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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical data management systems and data analysis, with a strong ability to design and implement clinical systems. Proficient in CRF design and technical specification development, ensuring adherence to study protocols and effective communication.
Highest-signal resume keywords
Clinical Data ManagementMedidata RaveVeeva EDCData AnalysisCRF Design
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Database DevelopmentTechnical Specification CreationData Validation OutputsData Analytics OutputsCustom Output ProgramsQuality Control Peer ReviewsPrototyping MethodologiesEDC IntegrationIssue TrackingStudy Protocol Adherence
Soft Skills
Excellent Written CommunicationExcellent Verbal Communication
Certifications & Qualifications
Bachelor’s Degree
Industry Keywords
Clinical ResearchCRF Design ToolsClinical Trial ProtocolsStudy Set-UpProject Management
About the role
Key responsibilities & impact- Assist with development of Custom CRF screens, Edit Check, and Dynamic Check specification documents, using prototyping methodologies as needed
- Assist with creation of technical specifications for output programming, including Data Validation Outputs, Data Analytics outputs, and custom output programs
- Copy and modify CRFs from standard libraries and other studies under specific instruction
- Read, understand, and adhere to study protocols, contracts, and scopes of work during study set-up, maintenance, and close-out
- Track issues that may affect project target dates, scope, or budget and escalate potential problems effectively and timely
- Consolidate and complete high-level system requirements documents and facilitate their review with support
- Perform quality control peer reviews of database-related specifications and record comments appropriately with support
- Support senior project leads in eCRF and other specification review meetings
- Support simple to medium migration/post-production change activities
- Assist with EDC integration-related activities
Requirements
What you’ll need- 6+ months of experience in the design and implementation of clinical systems within the clinical research industry
- Expertise in data analysis and interpretation or Database Development, with proficiency in clinical data management systems and software
- Experience with Medidata Rave and/or Veeva EDC
- Functional knowledge of CRF design tools and ability to plan and design CDMS components directly from interpretation of medium complexity clinical trial protocols
- Excellent written and verbal communication skills
- Bachelor’s Degree in a relevant field
- Applications must be submitted in English
- Legal right to work in the country where the role is based
Benefits
Comp & perks- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways