Medpace Clinical Research India is hiring for two positions in Navi Mumbai: Randomization & Study Product Coordinator and Drug Safety Specialist/Clinical Safety Coordinator. The openings are suitable for candidates with backgrounds in life sciences, healthcare, pharmacy, pharmacology, clinical research, and pharmacovigilance.
Job Details
| Particular | Details |
|---|---|
| Company | Medpace Clinical Research India |
| Location | Navi Mumbai |
| Industry | Pharmaceutical & Life Sciences |
| Employment Type | Full Time, Permanent |
| Work Mode | Office-based |
| Positions | Randomization & Study Product Coordinator; Drug Safety Specialist/Clinical Safety Coordinator |
1. Randomization & Study Product Coordinator
Experience: 0โ2 years
Location: Navi Mumbai
Level: Entry Level
The Randomization & Study Product Coordinator will work with the RSPM team to support the accuracy of RSPM system data and assist with study product management for clinical studies.
Responsibilities
- Provide general Randomization & Study Product Management support.
- Support study product management.
- Assist the Project Manager with system design and setup.
- Work with clients to obtain requirements and respond to inquiries.
- Create study-specific documents.
- Maintain study documentation.
- Perform other assigned projects and tasks.
Eligibility & Qualifications
- Bachelor’s degree in Life Sciences or a related field.
- Basic knowledge of clinical research methodologies.
- Advanced working knowledge of Microsoft Excel.
- Strong attention to detail.
This is an entry-level position with an extensive onboarding and training process for new hires.
2. Drug Safety Specialist / Clinical Safety Coordinator
Experience: 1โ3 years
Location: Navi Mumbai
The Clinical Safety Coordinator will work within the Clinical Safety department, handling and processing adverse events from clinical trials and post-marketing surveillance sources.
Responsibilities
- Determine the appropriate plan of action for incoming calls.
- Collect, process, and track incoming adverse events and serious adverse events.
- Write safety narratives.
- Report on safety data.
- Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Eligibility & Qualifications
- Bachelor’s degree in a healthcare-related field, including:
- Nursing
- Pharmacy
- Pharmacology
- Clinical experience, clinical research, case processing, or post-marketing pharmacovigilance experience is preferred.
- Proficient English.
- Proficient knowledge of Microsoft Office.
- Broad knowledge of medical terminology.
- Strong organizational and communication skills.
Skills Required
Candidates applying for these Medpace Clinical Research India jobs may benefit from skills and knowledge in:
- Clinical Research
- Clinical Trials
- Pharmacovigilance
- Drug Safety
- Case Processing
- Pharmacology
- Clinical Development
- Medical Terminology
- Safety Data
- Microsoft Office
- Microsoft Excel
- Scientific Writing
- Communication
- Documentation
- Requirement Gathering
About Medpace Clinical Research India
Medpace is a full-service clinical contract research organization (CRO) providing Phase IโIV clinical development services to the biotechnology, pharmaceutical, and medical device industries. The company works across therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective areas.
Medpace is headquartered in Cincinnati, Ohio, and employs more than 6,500 people across 40+ countries.
Work Environment & Benefits
Medpace highlights the following employee offerings and development opportunities:
- Office-based environment with on-site mentors.
- Defined career paths and advancement opportunities.
- Industry-focused onboarding and training programs.
- Ongoing training and continuous learning.
- Competitive compensation programs.
- Health, wellness, retirement, and PTO benefits.
- Occasional work-from-home flexibility for eligible positions after training.
- Company-sponsored social events.
Benefits may vary by country.