Drug Safety Specialist/ Clinical Safety Coordinator
A Medpace pharmacovigilance job opportunity has emerged for aspiring Clinical Safety Coordinators in Navi Mumbai, India. This full-time, office-based position focuses on managing and processing adverse events from various sources, including clinical trials and post-marketing surveillance. Interested candidates are encouraged to apply soon.
About the Company
Medpace is a full-service clinical contract research organization (CRO) providing phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. The organization is dedicated to accelerating the global development of safe and effective medical therapeutics through the advancement of clinical research. With headquarters in Cincinnati, Ohio, Medpace employs more than 6,500 people across 40+ countries, leveraging in-country regulatory and therapeutic expertise across all major therapeutic areas.
Job Details:
- Location: Navi Mumbai, India
- Department: Clinical Safety
- Reference Number: 11946
Medpace Pharmacovigilance Job Description
In this Medpace pharmacovigilance job, the Clinical Safety Coordinator will be responsible for handling and processing adverse events from all sources. This role involves determining the plan of action for incoming calls, collecting, processing, and tracking incoming adverse and serious adverse events, writing safety narratives, and reporting on various safety data. Additionally, the coordinator will collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Key Responsibilities
- Determine plan of action for incoming calls.
- Collect, process, and track incoming adverse and serious adverse events.
- Write safety narratives.
- Report on various safety data.
- Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Eligibility Criteria
- Bachelor’s degree in a healthcare-related field such as Nursing, Pharmacy, or Pharmacology.
- Clinical experience or Clinical Research, case processing, and post-marketing pharmacovigilance experience is preferred.
- Proficient English is required.
- Proficient knowledge of Microsoft® Office.
- Broad knowledge of medical terminology.
- Strong organizational and communication skills.
Documents Required
- Resume/CV
- Cover Letter
- Academic Certificates
- Experience Certificates
How to Apply for This Medpace Pharmacovigilance Job
Interested candidates should apply through the following link: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
Why Join Medpace?
Joining Medpace means becoming part of an innovative team that is committed to bringing cutting-edge therapies to market. The organization focuses on scientific excellence and improving patient outcomes through continuous learning and cross-functional collaboration. Employees work alongside physicians, scientists, and industry-leading experts, contributing to an interactive team environment that fosters decision-making, creative thinking, and mutual trust.
Conclusion
This Medpace pharmacovigilance job is an excellent opportunity for qualified candidates to join Medpace as a Clinical Safety Coordinator in Navi Mumbai. Interested individuals are encouraged to apply at the earliest to be considered for this impactful role in clinical safety.
