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Associate Scientist, Qpp/Scientist, Qpp/Clinical Pharmacology

Cytel
Cytel
3-5 years
Not Disclosed
10 April 17, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

Associate Scientist / Scientist – QPP / Clinical Pharmacology (6-Month Contract)
Location: India (Ahmedabad / Pune / Remote)
Contract Duration: 6 Months
Experience Required: 3–5 Years
Job Type: Full-Time, Contract
Department: Clinical Pharmacology
Company: Cytel
Job ID: 541
Posting Date: April 3, 2025


Position Overview

Cytel is seeking a full-time Consultant for a 6-month contract role within the Quantitative Pharmacology and Pharmacometrics (QPP) group. The successful candidate will focus on non-compartmental pharmacokinetics (PK) analyses, quality control (QC), and programming support. This is a great opportunity for a professional with a background in pharmacokinetics and data science to contribute to high-impact clinical development programs.


Required Qualifications

  • Bachelor’s or Master’s degree in Pharmacy, Biology, Chemistry, Data Science, or a related scientific field.

  • 3–5 years of relevant experience in the pharmaceutical industry.

  • Basic understanding of pharmacokinetics principles.

  • Proficiency in R programming.

  • Experience with WinNonlin is strongly preferred.


Key Responsibilities

  • Conduct and perform QC of non-compartmental PK analyses, including proper data formatting.

  • Support the development of Statistical Analysis Plans (SAPs) related to PK data.

  • Collaborate with cross-functional teams such as PBS and FSP within Cytel.

  • Participate in client meetings and communications as needed.

  • Contribute to clinical reports and slide decks presenting analysis results.

  • Ensure all work aligns with standard operating procedures (SOPs) and regulatory requirements.

  • Archive all data and results in accordance with internal documentation practices.


Work Locations

  • Ahmedabad, Gujarat, India

  • Pune, Maharashtra, India

  • Bharatpur, Rajasthan, 321001, India

  • Remote options available