Analyst, Global Data Manager

Job Overview

Analyst, Global Data Manager (GDM) – a hybrid, entry‑level, individual contributor role focused on data management and scientific data review across low to moderate complexity clinical trials. The position may be based in Spring House, PA;
Horsham, PA;
Raritan, NJ; or Titusville, NJ.

• Work with external suppliers, trial customers, and internal/external partners to establish, align, and confirm data management expectations for assigned trials.
• Gather and review content and integration requirements for Electronic Code of Federal Regulations (eCFR) and other data collection tools.
• Participate in establishing conventions, quality expectations, dataset content, and structure for clinical data.
• Set timelines, monitor delivery of data management milestones, and ensure deliverables are on time.
• Review clinical data management documents for quality, scientific content, organization, clarity, accuracy, format, and consistency.
• Facilitate compliance with regulatory guidelines and documentation matrix; support real‑time inspection readiness.
• Participate in regulatory agency inspections and internal audits as required.
• Support clinical working groups to meet data management and trial needs.
• Identify and communicate lessons learned and frequently asked questions at trial level.
• Contribute to functional plans such as the Integrated Review Plan.
• Participate in process, system, and tool improvement initiatives.
• Execute data management activities and perform oversight controls per procedures under DML direction.

• Bachelor’s degree in Clinical Data Management, Life Sciences, Computer Sciences, or related field.
• Clinical data management experience preferred.
• Knowledge of scientific concepts in clinical trial protocols preferred.
• Experience in clinical drug development within pharma, CRO, or related industry preferred.
• Understanding of international data management guidelines preferred.
• Familiarity with industry standards such as CDISC, SDTM, CDASH, etc. preferred.
• Knowledge of technology platforms for data exchange and project management preferred.
• Excellent verbal and written communication skills.
• Ability to adapt to a rapidly changing environment.
• Collaborative approach across all management levels preferred.
• Up to 10% travel required.

• Advanced Analytics
• Analytical Reasoning
• Biostatistics
• Business Behavior
• Clinical Data Management
• Clinical Operations
• Cross‑Functional Collaboration
• Database Applications
• Data Privacy Standards
• Data Savvy
• Execution Focus
• Good Clinical Practice (GCP)
• Process Oriented
• Project Support
• Report Writing
• Standard Operating Procedure (SOP)

The anticipated base pay range for this position is $76,000.00 – $.

• Pension and retirement plan (401(k)) participation
• Long‑term incentive program eligibility
• Vacation – 120 hours per calendar year
• Sick time – 40 hours per calendar year (48 hours in Colorado, 56 in Washington)
• Holiday pay and floating holidays – 13 days per calendar year
• Work/Personal/Family Time – up to 40 hours per calendar year
• Parental leave – 480 hours within one year of birth/adoption/foster care of a child
• Bereavement leave – 240 hours for immediate family (40 hours for extended family)
• Caregiver leave – 80 hours in a 52‑week rolling period (10 days)
• Volunteer leave – 32 hours per calendar year
• Military spouse time‑off – 80 hours per calendar year

Additional benefits information can be found at