Oncology - CAR-T - CRA II - Remote US - Durham - Fortrea

We are currently seeking experienced Cardiology Device or Electrophysiology Sr.CRAs with 5+ years of monitoring experience to join our FSP team Experience in Cardio Device is required for this role. · ...

We are currently seeking experienced Cardiology Device or Electrophysiology Sr. CRAs with 5+ years of monitoring experience to join our FSP teamThe Senior CRA II is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/ ...

We are currently seeking experienced Cardiology Device or Electrophysiology Sr. CRAs with 5+ years of monitoring experience to join our FSP team. · Responsibilities:Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely ...

We are seeking experienced Cardiology Device or Electrophysiology Sr. CRAs for our FSP team with responsibility for clinical studies according to Fortrea. · The Senior CRA II will be responsible for site monitoring and management under the direction of a Project Manager/Director. ...

We are currently seeking experienced Cardiology Device or Electrophysiology Sr. CRAs with 3+ years of monitoring experience to join our FSP team. · Experience in Cardiology, Device or Electrophysiology is required for this role. · ...

We are currently seeking experienced Cardiology Device or Electrophysiology Sr. CRAs with 3+ years of monitoring experience to join our FSP team Experience in Cardiology, Device or Electrophysiology is required for this role This role will include some nationwide travel during st ...

Job Title: · Clinical Trial Assistant · The Clinical Trial Assistant plays a crucial role in supporting the Clinical Operations team by managing essential documents in the TMF, · developing study materials, and coordinating shipments of clinical trial materials. · This role invol ...

The Clinical Trial Assistant plays a crucial role in supporting the Clinical Operations team by managing essential documents in the TMF, developing study materials and coordinating shipments of clinical trial materials. · Assist in the development handling distribution filing and ...

The Clinical Trial Assistant plays a crucial role in supporting the Clinical Operations team by managing essential documents in the TMF, developing study materials, · and coordinating shipments of clinical trial materials. · Assist in the development, handling, distribution, fili ...

+Job summary · The Clinical Trial Assistant plays a crucial role in supporting the Clinical Operations team by managing essential documents in the TMF, developing study materials, and coordinating shipments of clinical trial materials.Assist in the development, handling, distribu ...

The Clinical Research Associate will collaborate closely with investigative study sites to complete required site visits and perform site management activities. The CRA must build and maintain strong collaborative relationships with investigative sites, as well as leverage strong ...

The Clinical Research Associate will collaborate closely with investigative study sites to complete required site visits and perform site management activities. · The CRA must build and maintain strong collaborative relationships with investigative sites and leverage strong knowl ...

We are currently seeking Sr CRAs with 4+ years of monitoring within in United States. Travel is expected to be regional as well as to Puerto Rico (seeking a candidate with direct flight to PR) and about 50% overnight. · Job Overview: · The Senior CRA 2 is responsible for site mon ...

We are currently seeking Sr CRAs with 4+ years of monitoring within in United States. Travel is expected to be regional and about 50% overnight. · Job Overview: · The Senior CRA 2 is responsible for site monitoring and site management. Responsibility for clinical studies accordin ...

+This fully remote role is responsible for managing multiple clinical trial sites from study start-up through closeout,+ · +Guide site personnel through all aspects of study readiness,+ · Maintain real-time updates in the CTMS and log daily site communications,+ · ...

This fully remote role is responsible for managing multiple clinical trial sites from study start-up through closeout. · ...

This fully remote role is responsible for managing multiple clinical trial sites from study start-up through closeout. · ...

This fully remote role is responsible for managing multiple clinical trial sites from study start-up through closeout. The Clinical Trial Coordinator will ensure all essential documents are collected, reviewed, approved and filed correctly to support rapid site activation. · The ...

+Job summary · This fully remote role is responsible for managing multiple clinical trial sites from study start-up through close-out. · +ResponsibilitiesGuide site personnel through all aspects of study readiness. · Maintain real-time updates in the CTMS and log daily site commu ...

This fully remote role is responsible for managing multiple clinical trial sites from study start-up through closeout. The Clinical Trial Coordinator will ensure all essential documents are collected and reviewed correctly to support rapid site activation. · ...