Fortrea

Join Fortreas Medical Device & Diagnostics team and make a difference as Lead Data Manager!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

Join Fortreas Medical Device & Diagnostics team and make a difference as Lead Data Manager!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

Join Fortreas Medical Device and Diagnostics team and make a difference as Clinical Data Analyst!Job Overview:Serve as a member of the project team with primary responsibility for coordinating the clinical data review query generation / resolution and reconciliation activities to supp

Join Fortreas Medical Device and Diagnostics team and make a difference as Clinical Data Analyst!Job Overview:Serve as a member of the project team with primary responsibility for coordinating the clinical data review query generation / resolution and reconciliation activities to supp

Join our Proposal Management team as a Proposal Manager I where youll play a key role in bringing new business opportunities to life. Youll manage the end-to-end proposal processworking across teams to develop tailored high-quality responses to client requests including budgets timeli

Join our Proposal Management team as a Proposal Manager I where youll play a key role in bringing new business opportunities to life. Youll manage the end-to-end proposal processworking across teams to develop tailored high-quality responses to client requests including budgets timeli

IT Program Manager Lead Global Transformation Fully Remote Fixed Term (12 months)Are you ready to lead high-impact global technology programmes that shape the future of digital delivery in a regulated environmentWere looking for an experienced IT Program Manager to take ownership of

IT Program Manager Lead Global Transformation Fully Remote Fixed Term (12 months)Are you ready to lead high-impact global technology programmes that shape the future of digital delivery in a regulated environmentWere looking for an experienced IT Program Manager to take ownership of

Join one of the worlds largest Clinical Research Organizations and play a key role in advancing new medical treatments. Our Early Phase Unit is seeking a Lab Technician to support healthy volunteer clinical trials and help generate highquality data that shapes the future of medicine.T

Join one of the worlds largest Clinical Research Organizations and play a key role in advancing new medical treatments. Our Early Phase Unit is seeking a Lab Technician to support healthy volunteer clinical trials and help generate highquality data that shapes the future of medicine.T

Senior Site NavigatorJob Code: 700344 Job Level: P2 Individual Contributor Function: Clinical Operations Work Model: Remote / Office-based with travel as neededAbout the RoleAs a Senior Site Navigator youll act as a local country or regional expert in study start-up leading site-leve

Senior Site NavigatorJob Code: 700344 Job Level: P2 Individual Contributor Function: Clinical Operations Work Model: Remote / Office-based with travel as neededAbout the RoleAs a Senior Site Navigator youll act as a local country or regional expert in study start-up leading site-leve

Job Overview:The Senior Director level of Strategic Delivery and Growth (SDG) is an experienced leader within SDG they are expected to leverage their leadership competencies research and development experience Therapeutic Area (TA) experience and operational study execution experience

Job Overview:The Senior Director level of Strategic Delivery and Growth (SDG) is an experienced leader within SDG they are expected to leverage their leadership competencies research and development experience Therapeutic Area (TA) experience and operational study execution experience

Our Phase I team is currently seeking a Sr. Clinical Project Manager with 4 years of project management experience residing in Canada. Ideal candidates would have phase Ib experience. Job Overview:Primary client contact for assigned clinical studies or programs working independently w

Our Phase I team is currently seeking a Sr. Clinical Project Manager with 4 years of project management experience residing in Canada. Ideal candidates would have phase Ib experience. Job Overview:Primary client contact for assigned clinical studies or programs working independently w

Summary of Responsibilities:Work with PA to generate cover letter or Proforma invoice and payment batch generation in CTMS.Review EDC Contract and mark line items Ready to Pay/Screen Failure in CTMSPerform Invoice QC and Prepare GIA as applicable.Coordinate with CTL PM for line-item a

Summary of Responsibilities:Work with PA to generate cover letter or Proforma invoice and payment batch generation in CTMS.Review EDC Contract and mark line items Ready to Pay/Screen Failure in CTMSPerform Invoice QC and Prepare GIA as applicable.Coordinate with CTL PM for line-item a

