Pfizer hiring Central Monitoring Specialists in Chennai for freshers and experienced candidates with SAS and clinical research skills needed
Introduction
The pharmaceutical and clinical research industry continues to expand rapidly, creating strong demand for skilled professionals in data-driven roles. One such promising opportunity is now open with Pfizer for Central Monitoring Specialist positions in Chennai. This role is ideal for candidates looking to build expertise in clinical data analysis, risk-based monitoring, and SAS programming. Whether you are a fresher with relevant training or an experienced professional, this opening offers a solid career pathway in clinical research.
Company Overview
Pfizer is one of the world’s leading pharmaceutical organizations, known for its innovation in medicines, vaccines, and clinical research. With a strong global presence, Pfizer focuses on improving patient outcomes through advanced research and data-driven healthcare solutions. The company provides excellent career opportunities, especially in areas such as clinical trials, pharmacovigilance, and data analytics.
Job Overview
| Job Title | Central Monitoring Specialist (Associate / Senior Associate) |
|---|---|
| Company Name | Pfizer |
| Location | Chennai, Tamil Nadu |
| Employment Type | Full-Time |
| Qualification | B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences |
| Experience | 0 – 5 Years |
| Salary | As per company norms |
| Application Mode | Email Application |
Job Location & Employment Type
This position is based in Chennai, Tamil Nadu, with a hybrid working model. Candidates may be required to work both remotely and from the office depending on project needs. It is a full-time role offering long-term career stability and growth.
Open Positions / Department Details
Pfizer is hiring for Central Monitoring Specialist roles under clinical research and data monitoring departments. The positions are available at Associate and Senior Associate levels depending on the candidate’s experience and expertise.
The hiring focuses on professionals interested in:
- Centralized Monitoring
- Risk-Based Monitoring (RBM)
- Clinical Data Analysis
- SAS Programming
Key Roles & Responsibilities
Candidates selected for this role will be responsible for a wide range of clinical data monitoring and analytical tasks. Major responsibilities include:
- Conduct centralized monitoring of clinical trial data using structured RBM methodologies
- Perform risk assessment using Key Risk Indicators (KRIs) and identify potential issues in clinical studies
- Analyze clinical datasets using SAS programming tools and techniques
- Assist in the setup, configuration, and maintenance of RBM systems
- Work closely with cross-functional teams such as Clinical Data Management, Biostatistics, and Clinical Operations
- Ensure compliance with international guidelines such as ICH-GCP and regulatory requirements
- Detect data inconsistencies, trends, and anomalies within clinical trial datasets
- Prepare detailed reports, dashboards, and insights for informed decision-making
- Support continuous improvement initiatives in centralized monitoring processes
- Maintain documentation and ensure accuracy of data analysis outputs
Eligibility Criteria
Education:
Candidates must have completed any of the following qualifications:
- B.Pharm
- M.Pharm
- Pharm.D
- BSc or MSc in Life Sciences or related fields
Experience:
- Freshers with relevant internships or training can apply
- Candidates with up to 5 years of experience in clinical research or data analytics are eligible
Skills Required:
Technical Skills:
- Strong knowledge of SAS programming (mandatory requirement)
- Understanding of clinical trial processes and protocols
- Familiarity with ICH-GCP guidelines
- Knowledge of RBM frameworks and centralized monitoring concepts
- Basic understanding of SQL, PL-SQL, or Oracle Clinical (preferred)
- Exposure to Electronic Data Capture (EDC) systems
Soft Skills:
- Analytical thinking and problem-solving ability
- Strong communication and interpersonal skills
- Attention to detail and data accuracy
- Ability to work in cross-functional teams
- Time management and multitasking capability
Salary & Benefits
- Salary: As per company norms
- Opportunity to work with a globally recognized pharmaceutical leader
- Exposure to advanced clinical research methodologies and technologies
- Hybrid work flexibility for better work-life balance
- Strong learning environment for developing SAS and data analytics skills
- Career progression opportunities in clinical data management and monitoring
Selection Process
The selection process for this role typically involves multiple stages to evaluate both technical and communication skills:
- Initial application screening
- Technical interview focusing on SAS, clinical trials, and RBM concepts
- Functional or managerial interview
- HR discussion and final selection
Candidates should be well-prepared with clinical research fundamentals and programming knowledge to succeed in the selection process.
How to Apply
Interested candidates can apply through the official application method provided below:
- Email your updated resume to: sabita.roy@pfizer.com
Ensure that your resume clearly highlights your SAS skills, clinical research knowledge, and any relevant internship or project experience.
Why Apply for This Pharma Job?
This opportunity at Pfizer offers more than just employment—it provides a platform to build a strong career in one of the fastest-growing domains of the pharmaceutical industry. Central monitoring and risk-based monitoring are becoming essential in modern clinical trials, making this role highly future-oriented.
Candidates will gain hands-on experience in real-world clinical data analysis, learn advanced monitoring techniques, and work with global teams. The exposure to SAS programming and RBM frameworks significantly enhances career prospects in clinical research, data science, and pharmacovigilance.
Additionally, working with a reputed company like Pfizer adds strong value to your professional profile and opens doors to global opportunities.
Important Note / Disclaimer
PharmaJobHub.in is an independent job information platform. We do not provide any recruitment guarantee and are not affiliated with any company. Candidates are advised to verify details from official sources before applying.
Final Call-to-Action
Candidates interested in building a career in clinical data analytics and centralized monitoring are encouraged to apply at the earliest. Early applications increase your chances of selection, especially for competitive roles in leading pharmaceutical companies like Pfizer.
