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Biostatistician Ii - Fsp

0-2 years
Not Disclosed
10 Nov. 18, 2025
Job Description
Job Type: Full Time Remote 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

Biostatistician II – FSP (Remote, India)

Location: India (Remote)
Job Type: Full-Time, Regular
Experience Required: Fresher – 2+ years


About Parexel

Parexel is a global leader in clinical research services, providing end-to-end support across clinical trials and drug development. As part of Parexel’s Biostatistics team, you will contribute to designing and analyzing clinical trials that ensure the safety and efficacy of new therapies. We offer a flexible, inclusive, and collaborative work environment where professionals can grow and make a tangible impact on global health outcomes.


Role Overview

The Biostatistician II – Functional Service Provider (FSP) will be responsible for applying statistical methods and data analysis to support clinical research. This role involves designing analytical strategies, developing statistical analysis plans (SAPs), producing statistical outputs, and ensuring the highest quality in all deliverables. Freshers with strong statistical knowledge and interest in clinical research are encouraged to apply.


Key Responsibilities

Operational Execution

  • Produce and quality check datasets and statistical outputs, including both simple and complex analyses using SAS or other statistical tools.

  • Apply moderately advanced statistical methods to clinical data, ensuring accuracy and compliance with regulatory standards.

  • Coordinate and lead project tasks to ensure timely delivery within budget.

  • Serve as a key point of contact for clients regarding statistical and contractual aspects.

  • Contribute to the development of analysis plans, statistical reports, and integrated clinical reports.

  • Ensure first-time quality in all deliverables through ongoing checks.

  • Provide statistical training and mentoring to internal teams.

  • Participate in process improvement initiatives to enhance quality and efficiency.

  • Attend and actively contribute to client meetings, including analysis discussions and presentations of study results.

General Activities

  • Mentor and train junior biostatisticians.

  • Perform additional tasks as assigned by supervisor or manager.

Business Development Support

  • Assist in bid defenses and other business development activities as needed.


Required Skills & Competencies

  • Strong analytical and problem-solving abilities.

  • Excellent project management and organizational skills.

  • Detail-oriented with a professional attitude.

  • Good understanding of statistical concepts in clinical trials.

  • Prior exposure to SAS programming or other statistical software is desirable.

  • Ability to work independently and collaboratively in a team.

  • Mentoring and leadership skills for guiding junior team members.


Educational Requirements

  • PhD in Statistics or related discipline – Fresher-friendly

  • MS in Statistics or related discipline with academic or internship experience is acceptable.

  • Knowledge of pharmacokinetic data is advantageous.

  • Proficiency in English (written and oral) is required.


Experience

  • Fresher-friendly: Suitable for candidates with minimal professional experience in clinical research or biostatistics.

  • Academic projects, internships, or research exposure in clinical trials will be considered a plus.


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