Fortrea

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 well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let

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 well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let

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: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. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica

Job Overview: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. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica

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 exp

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 exp

Our FSO team is seeking a Cardiology Respiratory Diabetes/Weight loss Immunology or MASH Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience. Candidates must be based in the United States. J

Our FSO team is seeking a Cardiology Respiratory Diabetes/Weight loss Immunology or MASH Sr. Clinical Project Manager or Project Manager II to join our growing team. This role requires 3-5 years of global project management experience. Candidates must be based in the United States. J

Be the connection between science and solutions. As a Clinical Research Associate II you will take the next step in your clinical research career supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals w

Be the connection between science and solutions. As a Clinical Research Associate II you will take the next step in your clinical research career supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals w

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:Responsible for all asp

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:Responsible for all asp

Job Overview:The Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE they are expected to leverage their leadership competencies clinical delivery execution experience and client relationships to drive both financial

Job Overview:The Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE they are expected to leverage their leadership competencies clinical delivery execution experience and client relationships to drive both financial

Job Overview: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. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica

Job Overview: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. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinica

Job Overview:Our FSO team is seeking anCell & Gene Therapy Sr. Clinical Project Manager or Project Manager IIto join our growing team. This role requires 3-5 years of global project management experience withmandatory experience in cell & gene Therapy. Candidates must bebased in the l

Job Overview:Our FSO team is seeking anCell & Gene Therapy Sr. Clinical Project Manager or Project Manager IIto join our growing team. This role requires 3-5 years of global project management experience withmandatory experience in cell & gene Therapy. Candidates must bebased in the l

Job Overview:The Clinical Research Associate I MEA (CRA I MEA) 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 CRA I MEA shall reflect their experience and level of contribution w

Job Overview:The Clinical Research Associate I MEA (CRA I MEA) 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 CRA I MEA shall reflect their experience and level of contribution w

Job Overview:The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job.Summary of Responsibilities:Achieves annual sales plan and sales targets for assigned accou

Job Overview:The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job.Summary of Responsibilities:Achieves annual sales plan and sales targets for assigned accou

Job Overview:The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job.Summary of Responsibilities:Achieves annual sales plan and sales targets for assigned accou

Job Overview:The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job.Summary of Responsibilities:Achieves annual sales plan and sales targets for assigned accou

The Executive Director Clinical Platforms & Product Development is a senior technology and operations leader responsible for defining building and operationalizing Fortreas Clinical Platforms ecosystem. This role serves as the strategic and operational partner to the Vice President Cl

The Executive Director Clinical Platforms & Product Development is a senior technology and operations leader responsible for defining building and operationalizing Fortreas Clinical Platforms ecosystem. This role serves as the strategic and operational partner to the Vice President Cl

The Executive Director Clinical Platforms & Product Development is a senior technology and operations leader responsible for defining building and operationalizing Fortreas Clinical Platforms ecosystem. This role serves as the strategic and operational partner to the Vice President Cl

The Executive Director Clinical Platforms & Product Development is a senior technology and operations leader responsible for defining building and operationalizing Fortreas Clinical Platforms ecosystem. This role serves as the strategic and operational partner to the Vice President Cl

Job Overview:The Senior Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE they are expected to leverage their leadership competencies clinical delivery execution experience and client relationships to drive both fi

Job Overview:The Senior Director level of Clinical Delivery Center of Excellence (CoE) is an experienced leader within the Clinical Delivery CoE they are expected to leverage their leadership competencies clinical delivery execution experience and client relationships to drive both fi

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation system set-up data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study star

We are looking to hire a Clinical Team Lead (Local Trial Manager) in France. In this position you will be fully dedicated to a single sponsor. This position is open for full-time candidates.Responsibilities/Provide end-to-end operational oversight for the assigned study(ies) including

We are looking to hire a Clinical Team Lead (Local Trial Manager) in France. In this position you will be fully dedicated to a single sponsor. This position is open for full-time candidates.Responsibilities/Provide end-to-end operational oversight for the assigned study(ies) including

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: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