About the RoleThis unique hybrid role blends the responsibilities of site startup site navigation and clinical monitoring. As a SCRA / Site Navigator II you will serve as a trusted partner to investigative sites across the full study lifecyclefrom feasibility and activation through mo

About the RoleThis unique hybrid role blends the responsibilities of site startup site navigation and clinical monitoring. As a SCRA / Site Navigator II you will serve as a trusted partner to investigative sites across the full study lifecyclefrom feasibility and activation through mo

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

About the RoleThis unique hybrid role blends the responsibilities of site startup site navigation and clinical monitoring. As a SCRA / Site Navigator II you will serve as a trusted partner to investigative sites across the full study lifecyclefrom feasibility and activation through mo

About the RoleThis unique hybrid role blends the responsibilities of site startup site navigation and clinical monitoring. As a SCRA / Site Navigator II you will serve as a trusted partner to investigative sites across the full study lifecyclefrom feasibility and activation through mo

What if your Pharmacy expertise was the reason a new drug reached patients fasterFortreas Clinical Research Unit in Leeds is a purposebuilt 65000 ft² Phase I facility where lifesaving medicines begin their journey.Here a modern clinic laboratory and cGMP research pharmacy sit under on

What if your Pharmacy expertise was the reason a new drug reached patients fasterFortreas Clinical Research Unit in Leeds is a purposebuilt 65000 ft² Phase I facility where lifesaving medicines begin their journey.Here a modern clinic laboratory and cGMP research pharmacy sit under on

Senior Clinical Data Manager Medical DeviceThe Senior Clinical Data Manager role is a great opportunity to work within our Medical Device Team and have this unique relationship with a sponsor. You will be responsible for the full cycle of Clinical Data Management queries from being i

Senior Clinical Data Manager Medical DeviceThe Senior Clinical Data Manager role is a great opportunity to work within our Medical Device Team and have this unique relationship with a sponsor. You will be responsible for the full cycle of Clinical Data Management queries from being i

*** 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 and LPNs to interact directly with our healthy volunteer participants while learning to read clini

*** 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 and LPNs to interact directly with our healthy volunteer participants while learning to read clini

Job Overview:The Workflow Analyst will hold the responsibilities of performing drug safety and pharmacovigilance support activities as assigned.Summary of Responsibilities:Segregate cases received as per priority and due dates in the database worklist.Assign cases to case processing t

Job Overview:The Workflow Analyst will hold the responsibilities of performing drug safety and pharmacovigilance support activities as assigned.Summary of Responsibilities:Segregate cases received as per priority and due dates in the database worklist.Assign cases to case processing t

Job Overview:Responsible for the analytical support for the developmental projects/comparative dissolution projects and for the proper recording of information.Summary of Responsibilities:Responsible to provide analytical support for the developmental projects/comparative dissolution

Job Overview:Responsible for the analytical support for the developmental projects/comparative dissolution projects and for the proper recording of information.Summary of Responsibilities:Responsible to provide analytical support for the developmental projects/comparative dissolution

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

Fortrea is looking for Senior Biostatistician to join our sponsor dedicated teamAs a Senior Biostatistician at Fortrea you will play a crucial role in the design analysis and interpretation of clinical trials directly impacting the development of innovative therapies and treatments. S

Fortrea is looking for Senior Biostatistician to join our sponsor dedicated teamAs a Senior Biostatistician at Fortrea you will play a crucial role in the design analysis and interpretation of clinical trials directly impacting the development of innovative therapies and treatments. S

Location: Poznań PolandWe are looking for an experienced CRA to join our sponsor-dedicated team in Poznań. This role offers the opportunity to work exclusively with one global sponsor providing strong study continuity deep therapeutic exposure and long-term career development. Key Re

Location: Poznań PolandWe are looking for an experienced CRA to join our sponsor-dedicated team in Poznań. This role offers the opportunity to work exclusively with one global sponsor providing strong study continuity deep therapeutic exposure and long-term career development. Key Re