Pharmacovigilance Jobs at Emmes Group – Pharma Jobs in Bengaluru for Safety Monitor II
Pharmacovigilance Jobs at Emmes Group present an excellent opportunity for professionals seeking advanced Pharma Jobs in Bengaluru within medical safety and clinical research. This Safety Monitor II role supports critical pharmacovigilance activities while ensuring patient safety, regulatory compliance, and global clinical research standards. Candidates interested in long-term growth in Pharmacovigilance Jobs and high-impact Pharma Jobs in Bengaluru will find this role highly rewarding.
Job Details
- Job Title: Safety Monitor II
- Location: Bengaluru, India
- Job ID: 2764
About the Company
Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Founded more than 47 years ago, Emmes Group became one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma.
Emmes has built industry-leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. These Pharmacovigilance Jobs reflect Emmes Group’s commitment to innovation, collaboration, and excellence, making it a trusted employer for professionals seeking long-term Pharma Jobs in Bengaluru.
Job Description | Pharmacovigilance Jobs
The Safety Monitor II role within Pharmacovigilance Jobs involves implementing Pharmacovigilance activities in collaboration with the Pharmacovigilance and Medical Monitoring (PMM) department under direct supervision.
This position assists senior Safety Monitors with interventional and non-interventional clinical projects alongside Medical Monitors and project teams. The role supports the design and execution of PV-related projects, including management of local and international PV systems, Real World Evidence projects, and adherence to Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GVP), making it a key opportunity among Pharma Jobs in Bengaluru.
Key Responsibilities
- Assist in safety monitoring activities with Medical Monitors and project teams
- Review safety events and adverse drug reaction cases from all sources
- Provide first-line evaluation of serious adverse events (SAEs)
- Communicate with site staff to collect additional AE and SAE information
- Prepare SAE narratives for DSMB reports, regulatory submissions, and study reports
- Coordinate timely reporting to regulatory authorities and partners
- Maintain and reconcile SAE databases
- Review adverse events, toxicities, concomitant medications, and medical history
- Participate in DSMB and safety review committee meetings
- Contribute to the safety sections of protocols, reports, and safety documents
- Perform MedDRA and WHO Drug coding
- Support audits, quality assurance, and SOP compliance
- Maintain accurate regulatory reporting to FDA, EMA, and other authorities
- Complete required training and support corporate safety initiatives
Qualifications Required for Pharmacovigilance Jobs
- Bachelor’s degree in pharmacology, or other scientific discipline (required)
- Experience in clinical practice is preferred
- Experience in safety monitoring or pharmacovigilance is preferred
