The Senior Manager in Statistics responsible for perform statistical activities in clinical trials ... guidelines, CDISC data structures and FDA guidelines Excellent organizational skills, time ...
Quick apply
The Senior Manager in Statistics responsible for perform statistical activities in clinical trials ... guidelines, CDISC data structures and FDA guidelines Excellent organizational skills, time ...
Senior Manager, Scientific Programming
Manhattan, NY · On-site
$144K - $189K/yr
Contribute to departmental process and standards initiatives such as tools and CDISC standards. Collaborate and support selection and management of CROs, including strategic outsourcing providers.
Senior Manager, Scientific Programming
Manhattan, NY · On-site
$144K - $189K/yr
Contribute to departmental process and standards initiatives such as tools and CDISC standards. Collaborate and support selection and management of CROs, including strategic outsourcing providers.
The Senior Manager in Statistics responsible for perform statistical activities in clinical trials ... guidelines, CDISC data structures and FDA guidelines Excellent organizational skills, time ...
The Senior Manager in Statistics responsible for perform statistical activities in clinical trials ... guidelines, CDISC data structures and FDA guidelines Excellent organizational skills, time ...
The role focuses on defining data flows, metadata, and CDISC implementation while advising on ... Ensure Data Management considerations are incorporated into validation, access controls, audit ...
The role focuses on defining data flows, metadata, and CDISC implementation while advising on ... Ensure Data Management considerations are incorporated into validation, access controls, audit ...
Clinical Data Manager
Austin, TX · On-site
Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). Manage database lock activities and contribute to the preparation of clinical study reports ...
Clinical Data Manager
Austin, TX · On-site
Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). Manage database lock activities and contribute to the preparation of clinical study reports ...
Responsible for biostatistical design, analysis, and reporting for regulatory submissions, using SAS and CDISC standards; manages vendors and performs hands-on statistical analyses to support product ...
Responsible for biostatistical design, analysis, and reporting for regulatory submissions, using SAS and CDISC standards; manages vendors and performs hands-on statistical analyses to support product ...
Senior Manager, Scientific Programming
$144K - $189K/yr
Contribute to departmental process and standards initiatives such as tools and CDISC standards. * Collaborate and support the selection and management of CROs (including the strategic outsourcing ...
Senior Manager, Scientific Programming
$144K - $189K/yr
Contribute to departmental process and standards initiatives such as tools and CDISC standards. * Collaborate and support the selection and management of CROs (including the strategic outsourcing ...
Responsible for biostatistical design, analysis, and reporting for regulatory submissions, using SAS and CDISC standards; manages vendors and performs hands-on statistical analyses to support product ...
Responsible for biostatistical design, analysis, and reporting for regulatory submissions, using SAS and CDISC standards; manages vendors and performs hands-on statistical analyses to support product ...
Data management support includes performing clinical data management activities or providing ... Develop SDTM datasets conforming to CDISC standards; Develop Analysis Data Model datasets ...
Quick apply
Data management support includes performing clinical data management activities or providing ... Develop SDTM datasets conforming to CDISC standards; Develop Analysis Data Model datasets ...
Senior Manager, Clinical Programming
Princeton, NJ · On-site +1
$131K - $196K/yr
... CDISC standards and other industry standards that supports the exchange of data, reporting, and ... management and related tools/applications • Creates quality control processes, metrics and other ...
Senior Manager, Clinical Programming
Princeton, NJ · On-site +1
$131K - $196K/yr
... CDISC standards and other industry standards that supports the exchange of data, reporting, and ... management and related tools/applications • Creates quality control processes, metrics and other ...
Data management support includes performing clinical data management activities or providing ... Develop SDTM datasets conforming to CDISC standards; Develop Analysis Data Model datasets ...
Data management support includes performing clinical data management activities or providing ... Develop SDTM datasets conforming to CDISC standards; Develop Analysis Data Model datasets ...
A leading global healthcare company is seeking an experienced Clinical Data Manager/Clinical Data ... experience in a pharmaceutical environment, proficient in CDISC standards, and excels in ...
