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GE HealthCare is hiring a Biomedical Technician II to service customer biomedical equipment at customer sites. The role evaluates and repairs equipment, performs planned maintenance and inspections, supports customers and teammates, and helps ensure compliance with quality and safety requirements. Tags Health Care Life Science Pharmaceutical Artificial Intelligence (AI) Accounting Human Resources Healthcare Publishin

Fortrea is seeking a Clinical Research Associate II to support Phase I clinical trials. The role includes monitoring and managing study sites, protecting participant safety, ensuring data integrity, and coordinating clinical project activities. Tags Health Care Life Science Pharmaceutical Artificial Intelligence (AI) Accounting Human Resources Healthcare Publishing Biopharma Bookkeeping and Payroll Employment Freelan

Lifelancer lists this role on its talent-hiring platform; the hiring client is not identified. The Clinical Trial Coordinator II provides administrative and technical support to clinical trial project teams, including trial documentation, site activation, feasibility activities, and coordination with sites and internal teams. Responsibilities As part of our global team, you’ll have the opportunity to provide administ

Thermo Fisher Scientific is hiring an experienced Clinical Research Associate to conduct and coordinate clinical monitoring and site management for oncology trials. The role focuses on regulatory compliance, data reliability, investigator-site collaboration, and trial progress from site initiation through closeout. Tags Health Care Life Science Pharmaceutical Artificial Intelligence (AI) Accounting Human Resources He

The hiring company is not identified in the posting. The role performs and coordinates clinical monitoring and site management, including remote or on-site visits to assess protocol and regulatory compliance, manage documentation, ensure audit readiness, and build collaborative relationships with investigational sites. Tags Health Care Life Science Pharmaceutical Artificial Intelligence (AI) Accounting Human Resource

Fortrea is seeking Clinical Trial Managers to oversee clinical delivery and operational activities for clinical research trials. The role collaborates with project managers and functional leads to deliver clinical and start-up activities within budget and contract while ensuring quality, compliance, and country-specific commitments. Responsibilities End-to-end oversight of start-up and clinical responsibilities—from

BeOne is a growing company focused on fighting cancer and developing affordable medicines. The Regional Clinical Trial Management Associate supports regional and country-level clinical study delivery, study start-up, trial operations, quality, timelines, documentation, stakeholder collaboration, and budget activities under the guidance of the Regional Clinical Study Manager. Responsibilities Supports the Regional Cli

Fortrea is a global contract research organization providing clinical development, patient access, and technology solutions across multiple therapeutic areas. The Project Coordinator I will support Phase I clinical trials by coordinating study activities, maintaining documentation, tracking timelines, managing clinical systems, and collaborating with internal teams, external sites, and vendors. Tags Health Care Life

Worldwide Clinical Trials is a global contract research organization focused on advancing clinical research and improving patient lives. The Clinical Research Associate II will manage research activities at clinical trial sites across all study stages, including site identification, study start-up, training, maintenance, compliance, and closeout, with a focus on cardiology or hypertension studies. Tags Health Care Li

Fortrea is hiring Clinical Research Associates through its Monitoring Excellence Academy for oncology, CAR T, and ophthalmology clinical trials. The role monitors and manages study sites, protects participants, ensures protocol and regulatory compliance, reviews clinical data, and supports clinical project coordination while requiring substantial travel. Tags Health Care Life Science Pharmaceutical Artificial Intelli

Cedar Gate Technologies, an IQVIA business, provides healthcare technology and services for value-based care. The Healthcare Analytics, AI Product & Methodology Analyst will help evaluate and develop AI-enabled healthcare analytics solutions, define analytical requirements, validate AI-generated outputs, and assess methodology changes affecting provider performance insights. The role collaborates with product, analyt

The company is a global clinical research organization supporting pharmaceutical and biotechnology companies with clinical trials worldwide. The Clinical Research Associate II will perform and coordinate clinical monitoring and site management activities, ensuring protocol, regulatory, ICH-GCP, and SOP compliance while maintaining data quality and audit readiness. Tags Health Care Life Science Pharmaceutical Artifici

Thermo Fisher Scientific is a global scientific organization committed to innovation and scientific excellence. The Clinical Study Planning & Scheduling Lead owns integrated study calendars across clinical research units, evaluates study placement and scheduling needs, coordinates cross-functional planning, and supports capacity planning and Human Safety Committee activities. Responsibilities Owns and maintains the i

Veeva Systems is a mission-driven SaaS company focused on helping life sciences companies bring therapies to patients faster. The Product Manager will drive features and enhancements for the Vault Clinical Operations suite, manage the product lifecycle and backlog, gather requirements, and collaborate with cross-functional teams to improve clinical trial execution. Tags Health Care Life Science Pharmaceutical Artific

Syneos Health is a global company focused on creating better, smarter, and faster ways to bring biopharmaceutical therapies to patients. The Compliance Specialist will support REMS Call Center programs by investigating, documenting, and addressing potential noncompliance, coordinating corrective actions, providing stakeholder training, and participating in auditing and monitoring activities. Tags Health Care Life Sci

Lifelancer is a talent-hiring platform serving the life sciences, pharmaceutical, healthcare, health technology, and IT sectors. The Clinical Trial Coordinator provides administrative and technical support to project teams, supporting audit readiness, site activation, feasibility activities, regulatory submissions, documentation management, and clinical trial systems. The role also coordinates site communications, tr

Lifelancer is a talent-hiring platform connecting professionals with opportunities in life sciences, pharma, health sciences, healthtech, and IT. This role supports clinical trial monitoring and site management for Alzheimer’s studies, ensuring protocol, regulatory, and ICH-GCP compliance, data reliability, audit readiness, and effective communication with investigative sites and project teams. Responsibilities Monit

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The Remote Visit Coordinator, US Regional Specialist supports remote and decentralized trial visit execution by coordinating sites, research clinicians, documentation, systems, logistics, and communications across assigned studies. Responsibilities Conduct outreach and training

IQVIA Biotech is a full-service contract research organization serving biotech sponsors with clinical research solutions. The Clinical Trial Manager II or Senior Clinical Trial Manager will lead complex global clinical trials, oversee clinical delivery and quality, drive recruitment, manage risks and project resources, and guide international cross-functional teams from startup through closeout. Tags Health Care Life

Lifelancer is a talent-hiring platform serving the life sciences, pharmaceutical, and IT sectors. The FSP Country Approval Specialist supports the preparation, review, coordination, and management of local regulatory and ethics submissions for clinical trials. The role also coordinates site start-up activities, maintains study documentation and tracking databases, and provides country-level submission support. Respon