Jobs at ICON plc

Designs and supports clinical data management activities including eCRF maintenance, data reconciliation, validation specification upkeep, metrics tracking, issue resolution, and stakeholder communication to ensure high-quality trial data.

The Proposals Development Associate will lead client proposal preparation, collaborate with teams, conduct research, manage proposal workflows, and maintain proposal resources.

The Talent Acquisition Business Partner is responsible for executing recruitment strategies, managing the hiring process, and ensuring a positive candidate experience while collaborating with hiring managers and utilizing data insights.

As a Senior Investigator Pricing Analyst, you will analyze and develop pricing strategies for clinical trial investigators, ensuring accuracy and compliance with regulations.

The Principal Biostatistician will lead statistical strategy for oncology trials, mentor junior statisticians, and ensure regulatory compliance in analyses.

Manage day-to-day operations of clinical trials, ensuring adherence to quality and timelines, collaborating with teams, and maintaining compliance with regulations.

Oversee cardiovascular clinical trials, ensuring compliance with regulations while managing site relationships and communication. Requires 3 years of monitoring experience and strong problem-solving skills.

As a Clinical Research Associate II/Senior CRA, you will monitor clinical trials, ensure compliance, handle data reviews, and collaborate with site staff.

Lead preparation and submission of regulatory documents for study initiation, coordinate with stakeholders to obtain approvals, maintain regulatory records, advise study teams on compliance (ICH-GCP/local regulations), and participate in process improvement to streamline study start-up activities.

As a Clinical Research Associate II, you will manage clinical trials ensuring compliance, data integrity, and patient safety while collaborating with site staff.

The Clinical Trial Manager oversees the planning, execution, and completion of clinical trials. This involves managing timelines, budgets, regulatory compliance, and site relationships, while leading cross-functional teams to ensure successful trial outcomes.

As a Project Manager at ICON, you will lead project activities, ensuring timely delivery within budget and quality standards while coordinating teams and managing stakeholder communications.

As a Clinical Research Associate II, you will oversee clinical trials, ensuring compliance, data integrity, and patient safety through site visits, collaboration, and documentation preparation.

Lead monitoring and management of clinical trial sites to ensure protocol compliance, GCP adherence, data integrity, and participant safety. Conduct site visits, resolve issues, train site staff, collaborate with cross-functional teams, and maintain stakeholder relationships to support successful trial execution.

As a Clinical Research Associate, you will liaise with investigational sites, ensuring compliance, monitoring studies, maintaining documentation, and supporting recruitment efforts in oncology trials.

Lead monitoring and oversight of clinical trial sites to ensure GCP, protocol and regulatory compliance. Conduct site visits, manage multiple sites, support data integrity and participant safety, provide training and guidance to site staff, collaborate with cross-functional teams, and build strong site relationships to facilitate successful oncology trial execution.

Oversee and manage clinical trial activities, ensuring compliance with protocols and regulations. Collaborate with teams, conduct site visits, and support data integrity and participant safety.

Oversee and monitor clinical trial sites to ensure protocol, regulatory and GCP compliance; conduct site visits; manage multiple sites; ensure data integrity and participant safety; train and support site staff; collaborate with cross-functional teams and maintain stakeholder relationships.

Monitor clinical trial sites for adherence to protocols, conduct site visits, provide training, and manage relationships with stakeholders.

The Senior Clinical Research Associate oversees clinical trials, ensuring adherence to protocols and regulatory standards, conducting site visits, and managing relationships with stakeholders.