Associate Medical Data Review Manager
Location: Bangalore, India / Thane, Maharashtra, India
Employment Type: Full Time
Job Overview
The Associate Medical Data Review Manager is responsible for providing medical review expertise to support high-quality clinical data management deliverables. The role focuses on structured patient data review from a clinician's perspective, identifying medical anomalies, ensuring data plausibility and protocol compliance, and supporting clinical study teams with medical insights and project management expertise.
The position combines clinical knowledge, data review capabilities, project coordination, stakeholder management, and process improvement responsibilities within a clinical research environment.
Key Responsibilities
Medical Data Review
Perform structured medical review of patient-level clinical trial data.
Identify patient anomalies and inconsistencies within study datasets.
Assess medical congruency and plausibility of clinical data against study protocols.
Evaluate safety and efficacy data from a clinical perspective.
Review clinical data trends and escalate potential concerns when required.
Ensure high-quality and medically accurate data review outcomes.
Project Management & Study Support
Provide project management support for assigned studies.
Collaborate with:
Clinical Study Teams
Project Managers
Medical Monitors
Sponsors
Internal Functional Teams
Manage workload projections and project priorities.
Support issue tracking, escalation, and resolution activities.
Participate in process improvement initiatives to enhance operational efficiency.
Medical Expertise & Subject Matter Support
Serve as a Subject Matter Expert (SME) for medical review activities.
Provide clinical guidance to project teams.
Support interpretation of medical findings and study-specific data issues.
Deliver therapeutic area and indication-specific training to project teams.
Contribute medical expertise during study planning and execution.
Quality & Compliance
Ensure compliance with:
Study Protocols
Regulatory Requirements
Clinical Data Review Standards
Internal SOPs
Track and support resolution of compliance-related issues.
Maintain inspection-ready documentation and processes.
Support quality improvement initiatives.
Client & Stakeholder Management
Build and maintain strong customer relationships.
Participate in:
Kick-Off Meetings (KOM)
Weekly Study Team Meetings
Sponsor Meetings
Client Discussions
Communicate findings, risks, and recommendations effectively to stakeholders.
Process Improvement & Leadership
Identify opportunities to improve:
Data Review Efficiency
Process Quality
Project Delivery
Support root cause analysis and corrective action implementation.
Mentor and guide junior team members where required.
Contribute to continuous improvement initiatives within Medical Data Review operations.
Qualifications
Education
MBBS with a minimum of 2 years of relevant experience.
OR
MD (Any Specialization) – Freshers and experienced candidates may be considered.
Experience (Minimum Required)
Experience in:
Clinical Data Sciences
Clinical Research
Pharmaceutical Industry
CRO Environment
Medical Review Activities
Demonstrated leadership or project coordination experience preferred.
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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Delhi | Gangtok | New Delhi | PAN-India |Assam :
Dibrugarh | Diburghar | Guwahati |West Bengal :
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Hajipur | Patna |Kerala :
Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
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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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Ingelheim am Rhein | Mainz |Schleswig Holstein :
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Rostock |Saarland :
Saarbrucken |Switzerland :
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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 :
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Wavre |Tipperary :
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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 :
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Canada |Quebec :
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Brussels |Antwerp :
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Argentina | Peru |Brazil :
Sao paulo | Brazil |Attica :
Athens | Koropi |Greece :
Greece |North Island :
Auckland |New Zealand :
New Zealand |Austria :
Austria |Vienna :
Vienna |Catalonia :
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Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Estonia | Tartu |Harju County (Maakond) :
Tallinn |Hà Nội :
Hanoi | Hà Nội |Ho Chi Minh :
Ho Chi Minh City |Italy :
Italy |Lombardy :
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Jakarta |East Java :
Surabaya |Japan :
Saitama | Japan |Tokyo :
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Oulu |Southwest Finland (Varsinais-Suomi) :
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Seoul |Kazakhstan :
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Bangkok |Israel :
Be'Er Sheva | Tel Aviv | Netanya | Yavne | Kfar Saba |Remote :
Belgium | Perth | Leinster | Regulatory Labeling Manager (NA and LATAM Only) | Springville | Minnesota | Bountiful | Lousiana | Remote - Africa | Remote - Middle East | Faridabad | Xzagreb | Hungary | Medan | Slovakia | Remote - South America (Latin Americal) | Hammond | Victoria | Green Way | Nairobi | Lenexa | Switzerland | French | Castlebar | Ireland | Riga | Remote - Europe | Texas | Bishop | Blue Bell | Melbourne | Zaragoza | McFarland | Tulsa | Milwaukee | Manipal | Thailand |Republic of Colombia :
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Kyiv |Lima Region :
Lima |France :
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South Africa | Midrand |Nišava District :
Niš |Bohemia :
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