Clinical Data Coordinator — Data Validation & Analysis

Medpace, Inc.; Stirling; On-site; GBP 26,000 - 38,000; Full time

Benefits offered by this job

Office based culture

Mentorship on-site

Defined career paths

Onboarding & training programs

Continuous learning opportunities

Company-sponsored social events

Job summary

Medpace, Inc. is seeking a full-time, office-based Data Coordinator in Stirling to join the Data Management team. You will analyse clinical data to ensure accuracy and support project efforts, with extensive onboarding to become a data expert.

This role offers training and the opportunity to grow within a leading CRO. As part of a collaborative team, you will work on diverse projects, validate database designs, report trends, resolve data conflicts, and maintain study documentation in a

Qualifications

• Bachelor's degree in Life Sciences or Mathematics.
• Strong attention to detail.
• Excellent working knowledge of Microsoft Excel and Word.
• Solid oral and written English language communication skills.

Responsibilities

• Participate as part of a team on various project(s)
• Validate an entry database design
• Report metrics and data trends on projects
• Identify data conflicts and issues on projects
• Collaborate with research sites globally to resolve data conflicts
• Reconcile data from multiple sources
• Create and update study documentation on projects

Skills

Attention to detail

English communication

Education

Bachelor's degree in Life Sciences or Mathematics

Tools

Microsoft Excel

Microsoft Word

Job description

Medpace, Inc. is seeking a full-time, office-based Data Coordinator in Stirling to join the Data Management team. You will analyse clinical data to ensure accuracy and support project efforts, with extensive onboarding to become a data expert.

This role offers training and the opportunity to grow within a leading CRO. As part of a collaborative team, you will work on diverse projects, validate database designs, report trends, resolve data conflicts, and maintain study documentation in a