Priyanka Agarwal

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PRIYANKA AGARWAL Mob: +91 9886845396 ● Email: [email protected] Objective: To get aligned with a reputed firm or company to get a deeper insight into the present education and utilize my skills and abilities in the industry that offers professional growth while being innovative and flexible. Proven record of consistent, excellent performance in Software Design, Development, Support and Maintenance services. Possess excellent interpersonal, communication and organisational skills. EMPLOYMENT HISTORY Have 8.4 years of relevant experience in the Clinical Data Management domain with Inform Tool(4.5/4.6/5.5/6.0/6.1)and Central Designer Version(1.4.4.0/1.4.4.1/2.0.3/2.1) iMedidata Certified. Currently working as Analyst with Quintiles Technologies from April 2014 till date. Worked as Programmer/Analyst with Quintiles Technologies from Oct 2012 to Mar-2013. Worked as Clinical Database Programmer,CDP with Quintiles Technologies from April 2011 to Sep-2012. Worked as Process expert(SME) with Accenture Services Pvt. Ltd, Bangalore from June 2008 till April 2011 in the Health and Life Sciences Department. TECHNICAL SUMMARY Technologies: Oracle InForm-4.5/4.6/5.5/6.0/6.1 (Architect & Central Designer(1.4.4.0/1.4.4.1/2.0/2.1)) SME(involves process and technology enhancement, issue resolution and library creation) eCRF design

Transcript of Priyanka Agarwal

Page 1: Priyanka Agarwal

PRIYANKA AGARWALMob: +91 9886845396 ● Email: [email protected]

Objective: To get aligned with a reputed firm or company to get a deeper insight into the present education and utilize my skills and abilities in the industry that offers professional growth while being innovative and flexible.

Proven record of consistent, excellent performance in Software Design, Development, Support and Maintenance services.

Possess excellent interpersonal, communication and organisational skills.

EMPLOYMENT HISTORY

Have 8.4 years of relevant experience in the Clinical Data Management domain with Inform

Tool(4.5/4.6/5.5/6.0/6.1)and Central Designer Version(1.4.4.0/1.4.4.1/2.0.3/2.1)

iMedidata Certified.

Currently working as Analyst with Quintiles Technologies from April 2014 till date.

Worked as Programmer/Analyst with Quintiles Technologies from Oct 2012 to Mar-2013.

Worked as Clinical Database Programmer,CDP with Quintiles Technologies from April 2011

to Sep-2012.

Worked as Process expert(SME) with Accenture Services Pvt. Ltd, Bangalore from June 2008 till

April 2011 in the Health and Life Sciences Department.

TECHNICAL SUMMARY

Technologies:Oracle InForm-4.5/4.6/5.5/6.0/6.1 (Architect & Central Designer(1.4.4.0/1.4.4.1/2.0/2.1))

SME(involves process and technology enhancement, issue resolution and library creation)

eCRF design

Edit Check programming

AUL generation and Updates / Admin activities

Home Page updates

IVRS/IWRS

RDE/TDE/CDD

Central Coding

Coding(includes Meddra and WhoDD)

SAS listings, Cognos Reports

Post production Changes(RWR, Study Version, Amendment changes,extension of studies)

Validation activities and process improvement

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Data Team Lead activities(involve protocol creation, interaction with clients, database cleaning and lock activities)

PROFESSION HISTORY

QUINTILES TECHNOLOGIES PVT. LTD., BANGALOREAnalyst, CDP

Current Responsibility:

1. Project Management and People Management – Currently Handling multiple clients with team of 8 people which involves project and resource allocation, responsible for their project delivery with good quality and timeline. Responsible for their performance appraisal and growth and development within the team.

2. Individual contributor: Work as an IC on projects related to Amendment and complex issue. Provide consulting to clients in various aspects of operations.

3. Trainer of CDM: Provides training of CDM to all new joiners and existing resources(onsite and offsite).

4. SME: An active member of Global SME team to formulate SOPs and processes for CDM operations. SME for issues resolution and consulting on Inform requirements.

ROLES AND RESPONSIBILITIES:

Leading the Project from the creation of database till the lock of Database, which involves communication with Sponsors, Study designers, CPM, and all the related parties. Review and creation of specifications.

Mentor the new joiners and provide Training on End to End Process. Worked mostly on the complex programming of edits with the Global team (ORACLE/INFORM

BUGS) related to dynamics/global condition and/or update workflow and/or repeating to repeating/add entry scenarios and was part of Global Support Team which involved the investigation of the errors and its workaround.

Conducted Meetings and forums where all the issues and solutions to be discussed and maintained a library. Create Guidelines and Documents.

