中国 的 Fortrea 职位

Clinical Team Leads (CTL) own the clinical delivery of clinical research trials.The CTL oversees the clinical and site management aspects of the trial. · Take accountability for proactively driving clinical project performance toward contracted deliverables while meeting customer ...

The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. · ...

The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. · Diploma – Associate degree or equivalent. · In lieu of the above requirement, candidates with 1-2 or more years of relevant Cli ...

The candidate will assist with clinical safety and post-marketing surveillance operations for products including adverse event data from clinical trials and unsolicited reports. · Process Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs) · ...

This position is for a Clinical Trial Administrator (CTA) who will perform study-related tasks as required by the department. The CTA will communicate with project team members, maintain documentation, and provide systems support. · Document and track study activities. · Assist i ...

Site management responsibility for clinical studies according to Fortrea's Standard Operating Procedures, · ICH GCP Guidelines, applicable project plans and Sponsor requirements, · including verification of study training records. · ...

The Senior Business Development Director achieves annual sales plan and sales targets for assigned accounts through proactive sales activity and networking with assigned potential and existing accounts.Achieves annual sales plan and sales targets for assigned accounts through pro ...

+ Site monitoring and site management responsibility for clinical studies according to Company standard operating procedures + Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites + General On-Site Monitoring Responsibil ...

FSP CRA II is responsible for Description of Responsibilities · A list of all the responsabilities of a FSP CRA II., · The list of pre requisites for this position ...

The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. · ...

The Regulatory Coordinator will be responsible for primary contact with investigative sites during study maintenance and site startup activities. · ...

This role is for upcoming future opportunities that may arise at Fortrea. · Site management responsibility for clinical studies according to Fortrea's Standard Operating Procedures. · Conducts site monitoring responsibilities for clinical trials. · ...

The Clinical Research Associate II conducts site management responsibility for clinical studies and site monitoring responsibilities for clinical trials according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements. · ...

The Clinical Trials Coordinator will be responsible for primary contact with investigative sites during site start-up activities and maintenance. They will collect required investigator and essential documents to ensure EC/IRB/Third body/Regulatory Authority applications are made ...

This role is for upcoming future opportunities that may arise at Fortrea. Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. ...

Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. · ...

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, · Sponsor Regulatory Guidelines. Assures the implementation of project plans. · ...

Site monitoring responsibility for clinical studies according to Company Standard Operating Procedures, · Sponsor Standard Operating Procedures. · Assures the implementation of project plans as assigned. · ...

Site monitoring and site management responsibility for clinical studies according to Company Standard Operating Procedures Regulatory Guidelines. · ...

The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. · ...