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# Salesforce Developer

- **Company:** CareerCircle
- **Location:** Rahway, NJ, United States (Remote available)
- **Experience:** Expert
- **Salary:** $140,400.0
- **Contract:** Permanent contract
- **Skills:** Artificial Intelligence, Data Analysis, Clinical Data Management, Clinical Data Repository, Clinical Trial Management Systems, Software Documentation, Computer Programming, Data Architecture, Data Validation, Data Cleansing, Information Engineering, Data Governance, Data Integration, Data Integrity, Data Structures, Data Visualization, Relational Databases, Decision Support Systems, Programming Tools, Electronic Data Interchange (EDI), Electronic Data Capture, File Transfer, Metadata, Operational Databases, Scrum Methodology, DataOps, SAS (Software), Semantic Web, Software Engineering, Tableau (Software), Clinical Data Management System, Enterprise Software Applications, Generative AI, Information Technology, Collibra, Data Programming, Data Analytics, Data Management, Spotfire, Veeva, VeevaVault
- **Published:** September 26, 2026
- **Apply:** https://www.careercircle.com/jobs/all/all/usa/nj/basking-ridge/90723903-e7f6-4bea-84b6-3043f5c3d3dc

## About the Role

Bachelor' s Degree Required. Master's Degree preferred.

Minimum of 5 years of Global Clinical Trial Experience in the device/pharmaceutical/CRO industry; expertise in Clinical Programming, methods, and techniques; expertise in the use of standard reporting and data visualization tools including Spotfire, Tableau, JReview and SAS tools; knowledge of CDISC and CDASH standards; knowledge and understanding of industry standard clinical technologies including EDC, CTMS, and IRT. Required

Additional Skill:

 * Expertise in Clinical Programming, methods, and techniques
 * Work collaboratively with people at different levels of experience, different disciplines, and cultures
 * Self-directed; able to work independently
 * Critical thinking and complex problem-solving skills
 * Ability to manage multiple priorities
 * Strong background in programming development, project management, validation, execution, maintenance, documentation, and archival of clinical data
 * Knowledge:
 * Expertise in supporting and handling external data; viewing and integrating data in multiple formats including SAS
 * Proficient in industry standards, medical terminology, and clinical trial methodologies
 * Experience with industry standard reporting and data visualization tools
 * Experience with one or more industry standard clinical technologies such as CTMS, EDC (RAVE, InForm), Veeva Vault, IRT, and Clinical Portals
 * Knowledge and understanding of data standards - CDASH, SDTM/ADaM, CDISC
 * Knowledge and understanding of relational databases, Leadership
Automation
Governance
Innovation
Creativity
Statistics
Compassion
Scalability
Informatics
Data Quality
Data Science
Data Analysis
Presentations
Data Integrity
Regulatory CMC
Bioconjugation
Business Acumen
Problem Solving
Data Management
Computer Science
Telephone Skills
Change Leadership
Organic Synthesis
Biopharmaceuticals
Influencing Skills
Advanced Analytics
Business Valuation
Strategic Thinking
Leadership Studies, Regulatory Compliance
Scientific Literature
Stakeholder Management
Stakeholder Engagement
Digital Transformation
Mathematical Chemistry
Professional Networking
Computational Chemistry
Pharmaceutical Sciences
Self Service Technologies
Data-Driven Decision Making
Product Lifecycle Management
Scrum (Software Development)
Continuous Improvement Process
Enterprise Application Software
Generative Artificial Intelligence
Biologics License Applications (BLA), Leadership
Management
Innovation
Biomarkers
Immunology
Collections
Peer Review
Data Quality
Self-Starter
Life Sciences
Data Exchange
File Transfer
Data Cleansing
Data Reporting
Pharmaceuticals
Clinical Trials
Data Structures
Decision Making
Immune Disorder
Data Management
Medical Devices
Data Collection
Drug Development
Data Integration
Data Acquisition
Vendor Management
Trial Master File
Solution-Oriented
Industry Standards
Data Documentation
Emerging Technologies
Operational Databases
Cardiovascular Disease
Sustainable Development
Pre-Clinical Development
Clinical Data Management
Interpersonal Communications
Electronic Data Capture (EDC)
Good Clinical Practices (GCP)
Continuous Improvement Process

