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Curriculum vitae
Clinical Research - Project Management – 5 years of experience
Zubin
Ashraf
Mob:
+918281430097
E-mail:
zubin.ashraf@gmail.com
Personal details
Name Zubin Ashraf
Fathers name E.M. Ashraf
Date of Birth 14-July-1986 (Age 28 years)
Permanent Address
Edappakath, Near Korjan U.P. School,
Kakkad Road, Kannur – 670005, Kerala,
India
Education B.Sc. Microbiology
M.Sc. Biochemistry
Languages known English, Hindi, and Malayalam.
Academic details
Class/Branch Board /
University
School / College City / State Grade /
Percentage
Year of
Passing
Class X
(S.S.L.C)
Kerala state
board
ST. Michaels
A.I.H.S.S.
Kannur, Kerala 85.16 % Mar-2002
Class XII
(
Higher Secondary
Examination)
Kerala state
board
ST. Michaels
A.I.H.S.S. Kannur, Kerala 77.33%
Mar-2004
Graduation
(B.Sc.
Microbiology)
Kannur
University
Sree Narayana
College
Kannur, Kerala First Class Mar-2007
Post- Graduation
(M.Sc.Biochemistry)
Bangalore
University
Garden City
College
Bangalore,
Karnataka
First Class Sept-2009
 Work Experiences
1. Molecular Connections, Bangalore, India ( Feb/2010 to Jun/2010 )
• Worked as Scientific Analyst at Molecular Connections Pvt. Ltd., Bangalore.
2. Quintiles Transnational, Bangalore, India
 Clinical Data Entry Experience (Sep/2010 to Feb2011 )
• Worked as Clinical Data Assistant (CDA 1) at Quintiles transnational, Bangalore on
contract basis from
• Working knowledge in ORACLE CLINICAL 4.5. CLINTRIAL and, INFORM Databases
• Well trained in Data Entry, CRF designing, Patient Enrollment, Batch Data load etc
• Always adhered to GCP guidelines and other Standard operating procedures (SOP’S) while
performing different tasks.
• Handled Multiple Projects and took lead role during Project lock and during the absence of
Project Manager.
• Promoted as Clinical Data Coordinator (ACDC) to Data validation team and became the
regular employee at Quintiles transnational, Bangalore.
 Clinical Data Validation Experience (Mar/2011 to Jun /2012)
• Worked as Clinical Data Coordinator (ACDC) at Quintiles transnational, Bangalore.
• Working Experience in RAVE and Inform Database.
• Worked as a good supporting team member for different projects.
• Handled multiple projects and involved in multiple activities from project GO-Live to project
Lock such as Document preparations and other project related activities assigned by the project
Manager.
• Always adhered to GCP guidelines and other Standard operating procedures (SOP’S) while
performing different tasks.
• Achieved Special Achievement Awards for being an excellent performer twice.
• Performed different activities as :
 SAS Dataset validation
 Data Query Management
 Edit Checks testing
 UAT (User Acceptance Test)
 Manual QC/QR and DB locking activities
 DVS Creation etc.
3. Icon Clinical Research, Trivandrum, Kerala, India
 Clinical Data coordinator 1 and 2 (09-Jul-2012 to 31-Mar-2014)
• Clinical Data coordinator 1 (CDC 1): 09-Jul-2012 to 31-Mar-2013
• Clinical Data coordinator 2 (CDC 2): 01-Apr-2013 to 31-Mar-2014
• Performed different DM related activities in Phase 1 trials (including Oncology trials) in
various therapeutic areas.
• Expert in DVS creation, Database testing, UAT, Data validation, Documentation and various
other activities in Clinical Research (Project Management) domain
 Lead Data Manager (01-Apr-2014 to Present)
• Currently working as 'Lead Data Manager' at Icon Clinical research.
• Responsibilities include creating SSP's (DVS/ DEI/DMP etc.) for assigned studies.
• Support Project leads (DMPL) in the execution, delivery and achievement of project milestones
on assigned projects.
• Regular communication with internal and external team – e.g. Site, Sponsor, external Labs etc.
• Provide Database training to the internal and external team as CRA, Medical monitors etc.
• Provide independent project leadership and serve as a resource for projects, deliverables and
improvement initiatives in the data management departments.
• Coordinate data management resources and activities for assigned studies to ensure that study
deliverables are achieved on time and to the highest quality.
