Cdm Programmer Ii

Summarized Purpose: Works with clinical data management systems and programming tools to provide advanced programming support in data management activities and deliverables including, but not limited to, database development and data validations, and assisting with defining tools and techniques for improving process efficiencies. Works within a...

Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading global...

Summarized Purpose:Works with clinical data management systems and programming tools to provide advanced programming support in data management activities and deliverables including, but not limited to, database development and data validations, and assisting with defining tools and techniques for improving process efficiencies. Works within a...

**Job Title: Clinical Programmer II** **Career Level - C2** **Introduction to Role**: Join our Oncology R&D team as a Clinical Programmer II, where you will primarily be responsible for supporting activities related to programming, dashboard development, and validation of data cleaning and review listings for ongoing clinical studies with Medium to High...

Job Title: Clinical Programmer IICareer Level - C2Introduction to Role:Join our Oncology R&D team as a Clinical Programmer II, where you will primarily be responsible for supporting activities related to programming, dashboard development, and validation of data cleaning and review listings for ongoing clinical studies with Medium to High Complexity. This...

**Brief Position Description**: The Clinical Data Programmer SAS is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating reports,...

Brief Position Description: Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements, and Novotech/Client SOPs. Minimum Qualifications & Experience: Graduate in a clinical or life sciences related...

**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...

JOB DESCRIPTION:Job Qualification:Diversity Statement: PPD is proud to be an affirmative action employer that values diversity as a strength and fosters an environment of mutual respect. PPD is committed to providing equal employment opportunities without regard to age, race, color, pregnancy, national origin, religion, sex, gender identity, sexual...

Brief Position Description:Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements, and Novotech/Client SOPs.Minimum Qualifications & Experience:Graduate in a clinical or life sciences related field....

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and...

**Organization Description** Novotech is a leading Asia-Pacific biotech specialist CRO and consists of two operating brands, Novotech and PPC. Novotech is a clinical CRO with labs, phase I facilities, and drug development consulting services. It has accumulated experience in over 3,700 clinical projects, including Phase I to Phase IV clinical trials and...

**About the role**: The Clinical Data Programmer SAS III is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating reports, visualizations,...

**About the role**: The Clinical Data Programmer SAS III is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating reports, visualizations,...

**About the role**: The Clinical Data Programmer SAS III (must be SAS Certified) is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating...

Job Title: Senior Statistical Programmer II Career Level - D Introduction to Role: Are you a goal-oriented Statistical Programmer looking for a new challenge? Would you like to be a part of a group with direct strategic impact on drug development that plays a key role in getting new medicines to patients who need them? Welcome to join AstraZeneca...

Principal Duties ResponsibilitiesPerform and implement, under supervision,the following for clinical studies: (i) the SAS programming, testing, anddocumentation of statistical programs for use in creating statisticaltables, figures, listings, and graphs and (ii) the programming of analysisdatasets (derived datasets) and transfer filesfor internal and...

Principal Duties & ResponsibilitiesPerform and implement, under supervision, the following for clinical studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and...

**Principal Duties & Responsibilities** - Perform and implement, under supervision, the following for clinical studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files for...

Principal Duties & Responsibilities Perform and implement, under supervision, the following for clinical studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files for...