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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🏢 About Company
Clinztech is an organization operating in the clinical research and life sciences domain. The company focuses on supporting research activities, data processes, and clinical workflows in compliance with industry standards. Clinztech provides learning‑oriented roles that help professionals understand the practical aspects of clinical research while working in a structured and process‑driven environment.
📊 Role 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
📌 Available Positions & Key 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.
🎓 Qualification Required
- 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.
⭐ Role Insight
These roles offer exposure to real‑world clinical research operations. Working in such positions helps candidates understand how research data is generated, managed, and maintained throughout a study lifecycle. This experience is valuable for building a long‑term career in clinical research, pharmacovigilance, regulatory affairs, or related healthcare domains.
🎯 Ideal Candidates
- Fresh graduates in Life Sciences or Pharmacy
- Candidates seeking entry into clinical research
- Professionals looking to switch into the life sciences domain
- Individuals interested in research‑oriented careers
💰Expected Salary
- Entry‑Level Roles: ₹2.5 – ₹4.5 LPA
- Salary depends on role complexity, experience, and company policy.
💡 Expert Tips
- Revise basic clinical research and GCP concepts
- Understand the importance of data accuracy
- Highlight life science knowledge in your resume
- Be ready to explain your interest in clinical research
🔗 Application Details
Interested candidates can send their updated CV to the email ID below:
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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❓ Frequently Asked Questions -Multiple Positions in Clinical Research & Life Sciences
1. Who can apply for these roles at CLINZTECH?
Anyone with a Bachelor’s or Master’s degree in Life Sciences such as B.Pharm, M.Pharm, B.Sc, or M.Sc can apply.
2. Are these roles suitable for freshers?
These roles are perfect for freshers. Candidates with 0–2 years of experience are also welcome.
3. What positions are currently open?
Clinical Data Analyst I
SAS Programmer I
Biostatistician I
Pharmacovigilance Associate I
4. Do I need prior work experience?
No. Prior experience is not mandatory.
Basic knowledge and interest in clinical research is enough. Training will be provided
5. Will CLINZTECH provide training?
CLINZTECH offers on‑the‑job training and mentoring to help freshers learn tools, processes, and industry standards.