Develop electronic case report forms (eCRF) for clinical data capture in Inform Architect / Central Designer.

Programming of Edit Checks in Inform Architect / Central Designer. Post Production Changes (RWR, Study Version) which includes Amendment changes(building

new study within the existing study) TDE/RDE Setup for Studies. Creation of HomePage document. Generating the XML’s for AUL, Rights & Roles and System Settings document. IVRS/IWRS- involving in IVRS (Integrated Voice response System) process from database

programming end. QCode Setup for Studies using Oracle Forms. Understand the importance of quality and deliver the task with high quality. Understand expectations of the customer and provided the quality on or before the time lines. Proactively plan things as per the project timelines and plan the work as per quality standards. Actively participated in the team meetings and study meetings and provide valuable inputs. Successfully implement the decisions taken in the team and study meetings. Understand the root cause of the problems and resolved the problems which involved fixes of

bug and ISEs. Successfully support the supportive change and innovations.

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Proactively communicated the things with the project team members and executed the planned deliverables.

Effectively communicated with the onshore team members and smoothly delivered the deliverables.

ACCENTURE SERVICE PVT. LTD., BANGALORESubject Matter Expert , (June 2008 till April 2011)

A competent professional with approx. 3 years of experience in various aspects of Design, Development, Implementation, Testing and User Support, contributing in various challenges in Health and Life Sciences. 

Projects Handled:Health & Life Science(Clinical Data Management)Duration: June 2008 till April 2011Role: Study Builder(CDS Developer) and Standards TeamPlatform: Windows XPLanguages / Tools: VB Scripting, CDM, Inform tool (4.5 and 4.6)

Job Profile:

Develop electronic clinical data management (eCDM) systems (eCRFs, edit checks, visit structures, system settings, role assignments, etc.)

Review specifications - to assure whether the requirements are clear and appropriate.

Understand, and apply Client standards library to each study build.

Maintain issues logs and seek issue resolutions to assure delivery on time

Perform peer review for studies built by team members and complete necessary documentation.

Conduct change and proper version control process for requested and approved changes to production studies.

Identify and Implements improved/innovative work processes or client/customer service

Mentor new study builders in their new roles, assist and provide guidance for successful delivery.

Perform Post-Production Changes (Revision without versioning) for the studies gone live.

Resolving Help desk cases raised by users for any problem occurred in Inform Trial and assigning tasks to team members.

Perform all tasks as required by SOPs.

Role and Responsibilities in Standards (Programmer)

Role: Standard Library Core 2.0 and Migraine Therapeutic area Tool or Application: Inform Tool

Job Profile:

Efficiently and effectively built the Core 2.0 Standards from scratch. Generated Codes and checks for Therapeutic area like Migraine, Neuro Sciences, Vaccines,

etc. Maintained the standards library to be used by all builders for forthcoming live projects.

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Report Development:Role: Report Developer

Tool or Application: SQL

Integrating Build and Reports Development: ICR,OICR,DRP developed at UAT1 package deployment for all studies.

Maintain appropriate documentation as required by SOPs. Perform all tasks as required by SOPs.

EDUCATION HISTORYMasters of Business Administration(MBA)

Symbiosis University, Pune(PGDMA) Completed the degree course with 78%

July 2013

Graduation (Bachelor of Bio-Technology)

Garden City College, Bangalore University, Bangalore, Karnataka

Completed the degree course with 87% Concentration: Biotechnology,Chemistry,Genetics

June 2008

Senior Secondary Examination St. Francis School, ICSE Board, Varanasi, Uttar Pradesh

Passed 12th Class with 84% Concentration: Physics, Chemistry, Biology

2005

Other Technical skills:

Operating systems : Windows 98/2000/XP/Vista/7.

Programming Languages : C, C++

Web Technologies : HTML,VB Scripting, cmd.

Database : SQL, Oracle Form Builder

Clinical Tools: Inform Architecture, Central Designer , Oracle Form Builder.

PROFESSIONAL QUALIFICATION AND CERTIFICATION

Diploma in Bio-Informatics, Euclaire Institute, US

Additional Information

Proficient in English & Hindi (R/W/S) Microsoft Office. Enthusiastic & attentive towards work. Inquisitive mind, good communication skills. Eager to learn makes me stand out of crowd.

Personal DetailsName: Priyanka Agarwal

Father’s Name: Late Sri Umesh Agarwal

Date of Birth: 27th August 1987

Nationality: Indian

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Marital Status: Single

Languages Known: English, Hindi

DECLARATION

I hereby declare that the above mentioned details are true to the best of my knowledge and belief

Date:

Place: Bangalore (Priyanka Agarwal)