Associate Medical Reviewer
Department: Clinical Development – Central Monitoring Unit (CMU)
Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Experience Required: 1–2 Years
Education: MBBS + MD
Industry: Pharmaceutical / Biotechnology / Clinical Research
Position Overview
We are seeking a highly motivated and detail-oriented Associate Medical Reviewer to join the Central Monitoring Unit (CMU). The successful candidate will play a critical role in ensuring patient safety, protocol compliance, and data quality across global clinical trials.
As an Associate Medical Reviewer, you will conduct comprehensive medical reviews of clinical trial data, identify potential safety concerns and data inconsistencies, collaborate with clinical trial stakeholders, and support medical monitoring activities throughout the study lifecycle.
This role offers an opportunity to work closely with Medical Specialists, Data Managers, Trial Managers, and cross-functional clinical development teams while contributing to the successful execution of clinical trials and the development of innovative therapies.
Key Responsibilities
Medical Data Review & Monitoring
Conduct detailed medical reviews of assigned clinical trial subjects to ensure data quality, consistency, and accuracy.
Evaluate clinical trial data for medical relevance, completeness, and protocol compliance.
Monitor patient safety throughout the clinical trial lifecycle.
Identify clinically significant findings, outliers, trends, and safety concerns requiring further investigation.
Assess adverse events, laboratory data, concomitant medications, and medical histories for consistency and accuracy.
Ensure compliance with study protocols, Good Clinical Practice (GCP), ICH Guidelines, local regulations, and company SOPs.
Medical Issue Resolution
Identify medical inconsistencies, discrepancies, and protocol deviations within clinical trial data.
Collaborate with investigational site personnel, healthcare professionals, and study teams to resolve data queries.
Escalate significant medical concerns and safety findings to Medical Specialists when appropriate.
Support root cause analysis and corrective actions for recurring data quality issues.
Clinical Trial Monitoring Support
Perform medical monitoring activities to support centralized monitoring efforts.
Conduct protocol compliance assessments across study sites.
Review clinically significant outliers and abnormal data patterns.
Support medical data cleaning activities and quality review processes.
Contribute to risk-based monitoring activities and centralized monitoring initiatives.
Stakeholder Collaboration
Present medical review findings and recommendations to Medical Specialists and study teams.
Collaborate closely with:
Medical Specialists
Data Managers
Trial Managers
Clinical Operations Teams
Central Monitoring Teams
Investigational Site Staff
Participate in discussions supporting clinical decision-making and study quality improvements.
Maintain effective communication with internal and external stakeholders.
Documentation & Compliance
Maintain accurate and complete documentation of all medical review activities.
Ensure inspection readiness and audit preparedness at all times.
Maintain records in accordance with regulatory requirements and internal procedures.
Contribute to quality assurance and compliance initiatives.
Continuous Learning & Knowledge Development
Stay current with:
Therapeutic area knowledge
Protocol-specific requirements
Medical and scientific developments
Clinical trial regulations and guidelines
Participate in training programs and professional development initiatives.
Contribute to knowledge sharing and best practice implementation within the team.
Required Qualifications
Education
Mandatory Qualification
MBBS (Bachelor of Medicine, Bachelor of Surgery)
AND
MD (Doctor of Medicine) in a relevant medical specialty
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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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 |Madhya Pradesh :
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Delhi | Gangtok | New Delhi | PAN-India |Assam :
Dibrugarh | Diburghar | Guwahati |West Bengal :
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Goa | Panaji | Verna |Bihar :
Hajipur | Patna |Kerala :
Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
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Ranchi |Sikkim :
Rangpo |India :
Remote, India | Siliguri |Illinois :
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Frank Scottile Blvd |Missouri :
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Berlin |Baden-Wurttemberg :
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Germany | GErmany |Lower Saxony :
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Saarbrucken |Switzerland :
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Belgrade | Serbia |Hungary :
Budapest |BULGARIA :
Bulgaria | Vedant |Denmark :
Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
Romania |Belgium :
Wavre |Tipperary :
Ballydine |Cork :
Brinny | Ringaskiddy |Carlow :
Carlow |Republic of Ireland :
Cork | Dublin | Limerick | Waterford |Ulster :
Donegal |Meath :
Dunboyne |Dún Laoghaire :
Dún Laoghaire |Galway :
Galway |County Dublin :
Swords |Republic of China :
Beijing |China :
China | Quarry Bay |Liaoning :
Dalian |Zhejiang :
Hangzhou |Tokiyo :
Osaka | Tokyo |Shanghai Sai :
Shanghai Shi |Hubei :
Wuhan |Capital of Netherland :
Amsterdam |North Brabant :
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Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
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Queensland |Melbourne :
South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
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Zaventem |South America :
Argentina | Peru |Brazil :
Sao paulo | Brazil |Attica :
Koropi | Athens |Greece :
Greece |North Island :
Auckland |New Zealand :
New Zealand |Austria :
Austria |Vienna :
Vienna |Catalonia :
Barcelona |Madrid :
Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Estonia | Tartu |Harju County (Maakond) :
Tallinn |Hà Nội :
Hà Nội | Hanoi |Ho Chi Minh :
Ho Chi Minh City |Italy :
Italy |Lombardy :
Rho |Jakarta :
Jakarta |East Java :
Surabaya |Japan :
Japan | Saitama |Tokyo :
Otemachi |North Ostrobothnia :
Oulu |Southwest Finland (Varsinais-Suomi) :
Turku |Remote Korea :
Remote Korea |Republic of Korea :
Seoul |Kazakhstan :
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Bangkok |Israel :
Yavne | Tel Aviv | Netanya | Be'Er Sheva | Kfar Saba |Remote :
Melbourne | Medan | Thailand | Belgium | French | Perth | Remote - Africa | Nairobi | Regulatory Labeling Manager (NA and LATAM Only) | Minnesota | Remote - Middle East | Blue Bell | Manipal | Leinster | Springville | Tulsa | Hungary | Zaragoza | Ireland | Texas | Riga | Victoria | Castlebar | Lousiana | Xzagreb | Milwaukee | Faridabad | McFarland | Switzerland | Bountiful | Slovakia | Lenexa | Remote - South America (Latin Americal) | Hammond | Green Way | Bishop | Remote - Europe |Republic of Colombia :
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Brentwood |Bucharest :
Bucharest |Buenos Aires :
Buenos Aires |Republic of Egypt :
Cairo |Mexico :
Ciudad de México | New Mexico |Dubai :
Dubai |Makkah :
Najran | Khulais | Rabigh | Riyadh | Jeddah | King Abdullah Economic City |Kuala Lumpur :
Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
Lima |France :
Lyon | Paris |South Africa :
South Africa | Midrand |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
Sarajevo |Singapore :
Singapore |Sofia City :
Sofia |Sweden :
Sweden |Taipei :
Taipei |Mazovia :
Warsaw |