Clinical Trial Specialist

Job Title: Monitoring Specialist About the Job: The role of a monitoring specialist is to ensure that clinical trials are conducted in accordance with Good Clinical Practice (GCP) guidelines and regulatory requirements. This involves conducting on-site visits to monitor investigator sites, identifying potential issues, and taking corrective actions.

Job Description:As a Clinical Research Associate (CRA), you will play a pivotal role in ensuring the integrity and compliance of clinical trials. You will be responsible for monitoring investigator sites, identifying potential issues, and implementing corrective actions to ensure trial success.Required Skills and Qualifications:

**Clinical Project Manager****(Level Depends on Experience)****Job Purpose/Summary**: Responsible for management and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client’s goals of time, budget and quality performance are met. The Clinical Project Manager I is expected to require support and guidance from Directors and/or...

Clinical Project Manager – Level Dependent on Experience CTI Clinical Trial and Consulting Services is a global, privately held, full‑service clinical contract research organization focused on advancing treatments for chronically and critically ill patients. We support clinical research throughout the life cycle of development, from drug concept to...

Job Description:As a Clinical Research Associate (CRA), you will play a pivotal role in ensuring the integrity and compliance of clinical trials. You will be responsible for monitoring investigator sites, identifying potential issues, and implementing corrective actions to ensure trial success.Required Skills and Qualifications:Strong analytical and...

Job Description: As a Clinical Research Associate (CRA), you will play a pivotal role in ensuring the integrity and compliance of clinical trials. You will be responsible for monitoring investigator sites, identifying potential issues, and implementing corrective actions to ensure trial success. Required Skills and Qualifications: Strong analytical and...

Job Description: As a Clinical Research Associate (CRA), you will play a pivotal role in ensuring the integrity and compliance of clinical trials. You will be responsible for monitoring investigator sites, identifying potential issues, and implementing corrective actions to ensure trial success. Required Skills and Qualifications: Strong analytical and...

Clinical Trials Project Coordinator We are seeking a skilled Clinical Trials Project Coordinator to join our team and support the planning, coordination, and execution of clinical trials. The ideal candidate will have previous experience in clinical trial monitoring and a solid understanding of Good Clinical Practice (GCP) principles. About the Role: This is...

Clinical Trial Manager - Sao Paulo, Brazil (Homebased) 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. Role: Clinical Trial Manager Location:...

Job Role: Clinical Research Associate - Site Management Job Description: This role involves site monitoring and management for clinical trials. The Clinical Research Associate (CRA) will be responsible for ensuring compliance with the protocol, regulatory requirements, and Good Clinical Practice (GCP). This includes conducting on-site visits to monitor...