Clinical Research Job at Medpace
Looking for a clinical research job in the clinical research industry? Medpace is hiring a full-time Clinical Safety Coordinator in Navi Mumbai, India. This is an excellent opportunity for healthcare professionals interested in Pharmacovigilance Jobs Mumbai and rewarding Medical Jobs in India. Join a globally recognized Contract Research Organization (CRO) and contribute to patient safety by supporting clinical trials and post-marketing drug safety activities.
About Medpace:
Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. With a mission to accelerate the global development of safe and effective medical therapeutics, Medpace leverages local regulatory and therapeutic expertise across major areas, including oncology and cardiology. Headquartered in Cincinnati, Ohio, Medpace employs over 6,000 people across more than 40 countries.
Job Details:
- Location: Navi Mumbai, India
- Job Reference Number: 11946
Job Description:
Medpace is inviting applications for a Clinical Research Job through its Clinical Safety Coordinator position in Navi Mumbai. The selected candidate will be responsible for processing adverse events received from clinical trials and post-marketing surveillance while ensuring compliance with global pharmacovigilance standards. The role involves writing safety narratives, reporting safety data, collaborating with investigative sites and internal departments, and supporting patient safety initiatives. This opportunity is ideal for candidates looking for Pharmacovigilance Jobs Mumbai and long-term Medical Jobs in India within a global CRO.
Key Responsibilities for this Clinical Research Job:
- Determine the 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
- Clinical experience or experience in Clinical Research, case processing, and post-marketing pharmacovigilance is preferred.
- Proficient English language skills are required.
- Proficient knowledge of Microsoft Office.
- Broad knowledge of medical terminology.
- Strong organisational and communication skills.
Skills Required for this Clinical Research Job:
- Strong understanding of pharmacovigilance principles.
- Knowledge of adverse event and serious adverse event processing.
- Broad understanding of medical terminology.
- Excellent organizational and time-management skills.
- Strong verbal and written communication skills.
- Ability to work collaboratively with cross-functional teams.
- Attention to detail and documentation accuracy.
- Ability to prioritize work in a fast-paced clinical research environment.
