clinical trial associate

ICON plc is a world-leading healthcare intelligence and clinical research organization. We are seeking a Clinical Trial Associate to assist with the design and analysis of clinical trials, interpreting complex medical data, and advancing innovative treatments.Based remotely in Mexico, you will support regulatory readiness, monitor trial activities, manage...

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within the timelines agreed with project management and Site...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Clinical Trial Manager - HomebasedICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and...

Clinical Trials BookkeeperJob DescriptionKey Responsibilities:Track all outstanding receivables related to clinical trials, including sponsor payments, and reimbursements.QC patients visits; prepare and issue invoices in accordance with contract milestones and payment schedules.Follow up regularly with sponsors, CROs, to ensure timely payment.Maintain...

Job OverviewPrimary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within the timelines agreed with project management and Site...

About the role The Clinical Trial Manager (CTM) will work collaboratively across cross-functional teams with Project Management, Clinical Operations, Data Management, Medical Monitoring, Pharmacovigilance, and Regulatory Affairs while understanding and managing client expectations. The Clinical Trial Manager is responsible for the day-to-day management of...

About the roleThe Clinical Trial Manager (CTM) will work collaboratively across cross-functional teams with Project Management, Clinical Operations, Data Management, Medical Monitoring, Pharmacovigilance, and Regulatory Affairs while understanding and managing client expectations. The Clinical Trial Manager is responsible for the day-to-day management of...

About the role The Clinical Trial Manager (CTM) will work collaboratively across cross-functional teams with Project Management, Clinical Operations, Data Management, Medical Monitoring, Pharmacovigilance, and Regulatory Affairs while understanding and managing client expectations. The Clinical Trial Manager is responsible for the day-to-day management of...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Project Manager at ICON, you will be responsible for leading and coordinate project...

Job Description: We are looking for a Part-Time Virtual Clinical Trial Navigator (Registered Nurse) based in the Philippines to provide one-on-one support to patients and families navigating the clinical trial process. This role requires strong communication, patient advocacy, and coordination skills, as well as experience in clinical research, patient...

Job Description: We are looking for a Part-Time Virtual Clinical Trial Navigator (Registered Nurse) based in the Philippines to provide one-on-one support to patients and families navigating the clinical trial process. This role requires strong communication, patient advocacy, and coordination skills, as well as experience in clinical research, patient...

Fortrea Philippines Inc. seeks a Regulatory Submissions Coordinator to act as primary contact with investigative sites during study maintenance and site startup activities, ensuring timely collection and quality review of essential documents for RA/IRB/IEC submissions.You will work under supervision to ensure compliance with ICH/GCP, SOPs, and local...

Signant Health is seeking a Solution Engineer to collaborate across Sponsors, Clinical and GPM teams to design trial solutions using Signant’s product portfolio. You will translate study protocols into system requirements, considering eCOA best practices and project constraints.You will gather information from multiple sources, draft validation and process...

IQVIA is seeking a Records Management professional to act as liaison between Records Management and user departments for Trial Master files. You will apply regulatory and SOP-based expertise across multiple projects, sites, and teams. Responsibilities include imaging, transfer, retention, and disposition of records, ensuring quality, timelines, and security....

Signant Health is seeking a Solution Engineer to design and deliver clinical trial solutions. You will analyze study protocols, translate requirements into system specs, and work across Sponsors, Clinical and GTD teams to ensure feasible, on-time delivery.You will develop functional requirements, maintain documentation, and support validation activities...

ICON is seeking a Clinical Trial Associate for an office-based hybrid role in Manila. You will support site monitoring, ensure protocol adherence, and help maintain efficient trial operations. The role requires a life sciences/clinical research background, strong organization, and excellent communication. Hybrid work with 2–3 days on-site at Makati ensures...

Angel City VA Recruitment is seeking a Business Development Associate to drive end-to-end pipeline development for clinical trials and identify opportunities through ClinicalTrials.gov, GlobalData, and sponsor/CRO sites.You will maintain an Excel/SharePoint tracker with real-time updates on study status, sponsor, therapeutic area, and timelines, and perform...

Genesis Clinic in the Chicago area is seeking a remote Patient Recruiter to support enrollment across multiple active clinical trials in endocrinology, metabolic health, and orthopedics. You will be the first point of contact for potential study participants and pre-screen patients from our database.This remote role requires excellent English, comfort making...

Thermo Fisher Scientific is seeking a Clinical Trial Manager to lead clinical operations across studies of varying complexity. The role focuses on delivering high-quality data within contract scope while maintaining profitability through efficient team management.You will work with cross-functional teams to develop Monitoring Plans, ensure trial master file...