FTITA Fortrea Development Limited Filiale Italiana

*** Multiple night shifts available as follows******Free parking onsite just steps away from the clinic***Straight Night Shift / Weekdays Only: (12 Hour) 6 PM 6 AMStraight Night Shift / Weekdays Only: (8 Hour) 11 PM 7 AMStraight Night Shift / Weekends Only: (12 Hour) 6 PM 6 AMAs on

*** Multiple night shifts available as follows******Free parking onsite just steps away from the clinic***Straight Night Shift / Weekdays Only: (12 Hour) 6 PM 6 AMStraight Night Shift / Weekdays Only: (8 Hour) 11 PM 7 AMStraight Night Shift / Weekends Only: (12 Hour) 6 PM 6 AMAs on

*** Free parking ***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a RNs LPNs and Paramedics to interact directly with our healthy volunteer participants while learning to

*** Free parking ***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a RNs LPNs and Paramedics to interact directly with our healthy volunteer participants while learning to

Job Overview:The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their experience and level of contribution which they can mak

Job Overview:The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their experience and level of contribution which they can mak

As a Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex projects for a renowned innovative and global top pharmaceutical company.You will be involved in liaising with the entire study team as

As a Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex projects for a renowned innovative and global top pharmaceutical company.You will be involved in liaising with the entire study team as

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

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 applications

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 applications

Job Overview:Accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local financial compliance at a country operations level at the client. The position has a significant impact on how a country can deliver coun

Job Overview:Accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local financial compliance at a country operations level at the client. The position has a significant impact on how a country can deliver coun

Summary of Responsibilities:Perform contract management tasks on medium complexity projects as assigned.Serve as contract management lead for strategic accounts as assigned.Independently develop and review Agreements including Master Services Agreements (Fortrea multi-unit single unit

Summary of Responsibilities:Perform contract management tasks on medium complexity projects as assigned.Serve as contract management lead for strategic accounts as assigned.Independently develop and review Agreements including Master Services Agreements (Fortrea multi-unit single unit

Job Overview:Perform and coordinate a variety of tasks to support the company as part of the leadership of the office service team.Summary of Responsibilities:Order office supplies for firm; perform associated administrative tasks including coding and assembling of invoice packages fo

Job Overview:Perform and coordinate a variety of tasks to support the company as part of the leadership of the office service team.Summary of Responsibilities:Order office supplies for firm; perform associated administrative tasks including coding and assembling of invoice packages fo

Summary of Responsibilities:Owns all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) for assigned opportunities (inclusive of managing opportunities under general supervision establishing clear timelines meeting client r

Summary of Responsibilities:Owns all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) for assigned opportunities (inclusive of managing opportunities under general supervision establishing clear timelines meeting client r

Regulatory Affairs Specialist Global Submissions & Quality DocumentationJoin Fortreas dynamic global team supporting pharmaceutical product development and lifecycle this role youll be responsible for preparing reviewing and managing regulatory and quality documentation for submissi

Regulatory Affairs Specialist Global Submissions & Quality DocumentationJoin Fortreas dynamic global team supporting pharmaceutical product development and lifecycle this role youll be responsible for preparing reviewing and managing regulatory and quality documentation for submissi

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process ex

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process ex

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process expendable

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process expendable

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar

Job Overview: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. The Senior CRA I assure the implementation of project plans as assigne

Job Overview: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. The Senior CRA I assure the implementation of project plans as assigne

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Job Overview: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. The Senior CRA I assure the implementation of project plans as assigne

Job Overview: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. The Senior CRA I assure the implementation of project plans as assigne

We are currently seeking experienced Oncology CRAs residing in the West (Northern CA NV AZ ID NM OR WA or CO). Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operati

We are currently seeking experienced Oncology CRAs residing in the West (Northern CA NV AZ ID NM OR WA or CO). Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operati

Fortreas FSP team is hiring experienced Sr. Project Coordinators with prior CRO experience! 3 years of PC experience preferred. Oncology experience highly desired. Ability to work some West Coast hours is ideal. Job Overview:Coordinates the activities associated with the evaluation in

Fortreas FSP team is hiring experienced Sr. Project Coordinators with prior CRO experience! 3 years of PC experience preferred. Oncology experience highly desired. Ability to work some West Coast hours is ideal. Job Overview:Coordinates the activities associated with the evaluation in