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CURRICULUM VITAE
SRAVAN AKUMALLA Email: sra1.king@gmail.com
Clinical Data Analyst Phone No: +91-7569888686
SUMMARY
 Having 1 Year of experience in the field of Clinical Data Management and having
thorough understanding on Clinical trial Phases, Clinical trial process and Clinical data
management process.
 Proficient in Oracle Clinical Data Base, and Hands-on experience on Conduct Phase.
 Good understanding on ICH-GCP and Medical Terminology.
 Knowledge on clinical trial procedures and clinical practice standards of Food and Drug
Administration (FDA).
 Good understanding on CDISC guidelines.
 Good understanding on 21 CFR Part 11 and Good Clinical Data Management Practice
(GCDMP).
 Understanding on SOP’s.
PROFESSIONAL EXPERIENCE
Presently Working for Phase Clinica Life Sciences Pvt Ltd., as a Clinical Data Analyst from
(April 2015 – Till Date), Hyderabad.
Roles and Responsibilities:
Data Management:
 Data Management Plan
 Writing Edit Checks Specifications
 Creating Clean and Dirty Subjects
 Informal Testing
 Data Entry Screen Testing
 Complete UAT Process
 CRF Receipt and Tracking of Missing / Pending pages
 Manual Review of CRFs
 Double Data Entry Process
 Running Batch Validation
 Discrepancy Management and Query Tracking
 Printing DCF
 Resolving DCFs
 Re-query Management
 Quality Control of Clinical Trial Data
Other Responsibilities:
 Deliver best value and high quality service.
 Check own work in an ongoing way to ensure first-time quality.
 Review and resolve data discrepancies identified by the system or through manual checks
as identified in the data editing guidelines.
 Support multiple clinical trials, across diverse therapeutic areas, to successful conclusion
and provide technical oversight when required.
 Keep manager informed about work progress and any issues to avoid surprises.
 Keeps regular interaction and supervision by Manager or assigned mentor.
ACADEMIC QUALIFICATIONS
 Bachelor of Pharmacy 2012-2015 from Mohammadiya Institute Of Pharmacy,
Khammam, with 73.5%.
 Board of Intermediate 2009 - 2011 from Roa’s Junior college , Nandyala with 75%.
 C.B.S.E from Jawahar Navodaya Vidyalaya , Kurnool, with78%
PERSONAL PROFILE
Father’s Name : Prem kumar
Age : 23yrs
Gender : Male
Marital Status : Unmarried
Nationality : Indian
Languages known : English, Hindi and Telugu
Current Stay : Hyderabad
DECLARATION
I hereby declare that all the details furnished above are true to the best of my knowledge.
Place: Hyderabad (Sravan A)
Date :

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SRAVAN RESUME

  • 1. CURRICULUM VITAE SRAVAN AKUMALLA Email: sra1.king@gmail.com Clinical Data Analyst Phone No: +91-7569888686 SUMMARY  Having 1 Year of experience in the field of Clinical Data Management and having thorough understanding on Clinical trial Phases, Clinical trial process and Clinical data management process.  Proficient in Oracle Clinical Data Base, and Hands-on experience on Conduct Phase.  Good understanding on ICH-GCP and Medical Terminology.  Knowledge on clinical trial procedures and clinical practice standards of Food and Drug Administration (FDA).  Good understanding on CDISC guidelines.  Good understanding on 21 CFR Part 11 and Good Clinical Data Management Practice (GCDMP).  Understanding on SOP’s. PROFESSIONAL EXPERIENCE Presently Working for Phase Clinica Life Sciences Pvt Ltd., as a Clinical Data Analyst from (April 2015 – Till Date), Hyderabad. Roles and Responsibilities: Data Management:  Data Management Plan  Writing Edit Checks Specifications  Creating Clean and Dirty Subjects  Informal Testing
  • 2.  Data Entry Screen Testing  Complete UAT Process  CRF Receipt and Tracking of Missing / Pending pages  Manual Review of CRFs  Double Data Entry Process  Running Batch Validation  Discrepancy Management and Query Tracking  Printing DCF  Resolving DCFs  Re-query Management  Quality Control of Clinical Trial Data Other Responsibilities:  Deliver best value and high quality service.  Check own work in an ongoing way to ensure first-time quality.  Review and resolve data discrepancies identified by the system or through manual checks as identified in the data editing guidelines.  Support multiple clinical trials, across diverse therapeutic areas, to successful conclusion and provide technical oversight when required.  Keep manager informed about work progress and any issues to avoid surprises.  Keeps regular interaction and supervision by Manager or assigned mentor.
  • 3. ACADEMIC QUALIFICATIONS  Bachelor of Pharmacy 2012-2015 from Mohammadiya Institute Of Pharmacy, Khammam, with 73.5%.  Board of Intermediate 2009 - 2011 from Roa’s Junior college , Nandyala with 75%.  C.B.S.E from Jawahar Navodaya Vidyalaya , Kurnool, with78% PERSONAL PROFILE Father’s Name : Prem kumar Age : 23yrs Gender : Male Marital Status : Unmarried Nationality : Indian Languages known : English, Hindi and Telugu Current Stay : Hyderabad DECLARATION I hereby declare that all the details furnished above are true to the best of my knowledge. Place: Hyderabad (Sravan A) Date :