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Spontaneous Application - Clinical Programming Or Biostatistics

Quanticate
Quanticate
2+ years
Not Disclosed
10 Jan. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Spontaneous Application – Clinical Programming & Biostatistics

Location: Remote, United Kingdom
Department: Clinical Programming / Biostatistics
Employment Type: Full-Time | Remote
Experience Required: 2+ years in clinical programming or biostatistics


Job Summary

Quanticate, a global data-focused Contract Research Organization (CRO), invites applications from experienced professionals in clinical programming and biostatistics. We collaborate with leading pharmaceutical, biotechnology, and medical device companies across all phases of clinical research, from early development to post-marketing studies.

This spontaneous application opportunity is ideal for candidates who want to build a career in biometrics, work with CDISC standards, and contribute to the delivery of high-quality clinical trial data and analysis.

Quanticate offers a supportive, flexible, and development-focused environment, providing exposure to a variety of global projects, cross-functional collaboration, and professional growth opportunities.


Key Responsibilities

  • Support clinical programming or biostatistics activities across multiple therapeutic areas and study phases.

  • Develop, validate, and maintain datasets compliant with CDISC SDTM and ADaM standards.

  • Assist in statistical analyses, outputs, and reporting in line with global regulatory requirements.

  • Collaborate with cross-functional teams, including clinical operations, data management, and statistical teams.

  • Contribute to technical solutions, problem-solving, and workflow optimization.

  • Mentor or support junior team members where appropriate.


Qualifications & Skills

  • Required: Minimum 2 years of experience in clinical programming or biostatistics within pharma or CRO environments.

  • Preferred: Strong knowledge of CDISC standards, statistical methodology, and clinical trial reporting.

  • Proficiency with SAS, R, or Python programming is advantageous.

  • Strong analytical, problem-solving, and organizational skills.

  • Excellent written and verbal communication skills for international collaboration.


Why Join Quanticate?

  • Work remotely with global clinical trial programs.

  • Exposure to diverse projects that enhance technical and domain expertise.

  • Opportunity to collaborate with experienced professionals across clinical programming, biostatistics, and data management.

  • Build a career in a CRO that values quality, innovation, and professional growth.


Benefits

  • Competitive salary based on experience.

  • Remote working allowance and flexible working hours.

  • 25 days annual leave plus UK bank holidays, with the option to purchase additional days.

  • Company-matched pension scheme.

  • Private medical insurance and standard eye test every two years.

  • Employee Assistance Program (EAP) for employees and immediate family.

  • Long-term disability insurance and death-in-service benefits.

  • Service recognition awards at 5, 10, and 15 years.

  • Structured professional development opportunities including mentoring, coaching, e-learning, and job shadowing.


How to Apply

Submit your CV along with a brief summary of your experience and the type of role you are seeking. Quanticate will contact you when a suitable position becomes available.

Apply via Email: careers@quanticate.com