Associate Manager, Clinical Data Management

Hyderabad, INPosted Jul 6, 2026
Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsAssociate Manager, Clinical Data ManagementHyderabad - TS - IN No longer accepting applications.Job IDR1602850Date posted05/26/2026DepartmentData ManagementResponsibilities will include, but are not limited to: Study Startup:  Draft EDC build timeline in collaboration with Data Management Lead.  Perform DB build tasks by creating specifications for Database and Edit Checks.  Create test scripts and complete test data entry/UAT for Coding, Site Payment, Safety Gateway.  Collaborate with Data Management Lead and facilitate startup meetings which includes, not limited to, EDC build kick-off, Interactive eCRF Build and IRMs (Interactive Review Meeting) for database and Edit checks.  Create and finalize study documents like Data Quality Management Plan, eCRF completion Instructions, Protocol Data Review Plan (PDRP) post study team review.  Ensure all startup documents are completed as per SOP and filled in eTMF as per eTMF master plan. Study Conduct:  Plan/execute Post Production/Migration for the study (if any).  Coordinate with Clinical Data Managers for the execution of data review tasks.  Coordidate with external data vendors for any escalations related to any vendor data.  Support Clean Patient Group delivery along with Clinical Data Management staff.  Update study documents as needed during the conduct of the study  Support DML to coduct Data Quality Review meetings.  Provide Data Health Metrics to Data Management Lead as requested. tudy Closeout-  Support Data Management Lead in planning and execution of database lock activities.  Perform post lock activities, as needed. Project Management  Support DML in project management tasks to make sure that study is delivered successfully as per the study timelines with quality. Documentation:  Filing of appropriate documents in eTMF as per eTMF master plan. Training and Mentorship:  Provide Training and mentoring to junior CDM staff.Responsibilities :will include, but are not limited to: Study Startup:  Draft EDC build timeline in collaboration with Data Management Lead.  Perform DB build tasks by creating specifications for Database and Edit Checks.  Create test scripts and complete test data entry/UAT for Coding, Site Payment, Safety Gateway.  Collaborate with Data Management Lead and facilitate startup meetings which includes, not limited to, EDC build kick-off, Interactive eCRF Build and IRMs (Interactive Review Meeting) for database and Edit checks.  Create and finalize study documents like Data Quality Management Plan, eCRF completion Instructions, Protocol Data Review Plan (PDRP) post study team review.  Ensure all startup documents are completed as per SOP and filled in eTMF as per eTMF master plan. Study Conduct:  Plan/execute Post Production/Migration for the study (if any).  Coordinate with Clinical Data Managers for the execution of data review tasks.  Coordidate with external data vendors for any escalations related to any vendor data.  Support Clean Patient Group delivery along with Clinical Data Management staff.  Update study documents as needed during the conduct of the study  Support DML to coduct Data Quality Review meetings.  Provide Data...

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