I hereby declare that the above furnished information is correct and true to the best of my
knowledge and belief.
Zubin Ashraf

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Zubin_Ashraf_Resume

  • 1. Curriculum vitae Clinical Research - Project Management – 5 years of experience Zubin Ashraf Mob: +918281430097 E-mail: zubin.ashraf@gmail.com Personal details Name Zubin Ashraf Fathers name E.M. Ashraf Date of Birth 14-July-1986 (Age 28 years) Permanent Address Edappakath, Near Korjan U.P. School, Kakkad Road, Kannur – 670005, Kerala, India Education B.Sc. Microbiology M.Sc. Biochemistry Languages known English, Hindi, and Malayalam. Academic details Class/Branch Board / University School / College City / State Grade / Percentage Year of Passing Class X (S.S.L.C) Kerala state board ST. Michaels A.I.H.S.S. Kannur, Kerala 85.16 % Mar-2002 Class XII ( Higher Secondary Examination) Kerala state board ST. Michaels A.I.H.S.S. Kannur, Kerala 77.33% Mar-2004 Graduation (B.Sc. Microbiology) Kannur University Sree Narayana College Kannur, Kerala First Class Mar-2007 Post- Graduation (M.Sc.Biochemistry) Bangalore University Garden City College Bangalore, Karnataka First Class Sept-2009
  • 2.  Work Experiences 1. Molecular Connections, Bangalore, India ( Feb/2010 to Jun/2010 ) • Worked as Scientific Analyst at Molecular Connections Pvt. Ltd., Bangalore. 2. Quintiles Transnational, Bangalore, India  Clinical Data Entry Experience (Sep/2010 to Feb2011 ) • Worked as Clinical Data Assistant (CDA 1) at Quintiles transnational, Bangalore on contract basis from • Working knowledge in ORACLE CLINICAL 4.5. CLINTRIAL and, INFORM Databases • Well trained in Data Entry, CRF designing, Patient Enrollment, Batch Data load etc • Always adhered to GCP guidelines and other Standard operating procedures (SOP’S) while performing different tasks. • Handled Multiple Projects and took lead role during Project lock and during the absence of Project Manager. • Promoted as Clinical Data Coordinator (ACDC) to Data validation team and became the regular employee at Quintiles transnational, Bangalore.  Clinical Data Validation Experience (Mar/2011 to Jun /2012) • Worked as Clinical Data Coordinator (ACDC) at Quintiles transnational, Bangalore. • Working Experience in RAVE and Inform Database. • Worked as a good supporting team member for different projects. • Handled multiple projects and involved in multiple activities from project GO-Live to project Lock such as Document preparations and other project related activities assigned by the project Manager. • Always adhered to GCP guidelines and other Standard operating procedures (SOP’S) while performing different tasks. • Achieved Special Achievement Awards for being an excellent performer twice. • Performed different activities as :  SAS Dataset validation  Data Query Management  Edit Checks testing
  • 3.  UAT (User Acceptance Test)  Manual QC/QR and DB locking activities  DVS Creation etc. 3. Icon Clinical Research, Trivandrum, Kerala, India  Clinical Data coordinator 1 and 2 (09-Jul-2012 to 31-Mar-2014) • Clinical Data coordinator 1 (CDC 1): 09-Jul-2012 to 31-Mar-2013 • Clinical Data coordinator 2 (CDC 2): 01-Apr-2013 to 31-Mar-2014 • Performed different DM related activities in Phase 1 trials (including Oncology trials) in various therapeutic areas. • Expert in DVS creation, Database testing, UAT, Data validation, Documentation and various other activities in Clinical Research (Project Management) domain  Lead Data Manager (01-Apr-2014 to Present) • Currently working as 'Lead Data Manager' at Icon Clinical research. • Responsibilities include creating SSP's (DVS/ DEI/DMP etc.) for assigned studies. • Support Project leads (DMPL) in the execution, delivery and achievement of project milestones on assigned projects. • Regular communication with internal and external team – e.g. Site, Sponsor, external Labs etc. • Provide Database training to the internal and external team as CRA, Medical monitors etc. • Provide independent project leadership and serve as a resource for projects, deliverables and improvement initiatives in the data management departments. • Coordinate data management resources and activities for assigned studies to ensure that study deliverables are achieved on time and to the highest quality. I hereby declare that the above furnished information is correct and true to the best of my knowledge and belief. Zubin Ashraf