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Job title: Clinical Data Manager
Location: King of Prussia, PA
RATE OF PAY: Up to $(phone number removed) per year
Mode: All On-site
Type: Full Time
JOB DUTIES:
Duties:

• Develop, configure, and verify clinical databases and electronic data capture (EDC) systems, including case report forms (CRFs).
• Design and Implement detailed data management plans covering coding, data transfer, discrepancy management, workflow, reporting, and data validation.
• Generate and review Data cleaning listings such as offline listings, medical coding listings and missing pages reports.
• Conduct data entry, cleaning, validation checks, and resolve discrepancies to uphold data accuracy, completeness, and compliance with quality standards.
• Collaborate with cross-functional study teams to resolve data-related issues, integrate feedback, and align data management practices with study protocols.
• Adhere to Good Clinical Practice (GCP) and CDISC standards.

REQUIREMENTS:

• Bachelor's degree in health administration, Public Health or Life Sciences or Computer Science, or related discipline.
• 60 months of experience as Clinical Data Manager, Clinical Data Specialist, Program/Clinical manager or similar role.

Email resume to: (url removed)
Posted on: 9/4/2026

Job title: SR. Clinical Data Manager
Location: King of Prussia, PA
RATE OF PAY: Up to $96,013.00 per year
Mode: All On-site
Type: Full Time

Duties:

• Serve as the subject matter expert for the planning, set-up, and acquisition of external clinical data at the study level and manage study start up, conduct and close out activities.

• Create external data transfer agreements, ensuring external clinical trial data are aligned with company Standards and specifications to support data integration, analysis, and reporting.

• Help and advice in setting up infrastructure for external data, to flow into company Clinical data pipelines.

• Responsible for validation of all 3rd Party Data generated in clinical trial into company Clinical Data pipelines.

• Develop strong and productive working relationships with key stakeholders like Clinical Data Management, Clinical Data Engineering, Standards and other Study Execution Team members.

• Participate in preparing function for submission readiness and may represent Clinical Trial Tools & Technologies (CT3) group in a formal inspection or audit.

• Representing company in interactions with key external partners as part of company CT3 3rd Party Data Acquisition team.

• Responsible for timely submission and on-going maintenance of study related 3rd Party Data Acquisition documentation in TMF.

• Follow procedural documents and participating in reviewing and updating documents to make sure they are reflective of industry standards and regulatory requirements and include optimal processes.

• Follow procedural documents and participating in reviewing and updating documents to make sure they are reflective of industry standards and regulatory requirements and include optimal processes.

• Escalate issues to CT3 leadership appropriately.

 

REQUIREMENTS:

• Master's degree in public administration in Epidemiology and Biostatistics or related discipline.
• 24 months experience as Clinical Data Manager, Statistician, Biostatistician or related occupation.
• Must also have experience with at least one of the following areas/technologies also required: Clinical Data Capture: Medidata Rave, Sitero, Medrio, Phase Forward InForm
• Data Analysis: SAS or similar technologies.

Email resume to: (url removed)

Posted on: 9/4/2026