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Clinical Data Management Trainee Jobs (NOW HIRING)

Clinical Data Management (CDM) supports drug discovery, development and marketed products across Gilead by ensuring the accurate and timely acquisition, analysis and reporting of diverse clinical ...

Develop and implement data management plans. * Create and maintain validation plans for clinical databases. * Develop and implement data surveillance plans for clinical trials. * Identify and ...

Provide direction of activities of Clinical Data Management (CDM) team members regarding completion of project deliverables to ensure they are on schedule according to quality standards, requirements ...

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Clinical Data Management Trainee information

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How much do clinical data management trainee jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for clinical data management trainee in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.

What are the most commonly searched types of Clinical Data Management jobs?

The most popular types of Clinical Data Management jobs are:

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Infographic showing various Clinical Data Management Trainee job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $118,909 per year, or $57.2 per hour.

Specialists, Clinical Data Management

Rahway, NJ โ€ข On-site

Scorpion Therapeutics
51 - 200 employees

Other

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago


Job description

Primary Responsibilities:
  • Design, build, maintain, test, and document data review based on written specifications.
  • Review technical feasibility of study-team proposed programming/reporting and technically implement; collaborate across teams and communicate issues/ideas while understanding protocol.
  • Support development and reporting for data cleaning, medical review, clinical monitoring, and safety reports for quality and timely availability.
  • Provide ongoing support for In-Life Reports.
  • Ensure Change Requests and Incident Reports are documented, signed off, tracked, and reported to upper management.
  • Participate in study improvement initiatives (e.g., automation), testing of new systems, and ongoing training/mentoring.
Education:
  • Associate degree + 3+ years in clinical data programming/data engineering or related functions, OR
  • Bachelorโ€™s degree + 2+ years in related clinical data programming/data engineering/clinical operations functions, OR
  • Advanced degree preferred (masterโ€™s/doctorate) with experience in clinical development and/or related activities.
Required Knowledge & Skills:
  • Proficiency in clinical data/reporting systems (e.g., Databricks, Python, SAS, SQL/PL/SQL, Power BI) and AI tools.
  • MS Windows/Office knowledge; exposure to web-based applications.
  • System Development Lifecycle Management/system validation knowledge.
  • Strong relationships, urgency/customer focus, communication with study teams, organization/problem-solving, ability to learn, multitask and work independently.
  • Understanding of drug discovery process, FDA regulations, GxP, and ICH.
Required Skills (examples):
  • Clinical Data Management, Communication, Programming, Data Analysis/Quality Assurance, EDC, PL/SQL, SQL databases, team communication.
Benefits:
  • comprehensive benefits including medical/dental/vision, retirement (401(k)), paid holidays, vacation, and compassionate/sick days.
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