Clinical Research, CDM, SAS programmer, Medical Coding Job openings for Bsc, B pharm, M pharm & Msc Candidates 2022
Cliantha Research Biometrics Department Job openings for Bsc, B pharm, M Pharm, Msc Candidates in CDM, Medical Coding, SAS programmer, Clinical Research Sections
Department : Biometrics
Designation : CDM
Basic qualification required : BSC / MSc / B Pharm / M Pharmacy
Experience : 2to 6 Years
Location : Ahmedabad
Job Description :
Create, maintain and update study specific documents like Data Management Plan, Creation of Data
Validation Plan, study specific procedures, data reconciliation plan and other study specific documents.
Designing Case Report Forms for paper and EDC studies and reviewing CRFs design.
Perform data entry in the database whenever required.
Co-ordinate with other study team members for data management related tasks on study activity.
Creating and Testing of UAT data in study database based on the edit checks created to maintain data integrity at the time of project deliverable.
Check consistency of Data Entry screens with case report form.
Train the clinical sites on using the study specific database for Electronic Data Capture (EDC) studies.
Identify and resolve data discrepancies in clinical data via computerized and manual data checks.
Perform the Quality Review of live data.
Apply level 1 correction to the database as and when required.
Generate queries, Update and Verify the received DCFs and Ex-DCFs.
Handle the external data and perform the applicable external data reconciliation process and resolve
queries pertaining to the external data.
Perform Serious Adverse Event (SAE) Reconciliation and resolve queries pertaining to the SAEs.
Perform Medical Coding of terms reported on Case Report Form.
Be compliant with Standard Operating Procedure, work procedures and project scope of the work and ensure quality.
Maintain documentation of training as appropriate.
Work with other members of the project team. This includes but is not limited to External team, Programmer, Statistician, Monitor and CRA.
Conforms to training schedule for self, maintains awareness of SOP content in the Data Management team, according to company requirements
Interested candidates can send their resume at [email protected]
Medical Coder – Biometrics
Designation : Medical Coder
Education : BSC / MSc / B Pharm / M Pharm
Job Description :
- Perform Medical Coding of terms reported on Case Report Form.
- Provide inputs on medical coding
- Perform medical coding UAT
- Provide technical expertise
- Work closely with the Dictionary authorities on the version upgrade and implementation.
- Maintain coding specific study documents.
- Liaise with the Study Lead on study deliverables.
- Provide trainings to new joiners in the team.
- Conduct refresher trainings.
- Be compliant with Standard Operating Procedure, work procedures and project scope of the work and ensure quality.
- Maintain documentation of training appropriate.
- Work with other members of the project team. This includes but is not limited to External team, Programmer, Statistician, Monitor and CRA.
- Conforms to training schedule for self, maintains awareness of SOP content in the Data Management team, according to company requirements.
Interested candidates can send their resume at [email protected]
Consumer Research
Designation : Officer / Sr. Officer
Basic Qualification Required : B Pharmacy / M Pharm / M Sc
Experience : 2 to 4 Years
Location : Ahmedabad
Job Description :
Identify and qualify potential investigators
Responsible for identification & collection of necessary documents in order to check the feasibility of site investigator and approval from authorities.
Responsible for training of site study team, recording & maintenance of essential documents and for startup
activities & site initiation.
Conduct of monitoring visits to check compliance with study management, protocol & other requirements at all
assigned sites.
Perform source document verification as per monitoring plan and ensure that source documents & other trial records are accurate, complete, kept up-to-date & maintained according to applicable SOP’s to avoid incomplete records.
Responsible for study updates & Coordination with Labs & other trial related services as per the study requirements.
Responsible for IP accountability and availability, tracking and management of all Clinical Trial related supplies shipped to the sites / warehouse & accordingly clinical trials supplies vendor management for the study.
Responsible for site-closeout & follow up activities in order to maintain documents at the site.
Assist with the audit of an investigational site or central files and liase with Quality Assurance personnel as required to ensure that the study is being conducted in accordance with ICH GCP and applicable regulatory guidelines
Interested candidates can send their resume at [email protected]
SAS Programmer – Biometrics
Designation : SAS Programmer
Education : BSC / B Pharm / MSc / MTech + SAS Certification
Experience : 02 to 06 years
Location : Mumbai / Ahmedabad
Job Description :
Generate safety and efficacy tables, listings and Figures for CT Projects
and standalone studies.
Validate programs and outputs of developers (if the candidate has 2+
years of experience).
Review Mock shells and CRF.
Communicate with cross functional team and sponsor if required for better clarity with outputs
Additional duties that are being allocated by the team lead.
Generate SDTM domains and AdaM datasets as required with respect to
allocation
Validate CDSIC datasets and programs of developers (if the candidate has
2+ years of experience).
Communicate with cross functional team and sponsor if required for better clarity with outputs
Preparing Annotated CRF.
Documentation: – ADRG, SDRG, Define.xml, Specification.
Resolving Pinnacle errors
Interested candidates can send their resume at [email protected]
Walk in Drive Details :
Date: 22nd January 2022 (Saturday) | Time: 10:00 AM to 5:00 PM
Location: Cliantha Research Limited, 7, Garden View, Opp. Auda Garden, Sindhu Bhavan Road, Bodakdev, Ahmedabad
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