Senior CRA- Remote - Blue Bell, PA

Job summary · Clinical Research Associate (Senior CRA) ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical Research Associate (CRA) to join our dynamic, collaborative team. · ResponsibilitiesConducting site qualification, initiation, mon ...

CRA II or Senior CRA-US-Remote · 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 ...

+We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. · +Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. · Ensuring protocol compliance, data integrit ...

The Clinical Trial Manager / Senior Clinical Trial Manager will oversee the clinical portion of the budget to ensure efficient resource allocation. · ...

Sr. Clinical Research AssociateICON 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 de ...

Senior CRA- Remote · 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 ...

Job Description · This role is accountable for the execution and oversight of local operational start up clinical trial activities in compliance with ICH/GCP and US regulations. This position will have end to end accountability of US Site and Study Start Up as well as develop new ...

Job Description · This role is accountable for the execution and oversight of local operational start up clinical trial activities in compliance with ICH/GCP and US regulations. This position will have end to end accountability of US Site and Study Start Up as well as develop new ...

The Scientist will support clinical/scientific activities on single studies or across multiple studies. They will develop protocol-related study materials and interact with internal/external stakeholders. · ...

Responsible for specific clinical/scientific activities on a single study or across multi studies (e.g., medical monitoring, lab specimen tracking/reconciliation, · adjudication support, preparation of meeting materials). Support development of Protocol and related study material ...

Responsible for specific clinical/scientific activities on a single study or across multi e studies. · Support development of Protocol and related study materials.May interact with internal and external stakeholders in support of clinical study objectives.Cross-functionally to mo ...

Job Description · This role is accountable for the execution and oversight of local operational start up clinical trial activities in compliance with ICH/GCP and US regulations. This position will have end to end accountability of US Site and Study Start Up as well as develop new ...

The job involves specific clinical/scientific activities on a single study or across multiple studies. The successful candidate will be responsible for medical monitoring, lab specimen tracking/reconciliation, adjudication support, and preparation of meeting materials. · ...

ClinChoice is seeking an experienced Freelance Clinical Research Associate (CRA) to monitor a Phase I oncology trial. This is a full-time (1.0 FTE), remote position for a U.S.-based CRA, with approximately 70% travel to investigative sites. Opened to 1099 independent contractors. ...

ClinChoice is seeking an experienced Freelance Clinical Research Associate (CRA) to monitor a Phase I oncology trial. This is a full-time (1.0 FTE), remote position for a U.S.-based CRA, with approximately 70% travel to investigative sites. Opened to 1099 independent contractors. ...

Job Summary: Perform the clinical monitoring aspect of designated projects in accordance with study specific procedures, applicable SOPs, and regulations. Act as direct contact with assigned CRA and use judgment to assess and ensure overall integrity of study implementation and a ...

This role within GCSD plays a pivotal part in driving the clinical operations of assigned studies. The Global Study Manager will take ownership of crafting robust delivery plans that aim for top-tier performance. · GSM will be the Working Group (WG) Lead for Clinical Operations w ...

This role within GCSD plays a pivotal part in driving clinical operations of assigned studies from Commit to Study Initiation (CSI) all the way through study archiving As Global Study Manager (GSM) you'll craft robust accelerated delivery plans ensuring timelines quality standard ...

The Clinical Operations Manager will lead operational execution of assigned clinical trials under both in-house managed models and outsourced models. · Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field (required) · ...

We are seeking a Clinical Operations leader to drive execution across pain-focused clinical trials. The successful candidate will oversee CRAs and site performance ensuring timelines quality patient safety and inspection readiness. · Own end-to-end operational delivery for assign ...