## Description

Oncology
Auditing
Timelines
Leadership
Management
Governance
Innovation
Data Quality
Data Analysis
Biostatistics
Collaboration
Accountability
SAS (Software)
Data Integrity
Data Reporting
Pharmaceuticals
Clinical Trials
Immune Disorder
Data Management
Data Validation
Critical Thinking
Programming Tools
Impact Assessment
Project Management
Influencing Skills
Data Visualization
Industry Standards
Medical Terminology
Relational Databases
Cardiovascular Disease
Regulatory Requirements
Complex Problem Solving
Sustainable Development
Data Visualization Software
Standard Operating Procedure
Electronic Data Capture (EDC)
Milestones (Project Management)
Clinical Trial Management Systems
Spotfire (Data Analytics Software)
Tableau (Business Intelligence Software), The Manager, Data Programming, Analytics, and Reporting is a member of the Biostatistics and Data Management team and serves as a subject matter expert for Clinical Data Programming, Reporting, Data Visualizations, and supporting programming tools. This position will manage the accountability for the quality and delivery of Programming deliverables consistent with business needs of each study team conforming to programming standards and specifications across clinical studies.

The scope of work includes oversight and expertise in the design, development, and validation of programs, standard and adhoc reports, standard and exception data listings, and visualizations using SAS or visualization software such as Spotfire or JReview to support ongoing data review activities, achieve critical study milestones, and gain data insights into our clinical studies. The position requires good understanding of programming methods and techniques, critical thinking, and complex problem-solving skills. This position will require strong collaboration in working with other members of the Biostatistics and Data Management, external CRO partners, service providers, and other stakeholders.

Responsibilities

Leadership, Direction and Strategy:

 * Manages accountability for the quality and timely delivery of the Data Management Programming, Reporting, visualizations, and data listings across clinical studies.
 * Mentors and trains Data Validation and Reporting Specialists as needed.
 * Contributes to the development of Standard Operating Procedures (SOPs), policies, and guidelines.
 * Provides insights and/or recommendations to streamline data management information flow, enhance business efficiencies, and improve quality.
 * Provides training on the data visualization software as required.
 * Is accountable for Clinical study data programming deliverables meeting quality and time expectations for assigned studies.
 * Proactively identifies and manages risks to data quality, data integrity, and timelines with respect to regulatory submissions.
 * Builds business relationships with other line functions; is an ambassador and Programming SME.
 * Provides information pertaining to programming for audits and regulatory inspections.
 * Promotes Daiichi Sankyo values and quality workplace culture, collaboration in cross-functional and multicultural settings, and builds and maintains positive relationships with internal/external stakeholders/vendors/partners.

Project Management:

 * Manages the quality and delivery of the Clinical study data programming deliverables for assigned studies including edit checks programming, complex reports, and listings; patient profiles, subject narratives, exception listings, dose modification reports, and other adhoc reports as part of standard data validation and reporting package for clinical studies.
 * Provides oversight on the programming specifications for the data validation and reporting deliverables; code, test, and document deliverables conforming to programming standards, data quality and governance, and validation policies.
 * Partners with the study data managers to develop and confirm programming specifications, support adhoc external data reporting and listings needs, and manage quality expectations in collaboration with internal and external stakeholders.
 * Proactively identifies and resolves issues that may influence and/or impact study quality and other deliverables.
 * Manages and mitigates quality and delivery risks to ensure adherence to timelines, and quality thresholds.
 * Is accountable for inspection readiness of Programming documentation filed/archived according to applicable Daiichi Sankyo and regulatory requirements., Veeva
DataOps
Coaching
Metadata
Leadership
Management
Governance
Innovation
Semantic Web
Communication
Advertisement
Data Modeling
Pharmaceuticals
Data Governance
Data Management
Team Leadership
Data Engineering
Data Architecture
Influencing Skills
Collibra (Software)
Delivery Performance
Alation Data Catalog
Operational Excellence
Software Documentation
Artificial Intelligence
Product Lifecycle Management
Continuous Improvement Process


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