Lead Clinical Data Manager

ICON plc

Lead Data Manager at ICON responsible for overseeing clinical data management and ensuring adherence to regulations. Collaborate with teams to contribute to innovative treatments and therapies.

Posted 7/29/2026full-timeRemote • Pennsylvania • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical data management, including proficiency in CDISC standards and regulatory compliance, while providing leadership to cross-functional teams and optimizing data management processes.

Highest-signal resume keywords

Clinical Data ManagementCDISC StandardsEDC SystemsLeadershipRegulatory Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data ManagementData ReviewData ReconciliationData Management ProcessesRegulatory Requirements

Soft Skills

CommunicationLeadershipProblem-SolvingTeam CollaborationTime Management

Tools & Technologies

RaveInformMedidata

Industry Keywords

PharmaceuticalBiotechnologyCROFDA RegulationsEMA RegulationsICH-GCP Guidelines

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead and oversee the planning, execution, and delivery of clinical data management activities for assigned projects
Collaborate with cross-functional teams to develop data management plans and ensure adherence to regulatory requirements and industry standards
Provide leadership and guidance to data management team members throughout the lifecycle of clinical trials
Perform data review and reconciliation activities to ensure accuracy, completeness, and consistency of clinical data
Contribute to the development and implementation of data management processes and best practices to optimize efficiency and quality

Requirements

What you’ll need

Bachelor's degree or higher in a relevant scientific discipline
Minimum of 4-5 years of experience in clinical data management within the pharmaceutical, biotechnology, or CRO industry
Proficiency in CDISC standards, FDA/EMA regulations, and ICH-GCP guidelines
Strong technical skills with experience in EDC systems and data management tools (e.g., Rave, Inform, Medidata)
Excellent communication, leadership, and problem-solving skills with the ability to work effectively in a team environment and manage multiple priorities simultaneously
Willingness to travel as required (approximately 10%)

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