Sr Clinical Data Analyst REMOTE
Posted on :
12-06-2024
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Job Description
For further inquiries regarding the following opportunity please contact one of our Talent Specialists
Meghna at
Rashi at
Meghna at
Rashi at
Title: Sr Clinical Data Analyst (REMOTE)
Location: Remote
Duration: 6 Months
Location: Remote
Duration: 6 Months
Description:
Day to Day Responsibilities:
Designs clinical trial specific subject Case Report Forms for use in eclinical EDC systems.
Develops study specific annotated CRFs database documentation edit check specifications data handling conventions and data entry instructions.
Designs and validates clinical databases including designing logic checks UAT etc.
Knowledge of MedDRA and WHODrug Coding.
Programs SAS edit checks and SAS macros for data cleaning.
Processes clinical data including receipt entry verification and filing of information.
Generates data queries based on validation checks or errors or omissions identified during data entry to resolve identified problems.
Performs quality control audits to ensure accuracy completeness and proper use of clinical data system.
Responsible for filing and maintaining CRFs subject diaries and other subjectspecific documentation (e.g. Marketing questionnaires) collected during clinical studies.
Responsible for filing and maintaining digital data collected during clinical studies.
Summarizes basic elements for clinical databases periodically.
Communicates with end users to define or implement clinical data management requirement for the clinical study such as data release delivery schedules and testing protocols.
Provides training and technical support to clinical site personnel on EDC for specific studies.
Maintains more than 3 study databases and data management activities concurrently.
Ability to multitask while still being detail oriented.
Develops projectspecific data management plans that address areas such as data reporting transfer database lock and work flow.
Monitors work quality to ensure compliance with standard operating procedures.
Day to Day Responsibilities:
Designs clinical trial specific subject Case Report Forms for use in eclinical EDC systems.
Develops study specific annotated CRFs database documentation edit check specifications data handling conventions and data entry instructions.
Designs and validates clinical databases including designing logic checks UAT etc.
Knowledge of MedDRA and WHODrug Coding.
Programs SAS edit checks and SAS macros for data cleaning.
Processes clinical data including receipt entry verification and filing of information.
Generates data queries based on validation checks or errors or omissions identified during data entry to resolve identified problems.
Performs quality control audits to ensure accuracy completeness and proper use of clinical data system.
Responsible for filing and maintaining CRFs subject diaries and other subjectspecific documentation (e.g. Marketing questionnaires) collected during clinical studies.
Responsible for filing and maintaining digital data collected during clinical studies.
Summarizes basic elements for clinical databases periodically.
Communicates with end users to define or implement clinical data management requirement for the clinical study such as data release delivery schedules and testing protocols.
Provides training and technical support to clinical site personnel on EDC for specific studies.
Maintains more than 3 study databases and data management activities concurrently.
Ability to multitask while still being detail oriented.
Develops projectspecific data management plans that address areas such as data reporting transfer database lock and work flow.
Monitors work quality to ensure compliance with standard operating procedures.
Required Skills (top 3 nonnegotiables):
1. Develops study specific CRF
2. Programs SAS edit checks and SAS macros
3. Designs and validates clinical databases
1. Develops study specific CRF
2. Programs SAS edit checks and SAS macros
3. Designs and validates clinical databases
Preferred Skills (nice to have)
1. Power BI
2. Medical coding
3. Data management documentation
1. Power BI
2. Medical coding
3. Data management documentation
Education Requirements: Bachelors degree in a technical discipline and a minimum of 58 years related experience or Masters degree and 25 years equivalent industry experience or a PhD and 02 years experience.
Software Skills Required: SAS SQL
Required Certifications**: SAS base certification
About us: DivIHN the IT Asset Performance Services organization provides Professional Consulting Custom Projects and Professional Resource Augmentation services to clients in the MidWest and beyond. The strategic characteristics of the organization are Standardization Specialization and Collaboration. DivIHN is an equal opportunity employer. DivIHN does not and shall not discriminate against any employee or qualified applicant on the basis of race color religion (creed) gender gender expression age national origin (ancestry) disability marital status sexual orientation or military status.
Employment Type
Full Time
Key Skills
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