Are you passionate about clinical research and regulatory excellence Fortrea is seeking a Start Up Country Lead to join our team in France. This role offers a unique opportunity to lead regulatory operations for clinical trials ensuring compliance quality and timely delivery of study

Are you passionate about clinical research and regulatory excellence Fortrea is seeking a Start Up Country Lead to join our team in France. This role offers a unique opportunity to lead regulatory operations for clinical trials ensuring compliance quality and timely delivery of study

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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

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Job Overview:Responsible for assisting with 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

Job Overview:Responsible for assisting with 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

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Job Overview:The Global Feasibility Lead 2 will play an integral role in operational strategy and planning in the preaward space through participation in strategy development conversations robust primary and secondary data collection and analysis and development of feasibility and sit

Job Overview:The Global Feasibility Lead 2 will play an integral role in operational strategy and planning in the preaward space through participation in strategy development conversations robust primary and secondary data collection and analysis and development of feasibility and sit

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Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confide

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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 you know when the role officially opens so we can reconfirm your interest

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 you know when the role officially opens so we can reconfirm your interest

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We are looking to bring an experienced Centralized Study Specialist to our team in Bulgaria.Responsibilities will include:Review initial/amended Country/Site ICFs in compliance with Sponsor requirements local regulatory requirements and Good Clinical Practice (GCP) guidelinesReview an

We are looking to bring an experienced Centralized Study Specialist to our team in Bulgaria.Responsibilities will include:Review initial/amended Country/Site ICFs in compliance with Sponsor requirements local regulatory requirements and Good Clinical Practice (GCP) guidelinesReview an

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Shape the Future of Data at FortreaAre you a visionary leader in data architecture and integration Fortrea is seeking a Chief Data Officer to drive the strategy and execution of services that will deliver the future state for Fortreas global data platforms.The role will require the de

Shape the Future of Data at FortreaAre you a visionary leader in data architecture and integration Fortrea is seeking a Chief Data Officer to drive the strategy and execution of services that will deliver the future state for Fortreas global data platforms.The role will require the de

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As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology sol

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As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were looking for a Clinical Pharmacist to play a key role in supporting clinical trials and ensuring the safe and compliant handling of investigational

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were looking for a Clinical Pharmacist to play a key role in supporting clinical trials and ensuring the safe and compliant handling of investigational

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As aProposal Manager IIwithin Fortreas Enterprise Client Solutions team youll play a pivotal role in driving the proposal process for opportunities including RFIs and RFPs. This position is ideal for someone who thrives in a fast-paced matrixed environment and enjoys collaborating acr

As aProposal Manager IIwithin Fortreas Enterprise Client Solutions team youll play a pivotal role in driving the proposal process for opportunities including RFIs and RFPs. This position is ideal for someone who thrives in a fast-paced matrixed environment and enjoys collaborating acr

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Are you detail-oriented and passionate about supporting clinical research operations Join our team in Paris as Project Assistant with Budget and Contract skills where youll play a key role in enabling regulatory or financial workflows across clinical studies. This is a sponsor-dedicat

Are you detail-oriented and passionate about supporting clinical research operations Join our team in Paris as Project Assistant with Budget and Contract skills where youll play a key role in enabling regulatory or financial workflows across clinical studies. This is a sponsor-dedicat

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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 seeking a Clinical Research Pharmacist II who will play a critical role in supporting clinical trials by ensuring the safe and compliant preparat

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 seeking a Clinical Research Pharmacist II who will play a critical role in supporting clinical trials by ensuring the safe and compliant preparat

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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

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***Must have at least 1 year of experience working within a clinical research role***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 Study Coordinator II to interact direct

***Must have at least 1 year of experience working within a clinical research role***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 Study Coordinator II to interact direct

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Assists Proposal Managers with all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) (i.e. collating data following up with other departments meeting minutes etc.).Responsible for managing opportunities of low complexity w

Assists Proposal Managers with all aspects of the appropriate proposal process (text quote budget and/or response to Requests for Information RFIs) (i.e. collating data following up with other departments meeting minutes etc.).Responsible for managing opportunities of low complexity w

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Summary of Responsibilities:Follow applicable departmental Standard Operating Procedures and Work Instructions.Complete required trainings according to required timelines.Administer controlled documents ensuring availability to the end user.Track and report metrics as determined by ma

Summary of Responsibilities:Follow applicable departmental Standard Operating Procedures and Work Instructions.Complete required trainings according to required timelines.Administer controlled documents ensuring availability to the end user.Track and report metrics as determined by ma

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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

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Join Our Product Management Team at Fortrea! Were seeking a Product Manager with deep industry expertise and proven experience in Risk-Based Quality Management (RBQM) to lead the development of data-driven solutions that drive innovation in life sciences.In this role youll define str

Join Our Product Management Team at Fortrea! Were seeking a Product Manager with deep industry expertise and proven experience in Risk-Based Quality Management (RBQM) to lead the development of data-driven solutions that drive innovation in life sciences.In this role youll define str

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As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were looking for a Clinical Pharmacist to play a key role in supporting clinical trials and ensuring the safe and compliant handling of investigational

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.Were looking for a Clinical Pharmacist to play a key role in supporting clinical trials and ensuring the safe and compliant handling of investigational

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