clinical research associate remote

CamWebDir in Rahway, NJ seeks an experienced Clinical Research Site Manager to oversee performance and compliance for assigned protocols and sites. The role ensures study conduct aligns with ICH/GCP, country regulations, and company policies while maintaining site relationships and overall study readiness. The candidate will travel up to 65-75%...

Precision Medicine Group is expanding capabilities across Latin America and is hiring a Senior Clinical Research Associate to support critical studies in Argentina and beyond. The Senior CRA will manage site start-up, monitoring, regulatory submissions, and provide mentorship to junior staff while ensuring high-quality data and patient safety. Expect up to...

Syneos Health is seeking a Clinical Research Associate to join our Austria site. The role involves on-site or remote monitoring, site qualification, initiation, and management activities while ensuring regulatory and protocol compliance. You will verify informed consent, protect patient data, and drive data integrity. Required are a Bachelor’s degree or...

Precision for Medicine is seeking Senior Clinical Research Associates in Poland, Hungary, United Kingdom, France and Germany to support a dedicated FSP partnership, with a fully home-based role within France. You will monitor clinical studies at investigative sites, ensure conduct per protocol, SOPs, ICH-GCP, and regulatory standards, and coordinate site...

Precision for Medicine seeks a Senior Clinical Research Associate to support a dedicated FSP partnership across Poland, Hungary, the United Kingdom, France, and Germany. The role offers a fully home-based arrangement within Germany for eligible candidates and involves collaboration with sponsor teams in a quality-focused environment. Candidates should have...

Orca Bio is seeking a Clinical Research Associate for remote US roles, with travel to sites as needed. You will monitor clinical studies, ensure compliance with SOPs and ICH-GCP, and support site staff across multiple locations. You will conduct IMVs/ISF reviews, verify data with SDV/EMR, and contribute to trial material development and SOP creation to...

Fortrea is seeking a Clinical Research Associate with 1+ years of experience to monitor Phase I studies. The role focuses on site monitoring, data integrity, and regulatory compliance, with significant travel to sites. The candidate should reside in Florida and be comfortable with a fast-paced, team-oriented environment. Responsibilities include site...

Ethos is seeking experienced clinical research associates to help train an AI language model using professional documents, spreadsheets, and slide decks. This fully remote engagement offers flexible hours and compensation at $100 per hour. Candidates should have 5+ years in clinical research or related fields, with deep familiarity with ICH-GCP, FDA/EMA...

Job Description The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and...

Syneos Health is seeking a CRA II in Germany to perform site qualification, initiation, on-site or remote monitoring, and close-out visits, ensuring adherence to ICH-GCP and regulatory standards. You will coordinate with trial sites across the DACH region and manage data quality and safety documentation. The role requires fluency in German and English, a...

Parexel is seeking a Clinical Monitor to oversee monitoring responsibilities and study conduct across sites, ensuring regulatory, ICH-GCP and protocol compliance, and timely issue escalation. You will perform source verification, IP accountability, data integrity checks, and collaborate with site staff and the global team, with emphasis on patient safety...

Job Description The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and...

Job Description The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and...

Job Description The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and...

Job Description The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and...

Job DescriptionThe role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations,our Companypolicies and procedures, quality standards and adverse event reporting requirements internally and...

Job Description The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and...

Job Description The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and...

Job Description The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and...

Job Description The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and...