Clinical Data Programmer (Oncology)
To see similar active jobs please follow this link: Remote Development jobs
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….
ClinChoice is searching for a Clinical Programmer Consultant to join one of our clients.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
Summary
The primary responsibility of the Clinical Data Programmer Consultant will be to program data review listings and reports for assigned studies and provide other clinical programming support as needed. This role must effectively interface with Data Management and other cross-functional areas involved in clinical data review using SAS.
Main Job Tasks and Responsibilities:
Programs SAS Non-System Edit Checks, Protocol Deviations, and SAS Data Listings
Ability to independently develop innovative and complex SAS programs to support activities including, but not limited to, data review and reporting
Supports the maintenance of the Non-System Edit Check Global Library to ensure consistency across programs and studies and concordance with the EDC Global Library
Create SAS program Specifications for Non-System Edit Checks based on CRF and non-CRF data.
Responsible for participating in the development and review of data transfer specifications, processing of clinical data downloads, and data transfers to/from service providers
Create Clinical Data Review Tools [i.e., Data Listing Reports (DLRs); External Data Reconciliation Listings, Medical Safety Listings for reconciliation, etc.] for all studies based on study-specific specs and requirements.
Supports the development, delivery, and maintenance of clinical data review standards, tools, and systems, across various data sources (e.g., clinical data, safety, and operational data).
Supports initiatives for Data Management, Clinical Programming, Clinical Data Science, and/or Safety/Clinical Data Review bridging activities, meetings, and discussions.
Works with cross-functional team members to develop new or improve existing data review tools
Education and Experience:
Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 7-8 yrs. Master’s degree in CS, statistics, or related disciplines with 7+ yrs.
Require strong Oncology TA experience.
Excellent programming skills including SAS & R language.
The Application Process
Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
#LI-TT1 #LI-Remote #Senior #Contract
About the job
Clinical Data Programmer (Oncology)
To see similar active jobs please follow this link: Remote Development jobs
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….
ClinChoice is searching for a Clinical Programmer Consultant to join one of our clients.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
Summary
The primary responsibility of the Clinical Data Programmer Consultant will be to program data review listings and reports for assigned studies and provide other clinical programming support as needed. This role must effectively interface with Data Management and other cross-functional areas involved in clinical data review using SAS.
Main Job Tasks and Responsibilities:
Programs SAS Non-System Edit Checks, Protocol Deviations, and SAS Data Listings
Ability to independently develop innovative and complex SAS programs to support activities including, but not limited to, data review and reporting
Supports the maintenance of the Non-System Edit Check Global Library to ensure consistency across programs and studies and concordance with the EDC Global Library
Create SAS program Specifications for Non-System Edit Checks based on CRF and non-CRF data.
Responsible for participating in the development and review of data transfer specifications, processing of clinical data downloads, and data transfers to/from service providers
Create Clinical Data Review Tools [i.e., Data Listing Reports (DLRs); External Data Reconciliation Listings, Medical Safety Listings for reconciliation, etc.] for all studies based on study-specific specs and requirements.
Supports the development, delivery, and maintenance of clinical data review standards, tools, and systems, across various data sources (e.g., clinical data, safety, and operational data).
Supports initiatives for Data Management, Clinical Programming, Clinical Data Science, and/or Safety/Clinical Data Review bridging activities, meetings, and discussions.
Works with cross-functional team members to develop new or improve existing data review tools
Education and Experience:
Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 7-8 yrs. Master’s degree in CS, statistics, or related disciplines with 7+ yrs.
Require strong Oncology TA experience.
Excellent programming skills including SAS & R language.
The Application Process
Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
#LI-TT1 #LI-Remote #Senior #Contract