FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Clinical Data Management, including data review, eCRF development, and third-party data reconciliation. Proficient in utilizing Clinical Data Management Systems and standard software applications to support clinical research protocols.
Highest-signal resume keywords
Clinical Data Management ExperienceKnowledge of Clinical Data Management SystemsData Review and Analytic SkillsExcellent Written and Oral Communication SkillsBasic Knowledge of Drug Development Process
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Data ManagementData ReviewECRF DevelopmentData Validation SpecificationsData ReconciliationAnalytic Requirements ExecutionLocal Lab Data EntryLocal Lab Data ReviewClinical Research ProtocolsStudy Specific Procedures
Soft Skills
Excellent Communication Skills
Tools & Technologies
Medidata RAVEInFormVeevaWindowsMS Office
Industry Keywords
Clinical Research OrganizationPharmaceutical CompanyDrug Development Process
About the role
Key responsibilities & impact- Perform routine reviews of clinical and third-party data for subjects enrolled in clinical research protocols based on edit check/output specification documentation
- Maintain clinical data management-related study documentation as appropriate
- Perform local lab data entry and local lab data review activities as required
- Execute data review and analytic requirements on low- to medium-complexity work
- Manage the third-party data reconciliation process
- Assist the Clinical Data Science Lead in developing eCRFs, Data Validation Specifications, and Study Specific Procedures
Requirements
What you’ll need- 1-2 years of clinical data management experience in a clinical research organization or pharmaceutical company
- Basic knowledge of the drug development process
- Knowledge of at least 1 Clinical Data Management System (Medidata RAVE, InForm, Veeva, etc.)
- Strong knowledge of computerized information systems and standard application software (Windows, MS Office)
- Excellent written and oral communication skills
- Bachelor’s degree or local equivalent
- Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above
- Fluent English and host country language, in reading, writing, and speaking
- 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