A leading global healthcare company is seeking an experienced Clinical Data Manager/Clinical Data ... experience in a pharmaceutical environment, proficient in CDISC standards, and excels in ...
Data management support includes performing clinical data management activities or providing ... Develop SDTM datasets conforming to CDISC standards; Develop Analysis Data Model datasets ...
Data management support includes performing clinical data management activities or providing ... Develop SDTM datasets conforming to CDISC standards; Develop Analysis Data Model datasets ...
SAS Programmer
Falls Church, VA · On-site
... CDISC-compliant datasets (SDTM and ADaM) • Validate and document programming outputs • Collaborate with statisticians and data management teams • Support regulatory submissions and audits ...
Quick apply
SAS Programmer
Falls Church, VA · On-site
... CDISC-compliant datasets (SDTM and ADaM) • Validate and document programming outputs • Collaborate with statisticians and data management teams • Support regulatory submissions and audits ...
... management, technical oversight, and quality of statistical programming activities related to the analyses of clinical trial data ensuring timelines and company strategic objectives are met. A CDISC ...
... management, technical oversight, and quality of statistical programming activities related to the analyses of clinical trial data ensuring timelines and company strategic objectives are met. A CDISC ...
... management, technical oversight, and quality of statistical programming activities related to the analyses of clinical trial data ensuring timelines and company strategic objectives are met. A CDISC ...
... management, technical oversight, and quality of statistical programming activities related to the analyses of clinical trial data ensuring timelines and company strategic objectives are met. A CDISC ...
The Biostatistician will develop FDA-ready, CDISC-compliant deliverables, execute analyses per the ... Ability to work independently, manage shifting priorities, and deliver high-quality work on ...
The Biostatistician will develop FDA-ready, CDISC-compliant deliverables, execute analyses per the ... Ability to work independently, manage shifting priorities, and deliver high-quality work on ...
SAS Programmer
Falls Church, VA · On-site +1
... CDISC-compliant datasets (SDTM and ADaM) Validate and document programming outputs Collaborate with statisticians and data management teams Support regulatory submissions and audits Minimum ...
SAS Programmer
Falls Church, VA · On-site +1
... CDISC-compliant datasets (SDTM and ADaM) Validate and document programming outputs Collaborate with statisticians and data management teams Support regulatory submissions and audits Minimum ...
Data Management Consultant - Statistical Computing Environment Anywhere Type: Contract Category ... The role focuses on defining data flows, metadata, and CDISC implementation while advising on ...
Data Management Consultant - Statistical Computing Environment Anywhere Type: Contract Category ... The role focuses on defining data flows, metadata, and CDISC implementation while advising on ...
SAS Programmer
Falls Church, VA · On-site
... CDISC-compliant datasets (SDTM and ADaM) • Validate and document programming outputs • Collaborate with statisticians and data management teams • Support regulatory submissions and audits ...
SAS Programmer
Falls Church, VA · On-site
... CDISC-compliant datasets (SDTM and ADaM) • Validate and document programming outputs • Collaborate with statisticians and data management teams • Support regulatory submissions and audits ...
Manager Cdisc information
See salary details
$23K - $30.2K
4% of jobs
$30.2K - $37.5K
10% of jobs
$43.3K is the 25th percentile. Wages below this are outliers.
$37.5K - $44.7K
14% of jobs
$44.7K - $51.9K
16% of jobs
The median wage is $58.1K / yr.
$51.9K - $59.1K
7% of jobs
$59.1K - $66.4K
10% of jobs
$70K is the 75th percentile. Wages above this are outliers.
$66.4K - $73.6K
29% of jobs
$73.6K - $80.8K
4% of jobs
$80.8K - $88K
3% of jobs
$88K - $95.3K
1% of jobs
$95.3K - $102.5K
2% of jobs
$23K
$61.4K
$102.5K
How much do manager cdisc jobs pay per year?
As of Jun 5, 2026, the average yearly pay for manager cdisc in the United States is $61,351.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $69,000.00 per year, depending on experience, location, and employer.
