Molla Mohammed Iqlas

Mobile: 910*******

E-Mail: adnz2p@r.postjobfree.com

Profile Snapshot

Worked with HCL Technologies Limited, Chennai, India from 2020 Mar 11th to till date as Software Engineer.

Clinical SAS Programmer with over 1 years and 4 months of experience in mapping, designing and validating the applications regarding clinical trials

Good programming experience with Base SAS, SAS Macro Language and Procedures.

Knowledge in Phase I to Phase IV Clinical Trails as per SDTM 3.2 guidelines

Good experience on SAS working in UNIX environment.

Expertise in CDISC SDTM Mapping & In-depth knowledge of Clinical data & CDISC SDTM Implementation Guides.

Expertise in programming of Domains like Demographic Data, Adverse Events (AE), DISPOSITION (DS Data), Exposure data(EX) etc. by following aCRF, SDTM Mapping Specifications.

Experience on various SAS procedures like Proc format, Proc sql, Proc means, Proc Freq, Proc Report,

Proc Transpose, Proc Compare etc.

Basic understanding in ADaM.

Education

Bachelor of Technology from Jawaharlal Nehru Technological University in Anantapur.

Personal Details

Date of Birth : 08 Mar 1998.

Languages : English, Hindi, Telugu.

Address : Kurnool, India.

Clinical SAS Skills

Identifying the standard and protocol specific SDTM domains based upon CRF data.

Good Knowledge on SDTM implementation guide.

Good Experience on Creating the CRF annotations and reviewing the SDTM datasets.

Good programming skills for SDTM mapping solutions as per requirements.

Base SAS Skills

SAS Base, SAS Macros, SAS/STAT, SAS SQL, Clinical SAS.

SAS Functions, Operators, Statements and procedures.

SAS Procedures such as Proc print, Proc SQL, Proc sort, Proc format, Proc transpose, Proc Import, Proc export.

Reporting Procedures: Proc Means, Proc Freq, Proc Transpose and Proc Summary.

Responsibilities/ Key Highlights: (Project 1 – SDTM/SAS Programming)

Good understanding of Clinical Development and Operational process and regulatory requirements.

Identify the required SDTM domains by reviewing documents like Specifications, eCRF and create SDTM project plan for study.

Developing SDTM annotated CRF and specifications

Develop and Validate SDTM domains as per SDTM IG/Sponsor standards.

Responsibilities/ Key Highlights: (Project 2 – SDTM/SAS Programming)

Participate in Kick Off meeting, read and understand thoroughly about study documents like Protocol and CRF.

eCRF annotation using standards and suggest mapping for non-standard variable or SDTM domain.

Develop Programs using CRF/SAS

CRF annotation, SDTM dataset development and QC

Maintain Controlled Terminology as per SDTM standards

Declaration

I hereby declare that all the statements mentioned above are true to my knowledge and belief.

Place: Chennai

Date:

Contact this candidate