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. · ...

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

Job Overview · Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. · Summary Of Responsibilities · Respons ...

The Core CRA II is responsible for site management and clinical monitoring activities according to Fortrea's Standard Operating Procedures and ICH GCP Guidelines. · ...

The Clinical Research Associate (CRA) is responsible for site management of clinical studies according to Fortrea's Standard Operating Procedures and ICH GCP Guidelines. The CRA conducts site monitoring responsibilities including Pre-study, Site Initiation, Process Monitoring, Ro ...

Job Overview · Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. · Summary Of Responsibilities · Respons ...

The Senior Business Development Director achieves annual sales plans and targets through proactive sales activity and networking. Establishes client relationships at appropriate levels. · ...

Job Overview · Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study, to ensure EC/IRB/Third body/Regulatory Authority and any other local appl ...

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know when the role officially opens, so we can reconfirm you ...

This role is for upcoming future opportunities that may arise at Fortrea. · Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview.If you're pre-selected, our recruiter will keep in tou ...

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 ...

The Senior CRA I is responsible for site monitoring and site management. The job involves ensuring the study staff who will conduct the protocol have received proper materials and instructions to safely enter patients into the study. · ...

Lead writer independently responsible for the preparation of clinical study protocols and clinical study reports (CSRs), and other documents as needed for lower complexity studies. · ...

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

The TMF Reviewer III manages electronic Trial Master Files (eTMF) for clinical studies in support of sponsor services contracts and internal business needs. · ...

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. · Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sit ...

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 ...

Fortrea is excited to connect with talented individuals for future opportunities. · ...

Responsibility for clinical studies according to Company Standard Operating Procedures and Regulatory Guidelines. · ...