Medpace, a globally recognized Clinical Research Organization (CRO), is seeking a dedicated Drug Safety Specialist/Clinical Safety Coordinator. This full-time, office-based role is located in our Navi Mumbai, India office. It offers an exciting opportunity to join our esteemed Clinical Safety department.
You will play a crucial role in handling and processing adverse events from various sources. This includes clinical trials and post-marketing surveillance. If you’re ready to advance your career in a dynamic environment, this is the perfect opportunity for you.
Contents
About Medpace: A Global Leader in Clinical Development
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
Our mission is to accelerate the global development of safe and effective medical therapeutics. We achieve this through a scientific and disciplined approach. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across more than 40 countries.
Our Commitment to Scientific Excellence
We leverage local regulatory and therapeutic expertise across all major areas. This includes oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective.
Our unwavering commitment to quality and ethical standards has made us a trusted partner for our sponsors. We are dedicated to making a difference in the lives of patients worldwide.
The Role: Drug Safety Specialist/Clinical Safety Coordinator
This position is integral to our Clinical Safety department. The successful candidate will be responsible for a variety of tasks related to pharmacovigilance and drug safety. This ensures the highest standards of patient safety are maintained throughout the clinical trial process.
Key Responsibilities:
| Responsibility | Description |
| Incoming Call Management | Determine the appropriate plan of action for incoming calls related to adverse events. |
| Adverse Event Processing | Collect, process, and track incoming adverse and serious adverse events. |
| Safety Narratives | Write clear and concise safety narratives for regulatory submissions. |
| Data Reporting | Report on various safety data to internal and external stakeholders. |
| Collaboration | Work closely with internal departments and clinical research sites to ensure compliance with safety processes. |
Who We’re Looking For:
We are seeking a candidate with a strong background in healthcare and a passion for clinical research. The ideal candidate will possess the following qualifications:
- Educational Background: A Bachelor’s degree in a healthcare-related field is required. This includes Nursing, Pharmacy, Pharmacology, or a related discipline.
- Experience: Previous experience in a clinical setting or clinical research is highly preferred. Experience in case processing and post-marketing pharmacovigilance is also a significant advantage.
Skills:
- Proficient in English (both written and verbal).
- Excellent knowledge of Microsoft® Office.
- A broad understanding of medical terminology.
- Strong organizational and communication skills.
How to Apply
If you are interested in the job role, click on the button below to apply and submit your resume. The MedPace Team will review your resume and email you back if you are selected. It may take 10-15 working days.
Verified Clinical Research Job Post
The post is released by the Medpace Official Career Webpage. Click here to visit the post
Why Medpace? People. Purpose. Passion.
At Medpace, we believe in the power of our people. We are driven by a shared purpose to make a difference in the world. Our passion for our work has a positive impact on the lives of countless patients and families.
Medpace Perks:
- Flexible Work Environment: We offer a flexible work environment that promotes work-life balance.
- Competitive Compensation: We provide a competitive compensation and benefits package.
- Generous PTO: Our competitive PTO packages allow for ample time off.
- Career Growth: We offer structured career paths with opportunities for professional growth.
- Employee Appreciation: We host company-sponsored employee appreciation events.
- Health and Wellness: We have various employee health and wellness initiatives.
Join Our Award-Winning Team
Medpace has been recognized by Forbes as one of America’s Most Successful Midsize Companies for four consecutive years (2021-2024). We have also received CRO Leadership Awards from Life Science Leader magazine. These awards are a testament to our expertise, quality, and reliability.
If you are ready to make a difference tomorrow, join us today.
Explore these Related Pharma Jobs:
Telegram
LinkedIn
Instagram
WhatsApp