What is the difference between Manager Cdisc vs Clinical Data Manager?
| Aspect | Manager Cdisc | Clinical Data Manager |
|---|---|---|
| Certifications | CDISC certifications, project management certifications | CDISC certifications, clinical data management certifications |
| Work Environment | Pharmaceutical or biotech companies, CROs | Pharmaceutical companies, CROs, research institutions |
| Responsibilities | Oversees CDISC standards implementation, manages data standards projects | Manages clinical data collection, validation, and database lock processes |
Both roles require knowledge of CDISC standards and data management. The Manager Cdisc focuses on overseeing standards implementation and project management, while the Clinical Data Manager handles day-to-day data collection and validation tasks. They often work together but have distinct responsibilities within clinical research teams.
More about Manager Cdisc jobs
What cities are hiring for Manager Cdisc jobs? Cities with the most Manager Cdisc job openings:
What are the most commonly searched types of Cdisc jobs? The most popular types of Cdisc jobs are:
What states have the most Manager Cdisc jobs? States with the most job openings for Manager Cdisc jobs include:
What job categories do people searching Manager Cdisc jobs look for? The top searched job categories for Manager Cdisc jobs are:
- Statistics Programmer
- Manager Statistical Programming
- Part Time Director Statistical Programming
- Sr Statistical Programmer
- Senior Manager Statistical Programming
- Senior Director Statistical Programming
- Director Statistical Programming
- Larimar Therapeutics
- Full Time Director Statistical Programming
- Statistical Programming
$72/hr
Contractor
Posted 28 days ago
Job description
JOB DESCRIPTION:
The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing.
RESPONSIBILITIES:
Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc.
Review CRF, database design, and edit check specs
Review study quality surveillance plan and monitor study conduct
Prepare and/or review SAP, TFL shells and specifications for variable derivation
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables
Provide statistical and validation support for statistical analysis, analysis datasets and TFL Review study report, manuscripts and other documents related to statistics
Work on responses to health authorities and execute new analysis required for responses, review statistical inputs for regulatory documents
Perform other ad-hoc statistical activities as needed
Works effectively with cross functional groups, study team, and vendors. Proactively control and monitor timelines related to statistics and statistical programming
Participates in monitoring CRO activities and reviewing CRO deliverables
Other duties as assigned
Review CRF, database design, and edit check specs
Review study quality surveillance plan and monitor study conduct
Prepare and/or review SAP, TFL shells and specifications for variable derivation
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables
Provide statistical and validation support for statistical analysis, analysis datasets and TFL Review study report, manuscripts and other documents related to statistics
Work on responses to health authorities and execute new analysis required for responses, review statistical inputs for regulatory documents
Perform other ad-hoc statistical activities as needed
Works effectively with cross functional groups, study team, and vendors. Proactively control and monitor timelines related to statistics and statistical programming
Participates in monitoring CRO activities and reviewing CRO deliverables
Other duties as assigned
QUALIFICATIONS:
Education: Ph.D. or MS in Statistics or Biostatistics
Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience
Excellent knowledge of SAS computer package
Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines
Excellent organizational skills, time management, and ability to meet established deadlines.
Excellent communication and interpersonal skills to effectively interface with others
Exceptional interpersonal skills and problem-solving capabilities
Ability to work independently and collaboratively
Ability to provide leadership for the CRO statisticians and statistical programmers
Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience
Excellent knowledge of SAS computer package
Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines
Excellent organizational skills, time management, and ability to meet established deadlines.
Excellent communication and interpersonal skills to effectively interface with others
Exceptional interpersonal skills and problem-solving capabilities
Ability to work independently and collaboratively
Ability to provide leadership for the CRO statisticians and statistical programmers
PHYSICAL AND MENTAL REQUIREMENTS:
Ability to multitask
Adapts to change
Maintain composure under pressure
Ability to follow verbal or written instructions and use of effective verbal communications
Adapts change, adjust change and grasps information quickly
Examine and observe details
Adapts to change
Maintain composure under pressure
Ability to follow verbal or written instructions and use of effective verbal communications
Adapts change, adjust change and grasps information quickly
Examine and observe details
About Talentsearchpro
Sourced by ZipRecruiter
Industry
Human resources consulting services
Company size
1 - 10 Employees
Headquarters location
Oakland, CA, US