Opportunity to work in Clinical Data Management Domain @ Manipal Acunova
Ecron Acunova provides end-to-end services for Phase I - IV clinical research, including Clinical Trial Management, Clinical Data Management, PK/PD services and Central Lab. Ecron Acunova has research facilities in Asia as well as an established presence in various parts of Europe and the United States. As regional experts, we operate each region as a priority market. Our European HQ is in Frankfurt, Germany, in the United States our HQ is in Princeton, NJ and our Asian HQ is in Bangalore, India. We offer clinical development services to the pharmaceutical, biotechnology, nutritional, device and medical diagnostics industries. Our service quality, therapeutic expertise and global reach have allowed us to grow rapidly, building a list of demanding clients.
Job Title: Clinical Data Management System (cdms)- Database Programmer
Qualification: B.tech/ M.sc Life science / Clinical research
Experience: 1-3 years
Job Description:
Database designing and programming of validation checks in compliance with the protocol, sponsor specifications and end user requirement with the maximum optimization for the data to be extracted at SAS level.
Database finalization from SAS extracts to prevent any amendment in the design later due to lack of understanding.
To participate and give input for process optimization in alignment with the SOW and sponsor's requirement with respect to the database designing process and project specific requirements.
Perform CRF Annotation of all the data points as per the standard document or as per sponsor requirement for a paper based study.
Programming of clinical database for data management projects.
Database designing, and validation in compliance with the study protocol and sponsor specifications and end-user requirement including TMS integration to the database.
How to apply:
Interested candidates can apply by sending their resume to careers-asia@ecronacunova.com
Ecron Acunova provides end-to-end services for Phase I - IV clinical research, including Clinical Trial Management, Clinical Data Management, PK/PD services and Central Lab. Ecron Acunova has research facilities in Asia as well as an established presence in various parts of Europe and the United States. As regional experts, we operate each region as a priority market. Our European HQ is in Frankfurt, Germany, in the United States our HQ is in Princeton, NJ and our Asian HQ is in Bangalore, India. We offer clinical development services to the pharmaceutical, biotechnology, nutritional, device and medical diagnostics industries. Our service quality, therapeutic expertise and global reach have allowed us to grow rapidly, building a list of demanding clients.
Job Title: Clinical Data Management System (cdms)- Database Programmer
Qualification: B.tech/ M.sc Life science / Clinical research
Experience: 1-3 years
Job Description:
Database designing and programming of validation checks in compliance with the protocol, sponsor specifications and end user requirement with the maximum optimization for the data to be extracted at SAS level.
Database finalization from SAS extracts to prevent any amendment in the design later due to lack of understanding.
To participate and give input for process optimization in alignment with the SOW and sponsor's requirement with respect to the database designing process and project specific requirements.
Perform CRF Annotation of all the data points as per the standard document or as per sponsor requirement for a paper based study.
Programming of clinical database for data management projects.
Database designing, and validation in compliance with the study protocol and sponsor specifications and end-user requirement including TMS integration to the database.
How to apply:
Interested candidates can apply by sending their resume to careers-asia@ecronacunova.com
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