Job title: Drug Safety Specialist
Location: Navi Mumbai, India
Job Category: Clinical Safety
Req ID: 10022
About the Job:
We are looking for a Clinical Safety Coordinator to join our team. This is a full-time, office-based job in our Clinical Safety department. As a Clinical Safety Coordinator, you will play a crucial role in ensuring the safety of patients by handling and processing adverse events from clinical trials and post-marketing surveillance. If you are looking for an exciting career where you can use your expertise and grow further, this is the opportunity for you. If you have experience as a Drug Safety Specialist, this role will be a great fit for you.
Responsibilities:
- Manage incoming calls related to clinical safety, ensuring all information is accurately recorded.
- Collect, process, and track adverse and serious adverse events from various sources, ensuring all data is correctly documented.
- Write detailed safety narratives and reports to accurately reflect safety data and findings.
- Report on various safety data, identifying trends and providing insights to improve safety processes.
- Work closely with internal departments and investigative clinical research sites to ensure compliance with safety processes and protocols.
Qualifications:
- Bachelor’s degree in Nursing, Pharmacy, Pharmacology, or a related healthcare field.
- Experience in clinical research, case processing, or post-marketing pharmacovigilance is preferred.
- Proficient in English, both spoken and written.
- Good knowledge of Microsoft Office, including Word, Excel, and PowerPoint.
- Broad understanding of medical terminology and its application in clinical safety.
- Strong organizational and communication skills, with the ability to work effectively in a team environment.
About Medpace:
Medpace is a global, full-service clinical contract research organization (CRO) that provides 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 through a scientific and disciplined approach.
Our Services:
- We offer a comprehensive range of services for clinical trials, from early-phase development to post-marketing surveillance.
- Our regulatory experts provide strategic guidance to navigate complex regulatory environments globally.
- We support medical communication and education to ensure the dissemination of important clinical data.
Key Therapeutic Areas:
- Developing treatments for various types of cancer.
- Advancing therapies for heart diseases.
- Focusing on conditions like diabetes and obesity.
- Addressing hormonal disorders.
- Innovating treatments for neurological conditions.
- Working on therapies for infectious diseases.
Global Reach:
- Based in Cincinnati, Ohio.
- Employing more than 5,000 people across 40+ countries.
- Leveraging local regulatory and therapeutic expertise across major regions.
Why Join Medpace?
Medpace offers a unique working environment that fosters growth and development. Here are some reasons why you should consider joining us:
- The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families. The work we do today will improve the lives of people living with illness and disease in the future.
- We offer structured career paths with opportunities for professional growth and development. You can expand your skills and take on new challenges in a supportive environment.
- We understand the importance of work-life balance. We offer hybrid work-from-home options, a flexible work schedule, and competitive PTO packages to help you manage your personal and professional life.
- We value our employees and recognize their contributions. We host company-sponsored employee appreciation events to celebrate our team’s hard work and dedication.
- Your well-being is important to us. We offer employee health and wellness initiatives to support your physical and mental health.
Competitive Compensation and Benefits:
- We offer a competitive compensation package that reflects your skills and experience.
- Our benefits package includes health insurance, retirement plans, and other perks to support your overall well-being.
Awards and Recognition:
- Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023, and 2024.
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
Apply Today and Make a Difference Tomorrow!
Joining Medpace means being part of a team that is dedicated to improving patient lives through innovative clinical research. If you are passionate about clinical safety and want to make a difference, apply today to become our next Clinical Safety Coordinator. This role is perfect if you have experience as a Drug Safety Specialist. Together, we can shape the future of medical therapeutics and make a lasting impact on global health.
Helpful Links:
How Pharmacovigilance Interviews Are Conducted
Pharmacovigilance Interview Questions PDF 2024
By joining our team as a Clinical Safety Coordinator, you will be stepping into a role similar to that of a Drug Safety Specialist, with opportunities to grow and develop your career.