Job Title: Associate Medical Reviewer
Job Category: Clinical Development | Clinical Research | Medical Monitoring
Location: Bengaluru (Bangalore), Karnataka, India
Department: Central Monitoring Unit (CMU), Global Business Services
Employment Type: Full-Time
Experience Required: 1–2 Years
Application Deadline: 15 January 2026
ThePharmaDaily.com is featuring an excellent career opportunity for an Associate Medical Reviewer within a leading global pharmaceutical organization. This role is ideal for medical professionals passionate about patient safety, clinical trial quality, and medical monitoring within regulated clinical research environments.
As part of the Central Monitoring Unit (CMU), you will play a critical role in ensuring the accuracy, consistency, and medical integrity of clinical trial data while supporting global clinical development programs.
Perform comprehensive medical review of clinical trial subjects to ensure high-quality, consistent, and reliable medical data
Monitor patient safety and ensure adherence to study protocols, Good Clinical Practice (GCP), ICH guidelines, local regulations, and internal SOPs
Identify medical inconsistencies, safety signals, and data discrepancies within clinical trial datasets
Collaborate with investigational site staff and healthcare professionals to resolve medical concerns
Identify clinically significant outliers and ensure protocol compliance
Present medical review findings to Medical Specialists to support informed decision-making
Perform medical monitoring activities, including risk-based monitoring and data consistency checks
Maintain detailed documentation of all medical review activities to ensure continuous inspection readiness
Work closely with Data Managers, Trial Managers, Medical Specialists, and global stakeholders
Stay updated on therapeutic area knowledge, protocol-specific requirements, and evolving medical developments
Mandatory Qualifications
MBBS with MD qualification
1–2 years of experience in clinical practice or academic medicine
Strong knowledge of ICH-GCP guidelines and clinical research standards
Excellent understanding of medical terminology and clinical trial processes
Familiarity with risk-based monitoring methodologies
Experience with clinical trial data systems and monitoring tools
Proficiency in MS Office tools including Word, Excel, PowerPoint, and MS Project
Strong analytical, problem-solving, and result-oriented mindset
Ability to manage complex tasks independently with strong planning skills
Excellent written and verbal communication skills in English
Effective stakeholder management and collaboration abilities
The Central Monitoring Unit in Bengaluru is part of the Clinical Drug Development function and brings together medical professionals and technical experts to support centralized clinical trial monitoring. Medical Reviewers collaborate closely with global Medical Specialists to ensure patient safety, protocol compliance, and high-quality data delivery. The team leverages advanced analytics, visualization tools, and statistical monitoring to proactively identify risks and improve trial outcomes.
Opportunity to contribute directly to global clinical trials and patient safety
Collaborative, science-driven work culture with global exposure
Strong focus on quality, compliance, and continuous learning
Be part of an organization committed to improving long-term health outcomes worldwide
The organization is committed to inclusive recruitment and equal opportunity for all applicants. No recruitment-related fees are charged, and unsolicited job offers should be treated with caution. Official communication will always follow standard recruitment practices.
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
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Baddi | Solan |Rajasthan :
Banasthali | Bhiwadi | Jaipur | Pilani | Udaipur |Karnataka :
Bangalore | Belgaum | Bengaluru | B.G Nagara | Bommasandra | Colorado | Czech Republic | Karnataka | Mangaluru | Mysore | Udupi |Punjab :
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Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Tallinn |Hà Nội :
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Springville | Belgium | Xzagreb | Slovakia | Bountiful | Regulatory Labeling Manager (NA and LATAM Only) | Bishop | Castlebar | Lenexa | Leinster | Nairobi | Riga | McFarland | Remote - Europe | Lousiana | Ireland | Green Way | Texas | Faridabad | Blue Bell | Remote, USA | Switzerland | Manipal | Medan | Tulsa | French | Victoria | Zaragoza | Remote - South America (Latin Americal) | Minnesota | Hungary | Remote - Africa | Melbourne | Remote - Middle East | Thailand | Remote | Hammond |Republic of Colombia :
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Kyiv |Lima Region :
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