Clinztech Hiring – Multiple Positions in Clinical Research & Life Sciences | Hyderabad

Clinztech, a growing organization in the clinical research and life sciences domain, is hiring for multiple roles at its Hyderabad location. These opportunities are suitable for fresh graduates holding a Bachelor’s or Master’s degree in Life Sciences who are looking to start their careers in clinical research, life sciences operations, and healthcare domains.

Clinztech offers entry‑level roles across various functions, providing hands‑on exposure to clinical research processes, documentation, data handling, and regulatory‑aligned workflows. Candidates will work in a structured, learning‑focused environment that supports skill development and early career growth.

This is an excellent opportunity for Life Sciences freshers aiming to build a strong foundation and grow within the clinical research and healthcare industry.

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Job Overview

• Position:
  • Clinical Data Analyst I
  • SAS Programmer I
  • Biostatistician I
  • Pharmacovigilance Associate I
• Department: CDM & PV
• Location: Hyderabad
• Experience: 0 to 2 years
• Qualification: B.Pharm, M.Pharm,Lifesciences
• Job Type: Full-Time
• Last date of application :Not provided

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Available Roles & Responsibilities

1.Clinical Data Analyst I

• Analyze and interpret clinical trial data to identify trends, patterns, and insights that support study objectives.
• Develop, update, and maintain databases and data tracking systems used for managing clinical trial data.
• Collaborate with clinical research, biostatistics, programming, and operations teams to ensure timely delivery of accurate and high‑quality data outputs.
• Perform quality control (QC) checks on data entry, validation, and analysis to ensure accuracy, consistency, and compliance with study requirements.
• Provide technical support and guidance to junior team members on data analysis tools, processes, and best practices.

2. SAS Programmer I

• Support planning, execution, and management of SAS programming activities for clinical research projects.
• Develop, validate, and maintain SAS programs to support data analysis, reporting, and project deliverables.
• Work closely with biostatistics, clinical data management, and project teams to meet study objectives and timelines.

3. Biostatistician I

• Develop and apply statistical models and analytical methods to analyze complex biological and clinical research data.
• Collaborate with cross‑functional teams (clinical research, data management, SAS programming) to support study design and execution.
• Analyze and interpret large datasets to identify trends, patterns, and meaningful insights that support research objectives.
• Design and document statistical analysis plans, protocols, and procedures for assigned research projects.

4.Pharmacovigilance Associate I

• Perform thorough reviews of clinical trial and safety data to identify potential safety concerns and emerging risks.
• Support the development and implementation of pharmacovigilance strategies to effectively monitor and mitigate product safety risks.
• Collaborate with cross‑functional teams to ensure compliance with global pharmacovigilance regulations, guidelines, and SOPs.
• Analyze complex safety datasets to identify trends, patterns, and signals that may impact product benefit‑risk profiles.
• Prepare safety reports, summaries, and presentations to clearly communicate findings to internal teams and stakeholders.

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Required Skills & Qualifications

• Bachelor’s or Master’s degree in Life Sciences or a related discipline, including B.Pharm, M.Pharm
• 0–2 years of experience is suitable for all listed roles.
• Fresh graduates with strong academic foundations and interest in clinical research are encouraged to apply.
• Basic understanding of clinical research processes, clinical trials, and healthcare or life sciences concepts.
• Awareness of regulatory, data quality, or safety principles relevant to the role applied for is an advantage.
• Proficiency in Microsoft Office applications (Word, Excel, PowerPoint) for documentation, data handling, and reporting.
• Willingness to learn role‑specific tools such as EDC systems, statistical software, SAS, or safety databases, depending on assigned position.
• Strong analytical thinking with attention to detail.
• Ability to interpret data, identify issues, and contribute to quality‑focused outcomes.
• Good written and verbal communication skills.
• Ability to work effectively in cross‑functional and team‑based environments.
• Strong organizational and time‑management skills.
• Willingness to learn, take ownership of tasks, and adapt in a fast‑paced clinical research environment.
• Commitment to following SOPs, quality standards, and regulatory guidelines applicable to clinical research and life sciences operations.

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Why Join CLINZTECH?

• When you join CLINZTECH, you become part of a team that works to bring new medicines and healthcare solutions to patients faster. The company works on real projects that matter, using the latest science and technology to improve people’s lives across the world.
• At CLINZTECH, there is a strong focus on learning, teamwork, and personal growth. Every employee is encouraged to share ideas, learn new skills, and grow in their career. Your work is valued, your development is supported, and you become part of a bigger mission to improve global health.

How to Apply

Interested candidates can send their updated CV to the email ID below:

📧careers@clinztech.com

Use a clear subject line like: “Application for [ROLE]- [Your Name]”

Always attach your updated resume in PDF format

Note: Only shortlisted candidates will be contacted for further steps.

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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