Hope you are doing great,
Please let me know if you have any good resources for the below position mentioned
Role : Sr. Clinical Data Analyst
Duration : 12 + months
Location : Montvale, NJ
Candidates should be local for a face to face interview. Skype is NOT an option.
Strong experience in programming complex MACROS is a must. Experience with JReview/IReview. Good knowledge of CDISC, SDTM, MedDRA, and WHODRUG. Please let me know if you have any candidates.
Responsibilities:
Perform SAS programming to provide data review complex listings/reports to support Data Management function Oncology trials.
Provide patient profiles and complex reports for data review to support the clinical teams for data review and data cleaning.
Assist in preparing datasets for statistical analysis and regulatory submissions
Participate in review process of study documents such as the annotated CRFs/eCRFs, edit check specification.
Program data edit checks as necessary to facilitate Data Management's data cleaning activities.
Design and develop complex SAS macros, applications, and other utilities to expedite SAS programming activities and usage by the Oncology
Data Management and other areas of Clinical for data review.
Develop and maintain the programs including testing and organizing the SAS datasets, SAS programs and related documentation.
Ensure all programming activities and processes performed are conducted according to standard operating procedures and good
programming skills.
Qualifications:
Strong SAS programming skills required in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph,
SAS/AF/SQL.
7-10 years of experience in programming with clinical trial data and preparing programming and test documentation.
Extensive experience of handling external data, such as lab data, PK and of using JReview/IReview.
Good understanding of standards specific to clinical trials such as CDISC, SDTM, MedDRA, WHODRUG.
Good understanding of relational databases such as ORACLE, Understanding/experience with SAS based application development,
Knowledge of the EDC system, InForm, and underlying data structure is a plus.
Knowledge of data management process, good understanding of data cleaning process.
Strong problem solving skills
Able to work independently and a team player, good organizational and time management skills.
Capable of communicating technical concepts
Good understanding of system development life cycles, GCP, and related regulatory guidelines.
*Strong experience in programming complex macros, reports, and patient profiles
Bhavika
Rider Consulting Inc.
Email : Bhavika@riderconsultinginc.com
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