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Senior/Principal Statistical Programmer, Pk/Pd

2+ years
$130-140K
10 Sept. 4, 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: Senior/Principal Statistical Programmer, PK/PD

Responsibilities:

As a Senior/Principal Statistical Programmer specializing in PK/PD, you will be crucial in designing, executing, and analyzing clinical trials to support the development of innovative drug candidates. Your role involves:

  • Applying advanced statistical programming techniques using SAS, R, or other relevant languages to analyze PK/PD data.
  • Collaborating with cross-functional teams, including scientists, clinical researchers, and biostatisticians, to ensure effective implementation of clinical development programs.
  • Utilizing your expertise in PK/PD principles to contribute to modeling and simulation efforts.
  • Ensuring compliance with clinical trial designs, protocols, and regulatory requirements specific to PK/PD endpoints.
  • Adhering to industry standards such as CDISC data structures and guidelines for data submissions.
  • Delivering high-quality results with attention to detail and effective problem-solving skills.

Requirements:

  • Extensive experience in statistical programming within the pharmaceutical or biotech industry, with proficiency in SAS, R, or similar programming languages.
  • Proven expertise in PK/PD data analysis, including modeling and simulation.
  • Solid understanding of clinical trial designs, protocols, and regulatory requirements related to PK/PD endpoints.
  • Familiarity with CDISC data structures and data submission guidelines.
  • Strong analytical, problem-solving, and communication skills, with the ability to work effectively in cross-functional teams.
  • Master’s or Ph.D. in Biostatistics, Statistics, or a related field with a focus on pharmacokinetics (PK) and pharmacodynamics (PD).
  • Ability to manage tight timelines and deliver high-quality outputs.

Compensation:

  • Base salary range: $130,000 - $140,000
  • Final salary offer based on relevant experience, skills, and qualifications.

About Clinovo:

Clinovo empowers healthcare and life science companies by providing top-tier clinical research professionals for diverse opportunities. With a proven track record in pharmaceuticals, biotechnology, diagnostics, medical devices, and CROs, Clinovo is a trusted partner known for exceptional customer service and quality candidates.

Equal Opportunity Employer:

Clinovo is committed to providing equal employment opportunities and prohibits discrimination and harassment of any kind.