Instagram
youtube
Facebook

Senior Clinical Data Science Lead

6+ years
Not Disclosed
10 April 18, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:

Senior Clinical Data Science Lead


Location:

United States (Remote)


Job ID:

2025-118366


Department:

Clinical Data Management (ICON Strategic Solutions)


Job Type:

Full-Time, Remote


Application Contact:

Name: Brendan Hoey
Message Option: Send a message via job platform
Other Roles: View other roles by Brendan


Job Description:

About ICON:
ICON plc is the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence, offering leading-edge solutions across clinical trials.


Key Responsibilities:

  • Coordinate Clinical Data Management (CDM) process initiatives, including project management, process definition, implementation, change management, and training plans.

  • Provide regular updates to CDM staff on CDM operational activities, including process alerts and training updates.

  • Support the development and revision of CDM processes for both outsourced and in-house studies.

  • Act as a point of contact for CDM staff on key process topics related to data management activities.

  • Collaborate with key stakeholders to manage EDC local lab activities.

  • Maintain the CDM Subject Matter Expert (SME) network and facilitate updates and discussions.

  • Support the Learning Management System (LMS) and role assignments for CDM staff.

  • Assist with quality assurance activities related to inspections and audits, in collaboration with the CDM Operations Compliance & Quality team.


Qualifications & Experience:

  • 6+ years of experience in data management and/or drug development, with expertise in cross-functional interfaces with data management.

  • Solid understanding of clinical trial documents and processes (protocols, CRFs, study reports, etc.).

  • Proven project management skills, with experience managing large drug development programs.

  • Knowledge of GCP, ICH, and regulatory guidelines as they relate to clinical data management.

  • Experience in therapeutic areas such as oncology, cell therapy, neuroscience, vaccines, etc., is preferred.

  • Experience with regulatory inspections (FDA, EMA, etc.) is a plus.

  • Strong knowledge of data management best practices and technologies.

  • Expertise in drug development processes and cross-functional collaboration.


ICON Employee Benefits Include:

  • Generous annual leave

  • Multiple health insurance plan options

  • Competitive retirement savings plans

  • Global Employee Assistance Programme (TELUS Health)

  • Life assurance

  • Country-specific optional benefits, such as:

    • Childcare vouchers

    • Bike-to-work schemes

    • Discounted gym memberships

    • Subsidized travel passes

    • Health assessments

More information: ICON Benefits Overview


Diversity & Inclusion Commitment:

ICON fosters a diverse and inclusive workplace, where all qualified applicants are encouraged to apply regardless of their background.