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Tier-1 employer and mid-level generalist CDM role, increasing applicant competition.
Clinical data management and drug development expertise limits transferability across industries.
Explicit 3–4 years experience plus mandatory CDM lead and clinical trial knowledge narrows candidate pool.
Manage end-to-end delivery of data management services for single or multi-service clinical research projects ensuring quality, timeliness, budget compliance, and customer satisfaction.
Provide leadership and expertise to the Data Management team, overseeing project planning, execution, financial management, risk handling, and communication with stakeholders.
Lead data validation, cleaning activities, and ensure compliance with quality standards; support training of new team members and participate in sponsor meetings and audits.
Bachelor's degree in health, clinical, biological, mathematical sciences, or related field.
3-4 years of direct Data Management experience, including at least 1 year as a Clinical Data Management project lead.
Advanced proficiency in English (spoken and written) and advanced computer skills including Microsoft Excel, Word, and email.
Advanced understanding of drug development lifecycle and overall clinical research process.
Experienced in clinical or drug development data management with leadership in managing project delivery and team guidance.
Capable of independently managing project risks, timelines, and stakeholder communications in a regulated environment.
Familiar with clinical study data validation, cleaning processes, and implementation of new technologies or database revisions.