Medpace, a global full-service Clinical Research Organization (CRO), is at the forefront of clinical development services for biotechnology, pharmaceutical, and medical device industries. With over 30 years of experience and operations spanning 40+ countries, Medpace is dedicated to accelerating the global development of safe and effective medical therapeutics. Recognized by Forbes and Life Science Leader magazine for its expertise and quality, Medpace offers a vibrant work environment that emphasizes people, purpose, and passion.
Responsibilities in Job
As a Clinical Safety Coordinator, you will play a critical role in safeguarding patient safety by ensuring the efficient handling and processing of adverse events. Key responsibilities include:
- Developing action plans for managing incoming calls.
- Collecting, processing, and tracking adverse and serious adverse events.
- Writing comprehensive safety narratives.
- Reporting on various safety data metrics.
- Collaborating with internal teams and clinical research sites to ensure adherence to safety protocols.
Qualifications
To excel in this role, candidates should possess the following:
- Educational Background: A Bachelor’s degree in a healthcare-related field, such as Nursing, Pharmacy, or Pharmacology.
- Experience: Preferred experience in clinical settings, clinical research, case processing, or post-marketing pharmacovigilance.
- Technical Skills: Proficiency in Microsoft® Office and a strong grasp of medical terminology.
- Language Proficiency: Advanced English skills are essential.
- Other Attributes: Strong organizational and communication abilities.
Skills Required
- Deep understanding of medical terminology.
- Exceptional organizational skills for managing detailed safety processes.
- Effective communication skills for collaboration with diverse teams.
- Analytical skills to process safety data and create accurate narratives.
- Technical proficiency with standard software tools like Microsoft® Office.
