Prerit Barman
Senior Clinical Data Manager at Atlantia Food Clinical Trials- Claim this Profile
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Marathi Elementary proficiency
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English Full professional proficiency
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Hindi Full professional proficiency
Topline Score
Bio
Harish Sharma
Prerit is well organized, skilled and dedicated DM professional. It was a pleasure working with him. Good luck him in next project.
Vidya Pol
Prerit has a strong technical knowledge and project management skills. Being his supervisor while working at Cognizant, I was really impressed with his ability to never having issues meeting timelines and giving close attention to detail in all aspects of his work. His clinical data management knowledge would be a true asset for any position requiring end to end domain knowledge.
Harish Sharma
Prerit is well organized, skilled and dedicated DM professional. It was a pleasure working with him. Good luck him in next project.
Vidya Pol
Prerit has a strong technical knowledge and project management skills. Being his supervisor while working at Cognizant, I was really impressed with his ability to never having issues meeting timelines and giving close attention to detail in all aspects of his work. His clinical data management knowledge would be a true asset for any position requiring end to end domain knowledge.
Harish Sharma
Prerit is well organized, skilled and dedicated DM professional. It was a pleasure working with him. Good luck him in next project.
Vidya Pol
Prerit has a strong technical knowledge and project management skills. Being his supervisor while working at Cognizant, I was really impressed with his ability to never having issues meeting timelines and giving close attention to detail in all aspects of his work. His clinical data management knowledge would be a true asset for any position requiring end to end domain knowledge.
Harish Sharma
Prerit is well organized, skilled and dedicated DM professional. It was a pleasure working with him. Good luck him in next project.
Vidya Pol
Prerit has a strong technical knowledge and project management skills. Being his supervisor while working at Cognizant, I was really impressed with his ability to never having issues meeting timelines and giving close attention to detail in all aspects of his work. His clinical data management knowledge would be a true asset for any position requiring end to end domain knowledge.
Credentials
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Diploma in Clinical Data Management and SAS programming
Cliniminds, New Delhi IndiaJan, 2011- Nov, 2024
Experience
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Atlantia Clinical Trials
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Ireland
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Research Services
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1 - 100 Employee
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Senior Clinical Data Manager
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Aug 2020 - Present
•Data Operations Oversight for Projects/Program:•Discusses roadblocks with PM & management for completing study objectives in a timely manner•Act as an advisor to manage and collaborate with inter department (Project Management, Monitoring, Site Support, Regulatory etc.) on all data management aspects of projects with data components.•Identify and implement process improvement solutions.•Trains team members on specific departmental processes (Trial design document creation, Edit Check creation, CCB process, coding, database lock, etc.•Responsible for the hiring, promotion, transfer, and release of staff. Responsible to liaise with other functional counterparts as necessary to deliver successful projects/programs for the client•Liaise with sponsors on project related matters and timeline negotiations if required.
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Clinical Data Manager
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Sep 2017 - Aug 2020
•Managing setup and conduct activities for oncology and cardiovascular trials •Maintaining clinical data quality by focussing on discrepancy management and data review techniques.•Providing the operation team with database training.•User Access Management •Process improvement for data quality control •Managing setup and conduct activities for oncology and cardiovascular trials •Maintaining clinical data quality by focussing on discrepancy management and data review techniques.•Providing the operation team with database training.•User Access Management •Process improvement for data quality control
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IQVIA
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United States
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Hospitals and Health Care
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700 & Above Employee
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Senior Clinical Data Coordinator
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Dec 2016 - Aug 2017
•Data Operations Coordinator for two studies, handled mega oncology studies from set up to conduct phase.•Led the several clinical database lock.•Primary point of contact in data management for clients, vendors, database developers and programmers and clinical project managers•Assisting the Data Team Lead and project management team with the implementation and maintenance of the project quality plan, risk analysis, project resource management and managing the financial performance of the studies.•Responsible for the data management study budget and identification of any out of scope tasks.•Continuously reviewing processes to improve efficiency of tasks and quality of deliverables•Identify compliance issues and work with management to ensure timely follow-up and resolution•Track service performance to identify root causes of issues and implement corrective action plan•Weekly teleconferences with project management team to discuss project plan and timelines•Meet with Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables•Provided data management expertise as Subject Matter expert in a number of areas.•Generation and review of patient data listings, SDTM data ,Metadata and RECIST etc•Handling Third Party Reconciliation
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Cognizant
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United States
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IT Services and IT Consulting
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700 & Above Employee
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Clinical Data Manager-Quality Specialist
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Jul 2014 - Dec 2016
•CDM representative in cross functional study teams. •Handled Oncology Dermatology, Gastro intestinal studies simultaneously with great efficiency.• Performed extensive and sophisticated data capture techniques to ensure the generation of accurate, complete and consistent clinical databases.•Completion of automated dashboards in monthly data reviews as well as weekly metric formations for client evaluation.•Performing additional statistical and quantitative reviews of external data. •Mentoring team members, conducting protocol understanding and knowledge transfer sessions on a regular basis as well as monitoring their progress in order to establish projections and targets. Provide input to the performance appraisal process as requested•Co-ordinating with the study team for resolution of outstanding queries, reports and the routine follow up for updates on outstanding defects•Handling production defects and new client requests through a standard Change Request process•Participate in audits, conference calls with the study team•Tracking and reporting study defects via quality score cards on monthly basis•Heavily involved in Standard Operating Procedure review and SSP.
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Max Neeman International
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India
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Biotechnology
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100 - 200 Employee
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Associate Clinical Data Manager
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Feb 2013 - Jul 2014
•Handled Phase I, Phase II and Phase III of Clinical Trial• Extensive exposure of CDM databases such as Inform and Rave• Managed Set up, Conduct and Close Out activities• Set up activities- Creating edit/ manual checks, creating study specifications, developing test cases and performing UAT• Conduct activities- Query Management, External Data Reconciliation (ECG, IVRS and LAB), SAE Reconciliation, Manual review, Report and Listing review• Close out activities- Final data review and cleaning, contributed to timebound lock of the study. Handled post lock clinical documentation and archival process in compliance with the SOP and GCP •EDC coordination and Document réconciliation (CRFs and protocol)
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Process Associate - Clinical Data Management
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Oct 2011 - Jan 2013
•Database Designing•Data entry and database screen testing •Maintaining EDC trackers and working on IWRS for EDC studies.•Handling EDC services as a EDC helpdesk coordinator•Guest Lecturer at Apollo Healthcare Clinical Research Facility
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Quartesian | Now a Part of Veranex
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United States
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Pharmaceutical Manufacturing
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100 - 200 Employee
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Clinica Data Associate
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Jul 2011 - Oct 2011
Trained in Validation,Database designing and SAS activities Trained in Validation,Database designing and SAS activities
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Education
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2017 - 2018
National University of Ireland, Galway
Master's degree, Clinical Research -
2011 - 2012
Cliniminds, New Delhi India
Post graduate diploma in Clinical Data Management and SAS, Clinical Research -
2009 - 2011
University of Pune
Bachelor of Science (B.Sc.), Biotechnology -
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The Aditya birla Public School
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