FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
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, project planning, and execution within the clinical research domain, ensuring high-quality deliverables and compliance with timelines. Proficient in leading teams, managing stakeholder communications, and implementing process innovations.
Highest-signal resume keywords
Data Management ExpertiseProject Planning and ExecutionClinical Research Process KnowledgeTeam LeadershipAdvanced Computer Applications
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 CleaningProject ManagementValidation of Device IntegrationsFinancial ManagementCore Operating Procedures Development
Soft Skills
Collaborative CommunicationStakeholder EngagementTraining and Mentoring
Tools & Technologies
Microsoft ExcelMicrosoft WordDatabase Management Systems
Industry Keywords
Drug Development LifecycleClinical Data ManagementStudy Setup RequirementsSponsor AuditsScope of Work (SOW)
About the role
Key responsibilities & impact- Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction.
- Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs.
- Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables.
- Gather Study Set up requirements through discussion and communication with relevant stakeholders.
- With Minimal guidance - support, overview of validation of new Device integrations.
- Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.
- Ensure that all the deliverables are of expected quality standards and meet customer expectations.
- With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW).
- Support Training of New joiners.
- Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.
- Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended as required.
- With Guidance manage & oversight the implementation of new technology / database revisions.
- Work closely with the programming team for process innovation and automation.
- Be compliant to trainings and eSOP reading.
- Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
- Communication with Line Manager, and other team members across functions should be collaborative.
Requirements
What you’ll need- Bachelor's Degree In health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management
- 3 -4 years direct Data Management experience, including a minimum of 1 year as a CDM project lead.
- English Fluency Spoken and English Advanced
- Advanced computer applications like Microsoft excel, word, Inbox etc
- Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process
Benefits
Comp & perks- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
