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Experienced Biostatistician

0-2 years
Not Disclosed
10 Feb. 12, 2025
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: Experienced Biostatistician

Location: Hyderabad, India
Department: Biostatistics
Job Type: Full-time, Permanent


ABOUT MEDPACE

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace operates in 40+ countries with over 5,000 employees.

Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach, leveraging local regulatory and therapeutic expertise in key areas such as oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective research.


JOB SUMMARY

We are seeking a full-time Biostatistician to join our Biometrics team in Hyderabad. The role will involve working in a team environment to contribute to the design, execution, and analysis of clinical trials. This is an excellent opportunity to apply previous expertise, develop advanced skills, and grow within a global organization.


KEY RESPONSIBILITIES

Clinical Development & Study Design

  • Contribute to clinical development plan preparation.
  • Review study protocols and develop statistical methodologies.
  • Prepare detailed Medpace Data Analysis Plans for assigned projects.

Data Analysis & Statistical Reporting

  • Program study analysis, review results, and prepare the statistical methods section for clinical/statistical reports.
  • Generate analysis databases and perform statistical analyses for medium-to-high complexity clinical trial projects, including ISS, ISE, and electronic submissions.
  • Communicate statistical results to medical writing personnel for accurate interpretation.

Collaboration & Regulatory Compliance

  • Work with teams on CRF design, database design, and database cleanup to ensure key study variables are suitable for analysis.
  • Ensure compliance with regulatory requirements/guidelines for drug development.
  • Stay updated on complex statistical methods applicable to Phase I-IV clinical trials.

QUALIFICATIONS & EXPERIENCE

Education:

  • Ph.D. in Biostatistics/Statistics with experience in pharmaceutical clinical trials.

Technical Skills:

  • Strong experience in SAS® programming or equivalent statistical software.
  • Knowledge of advanced statistical methods used in the pharmaceutical industry.
  • Familiarity with statistical software beyond SAS.
  • Experience with data analysis, ISS, ISE, and electronic submissions.

Soft Skills:

  • Excellent verbal and written communication skills.
  • Strong team collaboration and problem-solving abilities.

WHY JOIN MEDPACE?

Work Environment & Benefits

  • Hybrid work-from-home options (dependent on position and level).
  • Competitive PTO packages.
  • Company-sponsored employee appreciation events.
  • Health and wellness initiatives.
  • Flexible work schedules.
  • Competitive compensation and benefits.
  • Structured career paths with opportunities for professional growth.

Awards & Recognition

  • Forbes "America's Most Successful Midsize Companies" (2021-2024).
  • Recognized with CRO Leadership Awards for expertise, quality, capabilities, reliability, and compatibility.

HOW TO APPLY

If you are passionate about biostatistics and clinical research, apply now to be part of Medpace’s mission to improve lives through medical innovation.