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Senior Associate, Statistical Programming

2+ years
Not Disclosed
10 Dec. 11, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job Title: Statistical Programmer
Location: Remote (Global)
Employment Type: Full-time
Posted: 12/11/2024

About Biorasi:

At Biorasi, we are rapidly expanding, offering an innovative, dynamic, and evolving environment. As an award-winning, customer-focused, full-service clinical research organization, we empower your career growth while promoting work-life balance. We're looking for passionate individuals to join our team—whether you're a clinical trial veteran or new to clinical research. This is your opportunity to be a vital part of a growing global company driving new therapies to patients.

Your Role:

As a Statistical Programmer, you will contribute to creating high-quality outputs that meet project requirements. Key responsibilities include:

  • Creating outputs that meet quality standards and project requirements.
  • Maintaining well-organized, up-to-date project documentation and ensuring inspection readiness.
  • Reading and understanding study documents (Protocol, eCRF, Dataset specifications, SAP, Mock shells) and providing feedback.
  • Contributing to project-specific objectives and team deliverables.
  • Managing on-time delivery of concurrent programming tasks.
  • Developing annotated CRFs and regulatory submission documentation (Define.xml, data reviewer’s guides).
  • Learning to develop programming specifications compliant with client requirements and CDISC standards.
  • Developing and validating CDISC-compliant datasets (SDTM/ADaM) and TLFs, supporting clinical study reports, regulatory submissions, and publications.
  • Maintaining a high level of professionalism, performance, and quality.
  • Undergoing regulatory training (ICH GCP, 21 CFR Part 11) and other related trainings.
  • Other statistical programming duties as assigned.

Your Profile:

  • Education: Bachelor’s Degree in Mathematics/Statistics, Life Sciences, Computer Science, or related field.
  • Experience: At least 2 years of experience in Biostatistics or Statistical Programming within the pharmaceutical industry or a related field.
  • Skills:
    • Ability to multitask and prioritize work with strong attention to detail, timeliness, and quality.
    • Strong problem-solving and leadership skills, capable of contributing creative and practical solutions.
    • Excellent teamwork and communication skills, both written and verbal.
    • Significant knowledge of drug development, clinical research, and ICH GCP guidelines.
    • Ability to work in a fast-paced environment and effectively manage time.

Why Biorasi?

  • Employee Benefits: Half-day Fridays, paid time off, paid holidays, employee bonus programs, career growth, and training opportunities.
  • Diversity and Inclusion: Biorasi is committed to creating a diverse and inclusive environment and is an equal opportunity employer.

Apply Now:

If you're ready to join an energetic, creative, and collaborative team, apply directly on our website at Biorasi Careers or email us at careers@biorasi.com.