Medpace Clinical Safety Coordinator job 2026. Check eligibility, nursing requirements, pharmacovigilance role details, and apply online for clinical safety career opportunity.
Introduction
Are you from a nursing or life sciences background and looking to build a career in pharmacovigilance and clinical safety? The Clinical Safety Coordinator job at Medpace is an excellent opportunity to work in a global CRO environment. This role focuses on adverse event processing, safety data management, and clinical research compliance, making it ideal for candidates aiming to grow in drug safety and clinical research domains.
Job Overview
| Details | Information |
|---|---|
| Job Title | Clinical Safety Coordinator |
| Company Name | Medpace |
| Location | India (Office-Based) |
| Employment Type | Full-Time, Permanent |
| Department | Clinical Safety / Pharmacovigilance |
| Experience Required | Clinical / Healthcare Background Preferred |
| Education | B.Sc Nursing / MSc Nursing |
| Salary | As per company standards |
Company Overview
Medpace is a globally recognized Contract Research Organization (CRO) headquartered in the United States. The company provides Phase I–IV clinical development services to pharmaceutical, biotechnology, and medical device companies. With operations in over 40 countries, Medpace is known for its scientific expertise, high-quality standards, and contribution to developing safe and effective therapies worldwide.
Job Location & Employment Type
- Location: India (Office-Based Role)
- Employment Type: Full-Time, Permanent
- Industry: Pharmaceutical & Life Sciences / Clinical Research
Open Positions / Department Details
The role is part of the Clinical Safety / Pharmacovigilance Department, focusing on adverse event management and safety data reporting across clinical trials and post-marketing surveillance.
Key Roles & Responsibilities
As a Clinical Safety Coordinator, your responsibilities will include:
- Manage incoming safety-related communications and determine appropriate actions
- Collect, process, and track adverse events (AEs) and serious adverse events (SAEs)
- Prepare detailed safety narratives for reported cases
- Analyze and report safety data accurately
- Collaborate with internal teams and clinical research sites
- Ensure compliance with global safety and regulatory guidelines
- Maintain proper documentation and data tracking systems
Eligibility Criteria
Education
- Bachelor of Science in Nursing (B.Sc Nursing)
- Master’s Degree in Nursing (M.Sc Nursing – Preferred)
- B.Sc / M.Sc in Life Sciences (as per role flexibility)
Experience
- Clinical experience in hospital or healthcare settings preferred
- Freshers with strong medical knowledge may be considered
Skills Required
- Strong understanding of medical terminology
- Knowledge of pharmacovigilance and safety reporting (preferred)
- Proficiency in Microsoft Office tools
- Good communication and organizational skills
- Attention to detail and documentation accuracy
Salary & Benefits
- Salary: As per company standards
- Flexible work environment
- Competitive compensation and benefits
- Paid time off (PTO)
- Structured career growth paths
- Employee wellness programs
- Company-sponsored events and recognition programs
Selection Process
The hiring process generally includes:
- Resume Screening
- Technical/Domain Interview
- HR Interview
- Final Selection
How to Apply
Interested candidates should apply through the official online application portal of the company. Shortlisted candidates will be contacted by the Medpace recruitment team for further steps.
Important Dates
- Apply as early as possible
- Shortlisting will be done on a rolling basis
Why Apply for This Job?
The Clinical Safety Coordinator job at Medpace offers a strong entry into pharmacovigilance and clinical research careers.
- Work with a global CRO organization
- Gain hands-on experience in adverse event processing
- Exposure to clinical trials and safety reporting systems
- Opportunity to grow in pharmacovigilance and regulatory roles
- Contribute to improving patient safety worldwide
FAQs
1. Who can apply for this Clinical Safety Coordinator job?
Candidates with B.Sc Nursing, M.Sc Nursing, or Life Sciences background can apply.
2. Is clinical experience mandatory?
Clinical experience is preferred but not always mandatory for strong candidates.
3. What is the job role about?
The role involves adverse event processing, safety reporting, and clinical data handling.
4. What skills are required?
Medical terminology knowledge, communication skills, and attention to detail are essential.
5. How can I apply for this job?
You can apply through the company’s official online application portal.
Conclusion
If you are looking to enter the field of pharmacovigilance and clinical safety, this opportunity at Medpace is highly valuable. With global exposure, structured career growth, and meaningful work in patient safety, this role can be a strong foundation for your future in clinical research. Apply now and take the next step in your career.
Disclaimer
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