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Manager Fortrea Jobs (NOW HIRING)

Fortrea

$90K - $110K/yr

Clinical Study ICF Writer - US Remote based Fortrea is looking for a confident, seasoned Doc Review ... Liaising and follow-up with local teams, Start-up Project Managers, and Sponsors to assure timely ...

Fortrea

Clinical Team Lead, FSP - Oncology

Durham, NC · Remote

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 ...

New

Fortrea

QA Lead Sr. Manager

Durham, NC · On-site

Manages the QA-to-QA relationship with assigned key client(s). * Participates in client JOC or ... Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Fortrea

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

Fortrea

Clinical Team Lead, FSP - Oncology

Durham, NC · Remote

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 ...

New

Fortrea

Biostatistician I

San Jose, CA · On-site +1

Fortrea may consider relevant and equivalent experience in lieu of educational requirements ... Office or home-based environment, as requested by the line manager. * Travel Requirements: * % of ...

Fortrea

Senior Statistical Programmer

San Jose, CA · Remote

Fortrea may consider relevant and equivalent experience in lieu of educational requirements ... Office or home-based environment, as requested by the line manager. * Travel Requirements: Yes.

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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.

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What are the most commonly searched types of Fortrea jobs? The most popular types of Fortrea jobs are:
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Manager Fortrea jobs near you

Monitoring Excellence Academy - OMEA - Oncology / CAR T & Ophthalmology - CRA 1

Fortrea

Manhattan, NY • Remote

$80/hr

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Fortrea rating

7.2

Company rating: 7.2 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

44th of 56 rated research

Job description

Fortrea's Monitoring Excellence Academy is hiring!! We are seeking strong, Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses with 2+ years of current experience. Must have 2+ years of Oncology, CAR T or Ophthalmology as a CRC or research nurse. Open to various hub locations around the US and French Speaking candidates in Montreal, Canada. Must be willing to travel 65-70%.
WHAT YOU WILL DO
You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.
Responsibilities:
  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
  • Responsible for all aspects of site management as prescribed in the project plans
  • General On-Site Monitoring
  • Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
  • Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  • Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
  • Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
  • Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
  • Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
  • Assist with training of new employees, eg. co-monitoring
  • Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
  • Perform other duties as assigned by management
Requirements
  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
  • 2+ years as a Study Coordinator or Research Nurse in specified therapeutic areas
  • Oncology experience is strongly desired ; CAR T a plus
  • 60-70% overnight travel
The important thing for us is you are comfortable working in an environment that is:
  • Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
  • Changing priorities constantly asking you to prioritize and adapt on the spot.
  • Teamwork and people skills are essential for the study to run smoothly.
  • Technology based. We collect our data directly into an electronic environment.
Work Environment:
  • Work is performed in an office environment with exposure to electrical office equipment.
  • Frequent travel to clients/ site locations with occasional travel both domestic and international.
Physical Requirements:
  • Ability to sit for extended periods and operate a vehicle safely.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Regular and consistent attendance.
  • Varied hours may be required.
  • Target Pay Range: $80-90K

#LI - Remote
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