Apply for Medpace Hiring Drug Safety Specialist / Clinical Safety Coordinator in Navi Mumbai and reporting expertise.
Introduction
Medpace has announced a promising career opportunity for the position of Drug Safety Specialist / Clinical Safety Coordinator in Navi Mumbai, India. This role is ideal for pharmacy, nursing, pharmacology, and healthcare professionals looking to build a successful career in pharmacovigilance and clinical safety. The position focuses on adverse event processing, safety case management, safety reporting, and regulatory compliance. Candidates searching for Pharma Jobs 2026, Pharmacovigilance Jobs, Clinical Research Jobs, Regulatory Affairs Jobs, and Drug Safety careers should consider this excellent opportunity with Medpace, one of the world’s leading Contract Research Organizations (CROs).
About Company
Medpace is a global full-service Contract Research Organization (CRO) dedicated to accelerating the development of safe and effective medical therapies. Founded more than three decades ago and headquartered in Cincinnati, Ohio, USA, Medpace provides comprehensive Phase I-IV clinical development services to pharmaceutical, biotechnology, and medical device companies worldwide.
The company operates in over 40 countries with a workforce of more than 6,000 professionals. Medpace supports clinical development across numerous therapeutic areas, including oncology, cardiology, endocrinology, metabolic diseases, central nervous system disorders, anti-infective therapies, and antiviral treatments. Through its scientific expertise, operational excellence, and commitment to quality, Medpace continues to be a trusted partner in advancing innovative healthcare solutions globally.
Recognized multiple times by Forbes and industry-leading organizations, Medpace remains one of the most respected names in clinical research and drug development.
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Job Details / Job Summary
| Particulars | Details |
|---|---|
| Company Name | Medpace |
| Job Role | Drug Safety Specialist / Clinical Safety Coordinator |
| Department | Clinical Safety |
| Qualification Required | B.Pharm, M.Pharm, Pharm.D, Nursing, Pharmacology, Life Sciences, Healthcare Related Degree |
| Experience Required | Freshers and Experienced Candidates May Apply |
| Salary Package | ₹4.5 LPA – ₹9 LPA (Expected) |
| Job Location | Navi Mumbai, Maharashtra |
| Employment Type | Full-Time |
| Industry Type | Clinical Research Organization (CRO) |
| Shift Timing | As Per Business Requirements |
| Gender Eligibility | Male & Female |
| Application Mode | Online Application |
| Selection Process | Resume Screening, Technical Interview, HR Interview |
| Skills Required | Adverse Event Processing, Case Handling, Pharmacovigilance, Safety Reporting, Medical Terminology |
| Official Notification Status | Active |
| Application Last Date | Apply As Soon As Possible |
Eligibility Criteria
Candidates interested in this Pharma Company Hiring opportunity should meet the following requirements:
- Bachelor’s degree in Pharmacy, Nursing, Pharmacology, Life Sciences, or related healthcare discipline.
- Clinical experience, clinical research experience, or post-marketing pharmacovigilance experience is preferred.
- Understanding of adverse event reporting and drug safety processes.
- Good command of English communication, both written and spoken.
- Proficiency in Microsoft Office applications.
- Knowledge of medical terminology and healthcare concepts.
- Strong organizational and documentation skills.
- Ability to work effectively in a team environment.
Required Skills
The ideal candidate should possess the following professional skills:
- Pharmacovigilance case processing
- Adverse event management
- Serious adverse event reporting
- Safety narrative writing
- Clinical safety operations
- Medical terminology knowledge
- Regulatory compliance awareness
- Data tracking and reporting
- Documentation management
- Communication and coordination skills
- Clinical research understanding
- Time management and multitasking abilities
- Microsoft Office proficiency
Roles and Responsibilities
The selected candidate will be responsible for supporting clinical safety and pharmacovigilance activities.
Key responsibilities include:
- Evaluate and determine appropriate actions for incoming safety-related communications.
- Collect, review, process, and track adverse event reports.
- Handle serious adverse event (SAE) case documentation and follow-up activities.
- Prepare accurate and compliant safety narratives.
- Generate and maintain various safety-related reports.
- Support pharmacovigilance case processing activities.
- Collaborate with clinical research sites and internal teams.
- Ensure compliance with established safety procedures and regulations.
- Maintain high-quality documentation and case records.
- Assist in managing safety information from clinical trials and post-marketing sources.
- Support ongoing clinical safety operations and reporting activities.
- Contribute to process improvements within the clinical safety department.
Salary Details
Medpace offers attractive salary packages based on educational qualifications, professional experience, and technical competencies.
Expected Salary Range
| Experience Level | Expected Annual Salary |
|---|---|
| Freshers | ₹4.5 LPA – ₹6 LPA |
| 1–3 Years Experience | ₹6 LPA – ₹9 LPA |
| Experienced Safety Professionals | ₹9 LPA+ |
Additional benefits may include:
- Flexible work environment
- Competitive compensation package
- Paid leave benefits
- Career development programs
- Employee wellness initiatives
- Performance recognition programs
- Global exposure opportunities
Selection Process
The recruitment process generally includes the following stages:
Step 1: Online Application
Candidates must submit their updated resumes through the official Medpace careers portal.
Step 2: Resume Screening
The recruitment team reviews educational qualifications, experience, and relevant skills.
Step 3: Technical Evaluation
Shortlisted applicants may undergo an assessment related to pharmacovigilance, clinical safety, and adverse event processing.
Step 4: Interview Round
Candidates participate in technical and HR interviews.
Step 5: Final Selection
Successful candidates receive an official offer letter and onboarding instructions.
How to Apply
Interested candidates can apply online by following these steps:
- Visit the official Medpace careers website.
- Search for the position “Drug Safety Specialist / Clinical Safety Coordinator.”
- Read the complete job description and eligibility criteria.
- Update your resume with relevant educational qualifications and experience.
- Complete the online application form.
- Submit your application before the position is filled.
- Monitor your email for recruitment updates.
Candidates searching for B.Pharm Jobs, M.Pharm Jobs, Pharmacovigilance Jobs, Clinical Research Jobs, Regulatory Affairs Jobs, Freshers Pharma Jobs, and Latest Pharma Jobs should apply as soon as possible.
Frequently Asked Questions
1. What qualifications are required for the Drug Safety Specialist role?
Candidates with B.Pharm, M.Pharm, Pharm.D, Nursing, Pharmacology, Life Sciences, or related healthcare qualifications are eligible to apply.
2. Can freshers apply for this position?
Yes. Freshers with relevant healthcare or life sciences qualifications may be considered. Previous clinical research or pharmacovigilance exposure will be an added advantage.
3. What salary can candidates expect?
The expected salary typically ranges between ₹4.5 LPA and ₹9 LPA depending on qualifications, skills, and experience.
4. How can I apply for this Medpace job?
Candidates can apply online through the official Medpace careers portal after reviewing the eligibility criteria and job requirements.