Reporting to the EMR Manager, the Senior Programmer Analyst/Clinical Data Analyst will collect and aggregate data from various providers and be responsible for the translation and interpretation of op...

Reporting to the EMR Manager, the Senior Programmer Analyst/Clinical Data Analyst will collect and aggregate data from various providers and be responsible for the translation and interpretation of op...

Create and maintain department SOPs related to clinical programming. Minimum of 5 years of experience in developing software for clinical trials using the SAS system. Experience as a lead programmer f...

Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...

Design and specify study data tabulation models and analysis data models for clinical trials or for the integration of clinical trial data from multiple trials (e. Everest Clinical Research ("Everest"...

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...

Good knowledge of pharmaceutical clinical development (, understanding of statistical concepts, techniques, and clinical trial principles). Ensures accurate programming of SAS clinical data extracts a...

Good knowledge of pharmaceutical clinical development (, understanding of statistical concepts, techniques, and clinical trial principles). Experience: At least years of SAS programming experience wit...

Create and QC statistical outputs and clinical study reports for regulatory submissions. Work closely with biostatisticians, data managers, and clinical researchers. Develop and maintain SAS programs ...

Create and QC statistical outputs and clinical study reports for regulatory submissions. Work closely with biostatisticians, data managers, and clinical researchers. Develop and maintain SAS programs ...

POST MARKETING-PRECLINICAL-PHASE OR LATER.

POST MARKETING-PRECLINICAL-PHASE OR LATER.

Experience with different clinical phases. Knowledge of clinical trial methodology and study design. TLF) shells, SDTM/ADaM specifications, clinical study reports, and other relevant documents.

TLF) shells, SDTM/ADaM specifications, clinical study reports, and other relevant documents. Experience with different clinical phases. Knowledge of clinical trial methodology and study design.

Good to have experience with ECS (eClinical Solution) ETL tool. ETL tools such as Informatica, Data Stage or eClinical Solutions. Clinical is the preferred tool.

Good to have experience with ECS (eClinical Solution) ETL tool. ETL tools such as Informatica, Data Stage or eClinical Solutions. Clinical is the preferred tool.

This position will be dedicated to the Clinical Data Warehousing & Delivery function within the Clinical Data Reporting & Analytics group and contribute to the improvement of clinical data review, cle...

This position will be dedicated to the Clinical Data Warehousing & Delivery function within the Clinical Data Reporting & Analytics group and contribute to the improvement of clinical data review, cle...

Minimum - years in a clinical programming role. Represent the Clinical Programming function at cross-functional meetings.

Minimum - years in a clinical programming role. Represent the Clinical Programming function at cross-functional meetings.

Familiarity with clinical trial data and CDISC standards.

Familiarity with clinical trial data and CDISC standards.

Working understanding of clinical trial principles and technical implications. Working knowledge of clinical development. Ability to ensure clinical database programming work is completed in a consist...

Designs and creates clinical databases to enable data review/validation of the study data by Data Managers, and a comprehensive and efficient analysis by Statistics and SAS Programming. Establishes an...

Join our Clinical Data Reporting & Analytics team as a Clinical Programmer. Job Title: Clinical Programmer. You'll be a key player in improving clinical data review and statistical analyses by providi...

Join our Clinical Data Reporting & Analytics team as a Clinical Programmer. Job Title: Clinical Programmer. You'll be a key player in improving clinical data review and statistical analyses by providi...

This position will be dedicated to the Clinical Data Warehousing & Delivery function within the Clinical Data Reporting & Analytics group and contribute to the improvement of clinical data review, cle...

This position will be dedicated to the Clinical Data Warehousing & Delivery function within the Clinical Data Reporting & Analytics group and contribute to the improvement of clinical data review, cle...

The Senior Clinical Database Programmer is responsible for ensuring that clinical study data is collected, processed, and validated in a consistent and appropriate manner that is consistent with BD’s ...

The Senior Clinical Database Programmer is responsible for ensuring that clinical study data is collected, processed, and validated in a consistent and appropriate manner that is consistent with BD’s ...

Demonstrate knowledge of real-world evidence (RWE) databases and clinical trial data. Apply various statistical methods to real-world research and clinical trial studies.

Demonstrate knowledge of real-world evidence (RWE) databases and clinical trial data. Apply various statistical methods to real-world research and clinical trial studies.

SAS Programmer will be responsible for leveraging their extensive experience and expertise to lead the development, implementation, and validation of SDTM (Study Data Tabulation Model) datasets for cl...

Designs and creates clinical databases. Minimum years clinical database programming experience preferred in the device / pharmaceutical / CRO industry. Experience with development, validation, executi...

SAS Programmer will be responsible for leveraging their extensive experience and expertise to lead the development, implementation, and validation of SDTM (Study Data Tabulation Model) datasets for cl...

Industry experience as a clinical trial SAS programmer; SAS experience in drug development in CRO or pharma/biotech company. Our client, a global pharmaceutical organization, has engaged GForce Life S...

Our client, a global pharmaceutical organization, has engaged GForce Life Sciences to provide them with a Clinical Programmer. This SAS programmer will support an ongoing and planned 2022 clinical tri...