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37 Medpace Clinical Research India Jobs

Drug Safety Specialist / Clinical Safety Coordinator

2-4 years

Navi Mumbai

1 vacancy

Drug Safety Specialist / Clinical Safety Coordinator

Medpace Clinical Research India

posted 2hr ago

Job Role Insights

Flexible timing

Job Description

 Job Summary

We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance.

If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you!

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; and
Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.


Qualifications

Bachelor's degree in Healthcare related field; Nursing, Pharmacy, Pharmacology, etc
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; and
Strong organizational and communication skills.


Employment Type: Full Time, Permanent

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Drug Safety Specialist salary at Medpace Clinical Research India

reported by 1 employee
₹3.8 L/yr - ₹4.9 L/yr
28% less than the average Drug Safety Specialist Salary in India
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What Medpace Clinical Research India employees are saying about work life

based on 8 employees
100%
100%
42%
Flexible timing
Monday to Friday
No travel
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Medpace Clinical Research India Benefits

Team Outings
International Relocation
Job Training
Gymnasium
Cafeteria
Work From Home +6 more
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