Clinical Data Programmer, Oncology (Contract) - JOB ID: JEHO
DescriptionHere at Ascendis we pride ourselves in exceptional science, visionary leadership, skilled and passionate colleagues.
We are a dynamic, fast-growing biopharma company with offices in Denmark, Germany, and the United States.
Today, we re advancing programs in Endocrinology Rare Disease, and Oncology.
Guided by our core values of patients, science, and passion, we use our TransCon drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.
Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark.
We are a dynamic workplace for employees to grow and develop their skills.
The Clinical Data Programmer will be responsible for performing SAS programming (SAS/SQL program and macro validation, data and programming quality checks, validation document generation) to support data management/clinical development operational activities.
This includes developing customized, programmed data listings and data reports/visualizations to support clinical data review and process efficiency.
The Clinical Programmer will lead clinical programming activities across one or more studies.
This role reports to Senior Director, Data Management, Oncology.
Key ResponsibilitiesCreates standard and/or custom programs/reports using data analytics tools such as SAS, Tableau, or other data visualization tools to support data oversight and review by data managers or other data reviewers.
Collaborates with Data Management, Clinical Development, Clinical Operations, Drug Safety, Statistical Programming, and Biostatistics to develop standard and custom data reports for quality data oversight / clinical data review.
Generates safety surveillance and/or safety quality data review outputs and patient profiles for Drug Safety and Clinical Development clinical data review.
Provides leadership, training, guidance, and support to other department members on data review tools such as SAS.
Collaborates with clients, peers, programmers, project teams, and/or requestors to clarify and finalize data specifications; uses expanded technical skills to meet evolving project needs.
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 and Clinical Programming for clinical data review bridging activities, meetings, discussions.
Possesses and maintains a broad overall knowledge in the field of clinical programming and clinical data management by reading related literature, self-training, attending training classes, attending professional meetings, etc.
RequirementsBachelor s degree (or equivalent) in Science and/or Computer Systems/IT backgroundMinimum 4 years experience in a pharmaceutical/biotech settingAdvanced programming and analytical skills using BASE/SAS, SAS/STAT, SAS MACROSStrong knowledge of Oncology clinical trialsData Visualization tools (like Tableau, Spotfire) and Python programming language experience a plusAbility to work independently to create standard datasets, program edit checks and produce quality data review outputsGeneral knowledge of industry standards and best practices such as CDISC/CDASH, SDTM, data standardization.
(FHIR and OMOP a plus)Windows applications:
Word, Excel, PowerPoint, etc.
Excellent analytical, problem-solving, organizational, time-management, interpersonal and communication skills Comfortable developing and debugging programs independently and without supervisionGood written and oral presentation skills and ability to communicate effectively to other programmers and non-technical colleaguesAbility to think creatively and independently, and to form sound opinions and make sensible decisions in a dynamic environmentThis position may be considered for remote only workThis is a contract position, estimated length of assignment - 6 monthsSalary range:
$60-$75/hr DOEA note to recruiters:
We do not allow external search party solicitation.
Presentation of candidates without written permission from the Ascendis Pharma Inc Human Resources team (specifically from:
Talent Acquisition Partner or Human Resources Director) is not allowed.
If this occurs your ownership of these candidates will not be acknowledged.
Job SummaryID:
8E52BE91EEDepartment:
Oncology, Clinical Operations, Oncology.
Estimated Salary: $20 to $28 per hour based on qualifications.
We are a dynamic, fast-growing biopharma company with offices in Denmark, Germany, and the United States.
Today, we re advancing programs in Endocrinology Rare Disease, and Oncology.
Guided by our core values of patients, science, and passion, we use our TransCon drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.
Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark.
We are a dynamic workplace for employees to grow and develop their skills.
The Clinical Data Programmer will be responsible for performing SAS programming (SAS/SQL program and macro validation, data and programming quality checks, validation document generation) to support data management/clinical development operational activities.
This includes developing customized, programmed data listings and data reports/visualizations to support clinical data review and process efficiency.
The Clinical Programmer will lead clinical programming activities across one or more studies.
This role reports to Senior Director, Data Management, Oncology.
Key ResponsibilitiesCreates standard and/or custom programs/reports using data analytics tools such as SAS, Tableau, or other data visualization tools to support data oversight and review by data managers or other data reviewers.
Collaborates with Data Management, Clinical Development, Clinical Operations, Drug Safety, Statistical Programming, and Biostatistics to develop standard and custom data reports for quality data oversight / clinical data review.
Generates safety surveillance and/or safety quality data review outputs and patient profiles for Drug Safety and Clinical Development clinical data review.
Provides leadership, training, guidance, and support to other department members on data review tools such as SAS.
Collaborates with clients, peers, programmers, project teams, and/or requestors to clarify and finalize data specifications; uses expanded technical skills to meet evolving project needs.
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 and Clinical Programming for clinical data review bridging activities, meetings, discussions.
Possesses and maintains a broad overall knowledge in the field of clinical programming and clinical data management by reading related literature, self-training, attending training classes, attending professional meetings, etc.
RequirementsBachelor s degree (or equivalent) in Science and/or Computer Systems/IT backgroundMinimum 4 years experience in a pharmaceutical/biotech settingAdvanced programming and analytical skills using BASE/SAS, SAS/STAT, SAS MACROSStrong knowledge of Oncology clinical trialsData Visualization tools (like Tableau, Spotfire) and Python programming language experience a plusAbility to work independently to create standard datasets, program edit checks and produce quality data review outputsGeneral knowledge of industry standards and best practices such as CDISC/CDASH, SDTM, data standardization.
(FHIR and OMOP a plus)Windows applications:
Word, Excel, PowerPoint, etc.
Excellent analytical, problem-solving, organizational, time-management, interpersonal and communication skills Comfortable developing and debugging programs independently and without supervisionGood written and oral presentation skills and ability to communicate effectively to other programmers and non-technical colleaguesAbility to think creatively and independently, and to form sound opinions and make sensible decisions in a dynamic environmentThis position may be considered for remote only workThis is a contract position, estimated length of assignment - 6 monthsSalary range:
$60-$75/hr DOEA note to recruiters:
We do not allow external search party solicitation.
Presentation of candidates without written permission from the Ascendis Pharma Inc Human Resources team (specifically from:
Talent Acquisition Partner or Human Resources Director) is not allowed.
If this occurs your ownership of these candidates will not be acknowledged.
Job SummaryID:
8E52BE91EEDepartment:
Oncology, Clinical Operations, Oncology.
Estimated Salary: $20 to $28 per hour based on qualifications.
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