Medical Reviewer / Medical Reviewer - Trainee

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  "language": "en",
  "location": {
    "raw": "Mysore, Karnataka, 570001, India",
    "city": "Mysore",
    "region": "Karnataka",
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    "confidence": 0.8
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  "inferred_at": "2026-06-19T10:29:03.214Z",
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  "list_job": {
    "id": "469",
    "isRemote": null,
    "location": {
      "city": "Mysore",
      "state": "Karnataka"
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    "departmentId": "18580",
    "locationType": "2",
    "jobOpeningName": "Medical Reviewer / Medical Reviewer - Trainee",
    "departmentLabel": "Drug Safety Services",
    "employmentStatusLabel": "Full-Time"
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  "detail_job_opening": {
    "location": {
      "city": "Mysore",
      "state": "Karnataka",
      "postalCode": "570001",
      "addressCountry": "India"
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    "datePosted": "2026-06-16",
    "atsLocation": {
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    "description": "<p><br>Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have<br>experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled<br>solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III<br>clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all<br>stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation.<br><br>DESCRIPTION:<br>Medical Reviewer is the key contact person for assigned clinical development or marketed products,<br>responsible for safety strategy and major safety deliverables, including both early and late-stage development,<br>as assigned. He/she is accountable for safety and risk management activities for one or more assigned<br>products. He/she will manage cross-functional assessment of benefit-risk profile and communication of safety<br>information for assigned product(s). The individual will be an integral part of a group of safety professionals<br>within Sitero and will closely collaborate with safety teams in Contract Research Organizations (CROs) and<br>partners. He/she will need to maintain medical knowledge as required by the role, strong and current<br>knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance<br>and risk-management practices.<br>ESSENTIAL DUTIES AND RESPONSIBILITIES:<br>• Analyzes, reviews, and interprets safety data, both non-clinical and clinical.<br>• Performs medical review of ICSRs, and other drug safety information from multiple sources,<br>including clinical trials, spontaneous and solicited reports, aggregate and literature reports.<br>• Provides technical and medical expertise in medical assessment of causality of Individual Case<br>Safety Report (ICSR) as necessary, including the assessment of quality within the ICSR process;<br>identifies process improvement opportunities and drives changes.<br>• Contributes to the generation of aggregate safety reports including development safety update<br>reports, periodic benefit risk evaluation reports, and provide medical input in review of new or<br>existing safety documents to ensure compliance with relevant regulatory requirements.<br>• Contributes to the development of Standard Operating Procedures, Working Instructions and<br>other guidance documents.<br>• Contributes to safety and pharmacovigilance training programs.<br>• Provides safety training at investigator meetings.<br>• Collaborates with Regulatory Affairs to ensure appropriate reporting of pharmacovigilance and<br>drug safety information to regulatory agencies and prescriber community.<br>• Serves as a subject matter expert for vendors providing drug safety and pharmacovigilance<br>services.<br>• Training and mentoring of Pharmacovigilance Physicians and Specialists.<br>• Demonstrates knowledge and ensure compliance with current and applicable global PV<br>regulations and guidelines (e.g., CIOMS, FDA, PMDA, EMA, ICH, etc.).<br>EDUCATION AND EXPERIENCE REQUIRED:<br>0-3 years’ experience in Clinical Practice required. 1+ yr of experience in Drug Safety and<br>Pharmacovigilance in pharmaceutical or biotech company, CRO or regulatory agency within<br>Drug Safety/Pharmacovigilance, with both investigational and marketed products is preferable.<br>• Medical Degree (MBBS or higher) from recognized medical school.<br>PREFERRED SKILLS:<br>• Good working knowledge of US and EU drug safety regulations, CIOMS and ICH guidelines.<br>• Demonstrated experience with medical drug safety assessments, drug safety surveillance and<br>monitoring activities.<br>• Proficiency with medical review of ICSRs, including coding and use of SMQs, expectedness<br>assessments, causality assessments, narrative review and generation of Analysis of Similar Event<br>and company comment statements, including benefit-risk assessment.<br>• Experience with safety data collection and interpretation originating from clinical trials and<br>other sources (such as literature, solicited and post-marketing environment).<br>• Ability to build relationships, collaborate and influence across disciplines within Sitero and with<br>outside stakeholders.<br>• Excellent verbal, written and presentation skills.<br>• Innovative, collaborative, initiative-taker.<br>COMPENSATION &amp; BENEFITS:<br>Sitero proudly offers an impressive compensation package and benefits, including a competitive salary,<br>Variable pay, paid time off, and healthcare and retirement benefits.<br>EMPLOYMENT TYPE:<br>Permanent, Full Time<br>COMMITMENTS:<br>• Standard Hours 40 hours per week, one hour lunch, Monday – Friday. Additional hours as<br>needed.<br>• Willing to work in shifts as and when needed.<br>DISCLAIMER:<br>Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive<br>consideration for employment without discrimination on the basis of race, color, religion, sex, sexual<br>orientation, gender identity, national origin, protected veteran status, disability, or any other factors<br>prohibited by law.</p>",
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    "departmentId": "18580",
    "locationType": "2",
    "seekPromoted": false,
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    "jobOpeningName": "Medical Reviewer / Medical Reviewer - Trainee",
    "departmentLabel": "Drug Safety Services",
    "jobOpeningStatus": "Open",
    "minimumExperience": "Entry-level",
    "jobOpeningShareUrl": "https://sitero.bamboohr.com/careers/469",
    "employmentStatusLabel": "Full-Time"
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