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 data management, clinical trial processes, and quality management, with a strong ability to lead project teams and implement effective solutions. Proficient in EDC systems, particularly RAVE, and skilled in developing data management plans and metrics to enhance project performance.
Highest-signal resume keywords
Data Management LeadershipEDC ExperienceClinical Trial Process KnowledgeQuality Management ExpertiseCommunication and Presentation Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Data Management PlansClinical Data Model DevelopmentData Validation ChecksMetrics and ForecastingCRF/eCRF AnnotationRisk ManagementResource ManagementProcess ImprovementProject-Specific Data ManagementPerformance Review Assessments
Soft Skills
Team LeadershipProblem SolvingCollaborationEncouraging Team SolutionsClient Liaison
Tools & Technologies
RAVEEDC SystemsData Management SystemsClinical Data Review ToolsDiagnostic Specifications
Certifications & Qualifications
University/College Degree in Life ScienceNursing CertificationMedical Technology CertificationLaboratory Technology Certification
Industry Keywords
Clinical OperationsBiometricsCRO IndustryPharmaceutical CompaniesBiotechnological Companies
About the role
Key responsibilities & impact- Serve as the technical leader on all data management aspects for projects, including start-up, maintenance, and completion activities
- Develop global Data Management Plans and Quality Management Plans
- Identify and implement solutions to project data management issues and concerns, including proactive prevention strategies based on metrics and forecasts
- Serve as project and client liaison, managing and providing project-specific data management status, cycle time, and productivity metrics
- Coordinate and participate in development of the clinical data model and/or database design and annotate CRFs/eCRFs
- Review data acquisition conventions, data review guidelines, and diagnostic specifications
- Coordinate development and testing of data management system edit/data validation checks, diagnostics, and special listings/procedures
- Collaborate with clinical, programming, statistics, CDM technical support, drug safety, and other project and specialty teams
- Lead advanced planning and risk management, including issue escalation and resource management
- Oversee technical performance of data review project staff and delivery of quality data on time and on budget
- Assist with goal creation and performance review assessments for data review project staff
- Maintain technical data management competencies through internal and external training seminars
- Ensure project staff are trained and adhere to project-specific and global standardized data management processes
- Identify process and efficiency improvements and implement solutions
- Support achievement of project revenue and operating margin targets for data management activities
- Support business development through data management time and cost estimates and presentations to potential clients
Requirements
What you’ll need- University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
- Additional relevant work experience will be considered in lieu of formal qualifications
- Lead experience across a mix of therapeutic areas especially across Late Phase (IIb-III) trials
- EDC experience; ideally RAVE experience, with experience across other EDCs advantageous
- Excellent oral and written communication and presentation skills
- In-depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations
- Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical/biotechnological companies
- Ability to lead project teams on project strategies and achievement of department goals, objectives, and initiatives
- Willingness to encourage team members to seek solutions
Benefits
Comp & perks- Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
- A genuine work life balance
- Flexibility in working hours
- A thorough onboarding with support from your personal mentor
- A permanent employment contract with Fortrea