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Manager Fortrea Jobs (NOW HIRING)

Fortrea is seeking Clinical Trial Managers to join our team! We are seeking experienced CTLs with 3+ years of experience. . Remote US or Canadian based. We are seeking candidates with either CAR T or ...

Job Overview: Corporate Counsel provides legal support and counseling for Fortrea and their ... Knowledge management, including preparation and organization of work product, administration of ...

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Bachelor's degree - Life Sciences and/or Business Management. * Fluent in English, both written and verbal. * Fortrea may consider relevant and equivalent experience in lieu of educational ...

... management system aligned with global regulatory expectations and Fortrea business strategy. Leads the design, implementation, and continuous improvement of audit, inspection readiness, and quality ...

... growth within Fortrea. In addition, they are expected to establish and develop strong client ... Participates in risk management activities across the assigned portfolio of studies to support the ...

Bachelor's degree - Life Sciences and/or Business Management. * Fluent in English, both written and verbal. * Fortrea may consider relevant and equivalent experience in lieu of educational ...

Fortrea is seeking Oncology Clinical Team Leads to join our FSP team! We are seeking experienced ... CTLs partner with the Project Manager and other functional leads to ensure successful delivery of ...

Project Managers own the operational strategy, determining the most cost effective and efficient ... Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Project Managers own the operational strategy, determining the most cost effective and efficient ... Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Senior Biostatistician - FSP

Durham, NC · On-site

$115K - $135K/yr

Perform project management activities for identified projects including resource planning ... Fortrea may consider relevant and equivalent experience in lieu of educational requirements. * Must ...

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Manager Fortrea information

What is the difference between Manager Fortrea vs Clinical Project Manager?

AspectManager FortreaClinical Project Manager
CredentialsBachelor's degree, relevant certifications (e.g., PMP)Bachelor's degree, often PMP or similar certifications
Work EnvironmentPharmaceutical/biotech industry, office and site visitsClinical research settings, hospitals, offices
Employer & IndustryFortrea (biotech/pharma)Pharmaceutical companies, CROs
Search & Comparison IntentYesYes

The Manager Fortrea typically oversees multiple projects within the biotech or pharmaceutical industry, focusing on strategic management and team leadership. A Clinical Project Manager primarily manages individual clinical trials, ensuring compliance and timely delivery. While both roles require similar credentials and work in related environments, the Manager Fortrea has a broader scope, often involving higher-level planning and coordination across projects.

What cities are hiring for Manager Fortrea jobs? Cities with the most Manager Fortrea job openings:
What are the most commonly searched types of Fortrea jobs? The most popular types of Fortrea jobs are:
What states have the most Manager Fortrea jobs? States with the most job openings for Manager Fortrea jobs include:
Clinical Trial Manager - CAR T or Ophthalmology

Clinical Trial Manager - CAR T or Ophthalmology

Fortrea

On-site, Remote

Full-time

Re-posted 11 days ago


Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

19th of 60 rated research


Job description

Fortrea is seeking Clinical Trial Managers to join our team! We are seeking experienced CTLs with 3+ years of experience. . Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology experience.
Job Overview:
The Clinical Trial Manager has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract, ensuring quality, compliance and meeting country-specific commitments.
The role generally works under the direction of a (Senior) Clinical Trial Manager, however, may also work independently at a lower complexity study.
Summary of Responsibilities:
  • End-to-end oversight of start-up and clinical responsibilities-from site identification through to database lock-through proactive management of project scope, timelines, milestones, and budget.
  • Ensure start-up and clinical project plans address identified risks while adhering to professional standards, SOPs, client, and regulatory requirements.
  • Proactively identify and address start-up and clinical project, financial, and quality risks by applying comprehensive risk management strategies and ensuring compliance, including tracking within applicable systems.
  • Responsible for financial aspects of clinical and start-up activities, including revenue forecasting, adherence to contracted scope, and oversight of scope modifications.
  • Ensure project team awareness and tracking of Key Project Indicators (KPI) for any client-specific start-up and clinical metrics.
  • Ensure and plans for start-up and clinical resources with accurate projections for the resourcing teams.
  • Develop and implement the site activation and recruitment strategy in collaboration with project teams.
  • Lead and oversee site identification and site selection.
  • Oversight of Informed Consent Form development and translations.
  • Oversight of essential document creation and collection, including insurance.
  • Oversight of the development, negotiation, and execution of Clinical Trial Agreements (CTA), including site budgets.
  • Lead the end-to-end process of regulatory/ethics committee submissions, approvals, and tracking.
  • Ensure clinical and ancillary supplies -including import/export logistics and supply destruction processes- are in place as applicable.
  • Manage operational aspects to support subject recruitment and retention, patient safety, vendor performance, and the monitoring visit strategy.
  • Proactive planning for monitoring activities to ensure data integrity, patient safety and endpoint protection.
  • Ensure inspection-readiness through quality oversight of TMF, monitoring reports, protocol deviations and issue management.
  • Oversight and approval of site payments, including payment reconciliation.
  • Foster effective communication and collaboration with clients and cross-functional project teams in a global and multicultural environment.
  • Ability to lead client-facing calls to communicate project status updates and demonstrate operational control of start-up and clinical deliverables.
  • Support new business with active participation in pre-award preparation as required.
  • Provide feedback on team members as needed to respective line managers.
  • All other duties as needed or assigned.

Qualifications (Minimum Required):
  • University/college degree (life science preferred) or certification in a related allied health profession (nursing, medical, or laboratory technology) from an appropriately accredited institution.
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
  • Fluent in English, both written and verbal

Experience (Minimum Required):
  • Four or more years of relevant clinical research experience in pharmaceutical, CRO, or health care setting will be considered.
  • Previous SSU and Clinical Trial Lead experience
  • CAR T or Ophthalmology experience
  • Comprehensive knowledge of GCP, ICH, and regulatory guidelines.
  • Proficiency in Microsoft Office and familiarity with EDC, CTMS, eTMF, and vendor platforms (e.g. Veeva Vault, Medidata).
  • Effective leadership in remote and global environment.
  • Strong communication, planning, and organizational abilities.
  • Proven team motivational skills.
  • Proficiency in balancing concurrent tasks within time-sensitive environments.
  • Financial awareness and use of tracking systems/tools.
  • Demonstrated independent problem-solving and risk management mindset.
  • Demonstrated professional client interaction and presentation skills, with ability to work independently and collaboratively.

In this role, employees will leverage their existing experience and skills to assume additional responsibilities within the broader role. These will be aligned with operational requirements and internal training, without altering the fundamental nature or classification of the position.
Preferred Qualifications Include:
  • Master's or other advanced degree.
  • PMP certification or equivalent.

Physical Demands / Work Environment:
  • Remote-based work required with possible office presence depending on location.
  • Travel requirements: up to 20% (global - primarily domestic and international)

Pay Range: $140,000-148,000 USD annually
Learn more about our EEO & Accommodations request here.

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