Biomapas Pharmacovigilance Jobs - 2026 | Remote PV Specialist (Case Processing) Hiring (Biomapas Pharmacovigilance Jobs - 2026) Introduction If you are looking to start or grow your career in pharmacovigilance and drug safety, this is an excellent opportunity. Biomapas (Delta PV division) is hiring Pharmacovigilance Specialists for remote roles. With the increasing demand for drug safety professionals worldwide, this role offers strong exposure to ICSR case processing, regulatory compliance, and global pharmacovigilance operations. Whether you are a fresher or have some PV experience, this opportunity can help you build a solid career in clinical research and drug safety. Looking for the best multivitamin? Here is the top recommendation: 👉 HealthKart Multivitamin – Best for Daily Energy 👉 Buy Now on Amazon (Best Price) About The Company Biomapas is a globally recognized Contract Research Organization (CRO) specializing in pharmacovigilance, regulatory affairs, and clinical r...
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"Clinical Research Associate (CRA) Job in New Delhi – The George Institute Hiring | Apply Now 2026"
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Clinical Research Associate (CRA) Job in New Delhi – The George Institute Hiring 2026
(Clinical Research Associate (CRA) Job in New Delhi)
If you are looking for a Clinical Research Associate (CRA) job in Delhi with an internationally recognised medical research organisation, this opportunity can be a major career breakthrough. The George Institute is hiring an experienced Clinical Research Associate for its New Delhi operations to manage multi-site global clinical trials focused on non-communicable diseases (NCDs).
This pharma job opening is ideal for professionals with at least 2 years of clinical trial coordination experience who want to grow in global clinical research, regulatory compliance, and ICH-GCP-based trial monitoring.
Introduction
Clinical Research Associate (CRA) roles are among the most respected and growth-oriented positions in the clinical research and pharmaceutical industry. With increasing global focus on cardiovascular, renal, and chronic disease research, experienced CRAs are in high demand.
The George Institute’s CRA job in New Delhi offers exposure to international clinical trials, regulatory coordination, site monitoring, and ethics committee submissions. This role is suitable for life science and medical professionals who want to work in structured, compliance-driven research environments.
About The Company
The George Institute for Global Health is a globally recognised independent medical research organisation founded in 1999. The institute is headquartered in Sydney, Australia, and operates in more than 40 countries worldwide.
It has over 700 researchers and staff members working across multiple global research centres. The organisation focuses on improving health outcomes in non-communicable diseases (NCDs), including cardiovascular diseases, kidney disorders, diabetes, and chronic conditions.
The institute collaborates with leading universities and healthcare systems globally and is known for maintaining high ethical research standards, regulatory compliance, and impact-driven global clinical research programs.
Job Overview Summary
The Clinical Research Associate (CRA) position is an intermediate-level clinical research role based in New Delhi. The selected candidate will be responsible for managing clinical trial operations across multiple sites, ensuring compliance with ICH-GCP guidelines, coordinating regulatory approvals, and performing site monitoring activities.
This is a two-year contract position (extendable) and reports to the Senior Project Manager. The role involves significant coordination with investigators, ethics committees, and regulatory authorities.
Vacancy Details (Official)
Job Title: Clinical Research Associate (CRA) Location: New Delhi Employment Type: Two-year contract (extendable) Department: Projects Career Level: Intermediate Reporting To: Senior Project Manager
Responsibility Explanation
As a Clinical Research Associate, you will handle complete clinical trial management activities, including study start-up, monitoring, documentation, and site close-out processes.
Clinical Trial Start-Up
You will assist in preparing essential trial documents such as the study protocol, Investigator’s Brochure, Case Report Forms (CRF), and patient information sheets. You will coordinate with Ethics Committees and regulatory bodies to obtain necessary approvals.
Site Monitoring & Execution
You will conduct on-site monitoring visits and perform Source Data Verification (SDV) to ensure trial data accuracy. Training site staff on study-specific procedures and ensuring compliance with ICH-GCP standards will be a key responsibility.
Documentation & Close-Out
The role includes preparing monitoring reports, maintaining trial master files, archiving documents, and closing study sites after completion. Regulatory documentation accuracy and compliance will be critical.
Eligibility (Official)
Candidates must have:
Qualification in Life Sciences, Medical Sciences, or Nursing
Minimum 2 years of clinical trial coordination experience
Strong knowledge of ICH-GCP guidelines
Experience in Ethics Committee submissions
Experience in Regulatory approvals
Knowledge of Clinical documentation and CRF handling
Willingness to travel for site monitoring visits
Excellent English communication skills
Skills Required
To succeed in this Clinical Research Associate job, candidates should have:
Strong understanding of clinical operations
Regulatory compliance knowledge
Good documentation and reporting skills
Site coordination and stakeholder management abilities
Risk identification and problem-solving skills
Ability to manage multi-site clinical trials
Attention to detail and data accuracy
Professional communication skills
Experience in cardiovascular research, renal trials, or NCD-focused clinical studies will be an added advantage.
Salary Estimate
Based on similar Clinical Research Associate jobs in Delhi, the estimated salary range is:
₹5,00,000 – ₹8,50,000 per annum
Salary may vary depending on experience, previous trial exposure, and negotiation during the interview process.
Interview Details (Official)
Shortlisted candidates will be contacted by the HR team. The selection process may include:
Initial HR screening
Technical interview
Project management discussion
Final approval by the department head
Required Documents
Candidates should keep the following documents ready:
Minimum 2 years of clinical trial coordination experience is required.
Q2. Is this a permanent job?
It is a two-year contract role, which may be extended based on performance.
Q3. Is travel required?
Yes, site monitoring visits require travel.
Q4. What disease areas are involved?
The role focuses mainly on non-communicable diseases such as cardiovascular and renal disorders.
Q5. Is ICH-GCP knowledge mandatory?
Yes, a strong understanding of ICH-GCP guidelines is essential.
Final Conclusion
The Clinical Research Associate job at The George Institute in New Delhi is an excellent opportunity for professionals seeking growth in global clinical research operations. With exposure to international trials, regulatory coordination, and multi-site study management, this role can significantly strengthen your CRA career profile.
If you meet the eligibility criteria and have hands-on clinical trial experience, applying for this pharma job in Delhi can be a strong career move in 2026.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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