Clinical Study Operations Specialist

ICON Strategic Solutions

Wilmington (DE)

Hybrid

USD 65,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Health and wellbeing programs

Retirement plan

Life insurance

Employee assistance program

Learning and development opportunities

Hybrid work model

Job summary

ICON is a global healthcare intelligence and clinical research organization dedicated to bringing new medicines to patients faster. The role works in a hybrid Wilmington, DE setting to coordinate translational medicine activities and support protocol development, biospecimen logistics, and data management across study teams.

The ideal candidate has a scientific background with 2+ years in clinical drug development, familiarity with ICH/GCP, and strong communication skills to collaborate across

Qualifications

Scientific background with 2+ years’ experience in clinical drug development or clinical trial execution.
Experience with biospecimen collection procedures and logistics.

Responsibilities

Coordinate translational medicine objectives with study teams during protocol development and execution.
Support biospecimen collection and analysis during protocol development, study start-up and amendments.
Assist Data Management with eCRF setup and sample tracking/reconciliation.

Skills

Translational Medicine

Clinical study coordination

Biospecimen handling

Data management

GCP/ICH knowledge

Microsoft Office

Communication skills

Education

Biological sciences degree or nursing or Med Tech

Tools

eCRF / EDC systems

Sample management systems

Job description

The ideal candidate has a scientific background with 2+ years in clinical drug development, familiarity with ICH/GCP, and strong communication skills to collaborate across

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