, programming, validation and ongoing delivery activities.
- Write and execute SAS programs to produce internal and sponsor deliverables.
- Lead timelines associated with the programming setup process, ensuring issues are identified, addressed and resolved appropriately.
- Produce clinical data delivery validation packages for study teams for filing within the Trial Master File (TMF).
- Participate in specification reviews, program validation and quality assurance activities relating to study data deliverables.
- Apply specialist clinical programming knowledge and experience to support clinical data programmers assigned to clinical studies.
- Ensure programming and clinical data deliverables are produced accurately, efficiently and in accordance with applicable processes and quality requirements.
- Participate in sponsor audits and present the Clinical Data Delivery process and procedures from a compliance perspective.
- Work collaboratively with study teams and other stakeholders to support successful clinical study delivery.
Skills and Experience
We are looking for candidates who can demonstrate:
- Strong experience in clinical data programming within a clinical research, pharmaceutical or related environment.
- Strong SAS programming knowledge and practical programming experience.
- Experience with programming specifications, validation and quality assurance.
- Experience coordinating programming activities and managing delivery timelines.
- Understanding of clinical study data deliverables and associated documentation.
- Knowledge of quality and compliance requirements within a regulated clinical research environment.
- Ability to support and provide technical guidance to other clinical data programmers.
- Strong attention to detail, analytical and problem-solving skills.
- Effective communication and stakeholder-management skills.
- Ability to work collaboratively within multidisciplinary clinical study teams.
Working Hours
37.5 hours per week
Employment
Full-time
This is an excellent opportunity for an experienced clinical data programming professional to take a lead role in the planning, programming, validation and quality assurance of clinical study data deliverables while working closely with clinical programming and study teams.
How to Apply
Please submit your CV together with a brief summary of your relevant clinical data programming experience, including your experience with SAS programming, validation, quality assurance and clinical study deliverables.
Apply now!
Job Type: Full-time
Pay: £55,000.00-£61,000.00 per year
Benefits:
- Company events
- Cycle to work scheme
- On-site parking
- Referral programme
- Sick pay
- Work from home
Education:
Experience:
Work Location: In person
