Medical Officer Job at Emmes Group, Bengaluru
Looking for a clinical research career where doctors can work beyond hospitals and directly impact global drug development? Emmes Group is hiring Medical Officers/Medical Monitors for its Bengaluru location, with hybrid and remote work options. This Medical Officer Job at Emmes Group in Bengaluru is ideal for MBBS or MD professionals interested in clinical research, pharmacovigilance, safety monitoring, and medical affairs. Candidates will work on global clinical trials, safety oversight, regulatory documentation, and medical strategy activities. It is an excellent opportunity for doctors who want to transition into the pharmaceutical and CRO industry.
About the Company:
Emmes Group is a global clinical research organization with more than 47 years of experience in advancing medical research and clinical development. The company initially worked closely with the US government and later expanded into partnerships with biopharma and healthcare organizations worldwide.
Emmes specializes in areas such as cell and gene therapy, vaccines, infectious diseases, ophthalmology, neuroscience, and rare diseases. The company focuses on innovation, patient-centered research, and improving healthcare outcomes through clinical trials and medical expertise.
Job Details:
- Job Role: Medical Officer / Medical Monitor
- Location: Bengaluru
- Work Mode: Hybrid / Remote
- Job Type: Full-Time
- Department: Pharmacovigilance & Medical Monitoring
- Experience Required: Minimum 2 Years
- Industry: Clinical Research / CRO / Pharmaceutical
Key Responsibilities:
- Perform medical monitoring for clinical trials
- Review safety and efficacy data for assigned protocols in this Medical Officer Job
- Evaluate adverse events and serious adverse event reports
- Review SAE narratives, DSURs, CIOMS reports, and MedWatch reports
- Support protocol development and study safety strategies in this Job in Bengaluru
- Advise study teams on inclusion/exclusion criteria and safety procedures
- Review MedDRA and WHO Drug coding activities at Emmes Group
- Participate in DSMB, DMC, and safety oversight committee meetings
- Collaborate with Safety Monitors, Project Leadership, and Data Management teams
- Support regulatory meetings and investigator training programs
- Assist in the preparation of safety monitoring plans and clinical study reports
- Participate in audits, SOP development, and quality assurance activities
- Support bid preparation and provide medical consultancy services
Educational Requirements for this Medical Officer Job:
Candidates with the following qualifications are eligible:
- MBBS
- MD
- MBBCh
- Equivalent Medical Degree
Candidates with clinical practice experience and exposure to pharmaceutical medicine, clinical research, pharmacovigilance, medical affairs, or regulatory activities are preferred.
Skills Required:
- Strong clinical and medical knowledge
- Understanding of clinical research and safety monitoring
- Knowledge of adverse event reporting and pharmacovigilance
- Experience with regulatory submissions and safety documents
- Excellent communication and presentation skills
- Ability to explain complex clinical concepts clearly
- Team collaboration and leadership abilities
- Knowledge of MedDRA coding and safety reporting systems
- Strong analytical and decision-making skills
- Ability to work in cross-functional global teams
Benefits of the Medical Officer Job:
- Opportunity to work in global clinical research projects
- Hybrid and remote work flexibility
- Exposure to pharmacovigilance and medical monitoring activities
- Experience with international regulatory and safety processes
- Career growth in CRO, Medical Affairs, and Clinical Research
- Opportunity to work with global pharmaceutical partners
- Involvement in scientific and regulatory meetings
- Collaborative and innovation-driven work environment
- Exposure to advanced therapeutic areas like gene therapy and rare diseases
