Cytel Hiring Scientist Quantitative Pharmacologyist

Scientist QPP Vacancy in Hyderabad – Cytel India

Cytel hiring Scientist QPP with M.Pharmacy qualification. 4–6 years PK/PD experience required. Location: Hyderabad, India.

Cytel Inc. is hiring experienced pharmacokinetics and pharmacometrics professionals for the role of Scientist, QPP in India. This opportunity is designed for M.Pharmacy graduates with strong expertise in PK/PD analysis, clinical trial data interpretation, and regulatory deliverables. The role offers hands-on exposure to advanced quantitative pharmacology projects supporting global drug development programs, making it an ideal career move for professionals aiming to grow in clinical research, pharmacometrics, and regulatory science.

Company Overview

Cytel Inc. is a globally respected quantitative sciences and clinical research organization supporting pharmaceutical, biotechnology, and medical device companies across the full drug development lifecycle. Known for its deep expertise in biostatistics, pharmacometrics, quantitative pharmacology, and clinical trial analytics, Cytel plays a critical role in optimizing study design, regulatory strategy, and evidence generation.

With a strong presence in India, Cytel delivers high-impact scientific solutions that directly influence regulatory approvals and patient outcomes. The organization is trusted by global regulators and sponsors for its scientific rigor, compliance-driven processes, and innovation in clinical data analysis. Cytel’s work environment emphasizes technical excellence, continuous learning, and long-term career development for life sciences professionals.

Job Role & Responsibilities

As a Scientist, QPP at Cytel, you will be responsible for executing and delivering pharmacokinetic and pharmacodynamic analyses for clinical trials. This role requires strong scientific judgment, hands-on technical skills, and the ability to collaborate with cross-functional teams to support regulatory submissions.

Key Responsibilities

• Read, interpret, and understand clinical study protocols, Cytel work request documents, and project requirements
• Prepare and review Pharmacokinetic Analysis Plans (PKAP) based on clinical protocols and study specifications
• Perform data management, data cleaning, and integration activities using Phoenix WinNonlin® software
• Conduct PK/PD analysis using Phoenix WinNonlin® version 8.1 or higher, aligned with study requirements
• Plan, execute, and deliver pharmacokinetic assignments with a focus on quality and timelines
• Develop Tables, Listings, and Figures (TLFs) and summary reports for regulatory submissions
• Perform quality control and quality assurance checks on PK deliverables as per client specifications
• Mentor team members and contribute to technical and strategic capability building within the organization
• Coordinate with client points of contact to resolve data queries, clarify specifications, and manage review cycles
• Collaborate with statisticians, SAS® programmers, and medical writers on pharmacokinetic projects
• Ensure compliance with GCP, 21 CFR Part 11, ISO 17799, and internal SOPs

This role is critical in supporting regulatory decision-making and advancing clinical development programs through robust quantitative analysis.

Eligibility / Qualifications

Educational Qualification

Candidates must hold a master’s degree in pharmacy or a closely related discipline.

Accepted Education Backgrounds:
M.Pharmacy (Pharmacology, Pharmaceutics, Pharmaceutical Technology), MSc Pharmacology, MSc Pharmaceutics, MSc Pharmaceutical Sciences, or equivalent postgraduate life sciences qualifications.

Experience Requirements

• 4 to 6 years of hands-on experience in PK/PD analysis and reporting for clinical trials
• Proven expertise in using Phoenix WinNonlin® software for pharmacokinetic modeling
• Strong understanding of biopharmaceutics, pharmacology, and clinical research concepts

Technical & Functional Skills

• Advanced proficiency in Phoenix WinNonlin® for workflow creation and execution
• Strong knowledge of PK/PD principles, drug discovery, and drug development
• Experience in medical and scientific writing for clinical and regulatory documents
• Working knowledge of GraphPad Prism, R Programming, and SAS® software
• Solid understanding of ICH-GCP guidelines and clinical trial methodologies
• Excellent written and verbal communication skills

Location & Salary

Job Location

• Hyderabad, Telangana
• Office location: Raheja Mindspace, 5th Floor, 3B Tower, Mindspace, Hyderabad – 500081

Application Process

Interested candidates can apply directly through the official Cytel careers portal using the link below:

👉 Apply Now: https://iblyjb.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/cytel/job/944

Frequently Asked Questions (FAQs)

Who is eligible for the Scientist QPP role at Cytel?

Candidates with an M.Pharmacy degree and 4–6 years of experience in PK/PD analysis using Phoenix WinNonlin® are eligible to apply.

Is experience with Phoenix WinNonlin® mandatory?

Yes. Hands-on experience with Phoenix WinNonlin® version 8.1 or higher is a core requirement for this role.

What type of projects will I work on?

You will work on global clinical trial projects involving pharmacokinetic and pharmacodynamic analysis, regulatory submissions, and quantitative pharmacology support.

Is this a full-time position?

Yes. This is a full-time, office-based role located in Hyderabad.

What is the career growth potential at Cytel?

Cytel offers strong growth opportunities into senior pharmacometrician, quantitative pharmacology lead, and regulatory science roles, supported by exposure to global sponsors and advanced clinical research programs.

Summary Table

Category	Details
Company	Cytel Inc.
Vacancies	Scientist Quantitative Pharmacologyist
Required Education	M.Pharmacy (Pharmacology, Pharmaceutics, Pharmaceutical Technology), MSc Pharmaceutical Sciences
Experience	4–6 Years in PK/PD Analysis

Tagged as: Pharma Jobs in Hyderabad