Fortrea Salary

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  Leeds
Rating of the company
based on 0 evaluations
2 reviews in total

Earnings on positions in Fortrea

Estimated salary

£ 1999

Median salary at Fortrea

£ 1760 Lowest salary
£ 6231 The average salary
£ 19166 Highest salary

Fortrea is looking for employees for positions:

project manager

Working hours

  • full-time

Language

  • english

Responsibility

  • we are looking for a Study Start-Up Project Manager to be 100% home based anywhere in the UK
  • this particular job will be 100% client dedicated with a global Pharmaceutical company
  • the main responsibilities will be regulatory tasks and also budget/finance tasks
  • this position has a significant impact on how the UK can deliver country-specific trial commitments and objectives, especially during start-up
  • as a leading global contract research organization 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 solutions across more than 20 therapeutic areas
  • qualifications, Skills and Experience
  • with over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe
  • this role would suit either an experienced CRA, perhaps looking for less travel, or an existing Study Start-up specialist looking for a more senior & progressive role

clinical services manager

Working hours

  • full-time

Responsibility

  • prepare robust business planning through accurate budgeting/forecasting
  • assist the preparation of financial plans to understand the drivers of revenues and costs
  • conduct monthly variance analyses
  • identify & lead process improvement
  • as a leading global contract research organization 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 solutions across more than 20 therapeutic areas
  • dynamic business partner who leverages relationships to drive financial planning
  • with over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe
  • work with Controllership/Finance Shared Services to review and ensure the accuracy of financial reports

Education

  • bachelor Degree in Finance or Related Field required
  • strong candidates with a lot of FP&A experience would also be considered

Requirements

  • strong networking, team working and relationship management skills
  • strong experience in FP&A or corporate finance
  • strong business acumen; understands business implications of decisions
  • strong problem solving skills and sound judgement
  • supports and explains reasoning for decisions/recommendations
  • excellent written and verbal communication skills
  • proven ability to work independently
  • experience in a matrixed, multi-site, multinational environment strongly preferred

procurement manager

Working hours

  • full-time

Responsibility

  • fortrea is seeking an Experienced Sourcing and Procurement Sr
  • monitor supplier performance, conduct regular audits, and address any quality or delivery issues in a timely manner
  • stay updated on industry trends, regulatory changes, and best practices in procurement to drive continuous improvement in the sourcing process
  • manage procurement budgets, track expenses, and report on cost-saving initiatives to senior management
  • manager to develop relationships and manage stakeholders across the region to identify strategic business needs and to develop and implement sourcing and procurement strategies that align with the organization’s business objectives and compliance standards
  • lead cross-functional teams in the development of RFPs, RFIs, and RFQs to support procurement activities
  • as a leading global contract research organization 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 solutions across more than 20 therapeutic areas
  • implement efficient inventory management practices to prevent shortages and minimize excess stock

Requirements

  • minimum of 5 years of experience in sourcing and procurement, preferably within the pharmaceutical, biotechnology, or CRO industry
  • proven track record of successfully managing end-to-end procurement processes, including supplier selection, negotiation, and contract management
  • strong understanding of regulatory requirements impacting procurement in the clinical research field
  • excellent communication, negotiation, and interpersonal skills to effectively collaborate with internal teams and external suppliers
  • demonstrated ability to analyze data, make informed decisions, and implement process improvements
  • proficiency in procurement software and tools; experience with ERP systems is desirable
  • ability to work independently, manage multiple priorities, and thrive in a fast-paced environment
  • working knowledge of data analysis and forecasting tools and ability to develop actionable insights from data

lead developer

Working hours

  • full-time

Responsibility

  • join a small team of Developers in Fortrea’s Market Access Consulting group delivering digital solutions to pharmaceutical and medical technology clients
  • as a leading global contract research organization 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 solutions across more than 20 therapeutic areas
  • desktop, tablet or online) and purpose (e.g
  • with over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe
  • data display, presentation or eLearning)
  • you will develop a range of interactive web-based solutions for online and offline use that help our clients communicate Health Economics and Outcomes Research and Value Demonstration messaging to various audiences
  • you will have input on projects at every stage of their lifecycle – from concept through to completion – and contribute to the further growth and development of this exciting area of our business
  • they provide mentoring and development of team members whilst ensuring projects are completed on time and on within budget

Requirements

  • degree level qualification in a relevant area and at least five years of relevant, professional experience
  • excellent knowledge of HTML, CSS, JavaScript, JQuery and associated libraries
  • good understanding of development methodologies and practices, including version control
  • good understanding of the concepts of programming, including web-based and other application development, relevant design methods and best practice
  • knowledge of emerging technologies and platforms
  • develop design ideas appropriate for final delivery
  • high level of motivation to improve work processes and identify optimal solutions
  • write clean, stable, usable and tested code and accompanying documentation where needed

developer

Working hours

  • full-time

Responsibility

  • SAS Developer/Analyst
  • in this role you will design and execute processes related to programming, setup, support of clinical and/or safety databases in SAS
  • as a SAS Programmer you are central to the successful delivery of complex clinical trials for renowned, innovative and global top pharmaceutical companies
  • rewarding and meaningful work in an established, diverse, highly profitable and respected global company
  • this position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas such as oncology, cardiovascular, respiratory, neurological, diabetes, rare diseases, pain, immunology etc
  • highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc
  • your expertise and your work as a Biostatistician has a direct impact on improving the health and lives of thousands of patients around the globe every day
  • A genuine work life balance

office manager

Working hours

  • full-time

Language

  • english

Responsibility

  • participate in proposal development for standalone, small programs and/or new drug applications and in bid defenses
  • actively monitor staff projects quality, timelines and budgets to foresee and correct issues and assure project expectations are met
  • manage discretionary expenses and spending within your team in order to meet budget
  • work closely with lead programmers to ensure that staff resources are used efficiently, and team is well utilized
  • as a leading global contract research organization 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 solutions across more than 20 therapeutic areas
  • with over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe
  • as a Manager Statistical SAS Programming in our sponsor-dedicated Flexible Solutions business unit, you and your team are central to the successful delivery of complex clinical trials for renowned, innovative and global top pharmaceutical companies
  • rewarding and meaningful work in an established, diverse, highly profitable and respected global company

Requirements

  • degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc
  • profound professional experience managing a team of statistical programmers working on complex clinical trials within a biotech, CRO or pharmaceutical company
  • solid experience with complex oncology clinical trials and the corresponding datasets and endpoint
  • expert knowledge of base SAS, SAS macros, SAS/STAT and in debugging SAS programs
  • expert knowledge of all CDISC requirements including Reviewer's Guides and submission standards
  • excellent organizational, time management and project management skills with demonstrated leadership experience and a strong business acumen
  • in lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in statistical programming
  • deep knowledge in all aspects of clinical trials, from initial study set-up to study completion, with an excellent understanding of the roles and responsibilities of all related disciplines, e.g. Biostatistics and Clinical Data Management

office junior

Working hours

  • full-time

Language

  • english

Responsibility

  • develop and maintain programs using SAS to create CDSIC SDTM and ADaM datasets as well as Tables, Figures and Listings
  • following department guidelines perform self-checks of code and outputs to ensure first time quality
  • effective time management in order to meet delivery deadlines
  • communicate accurate and timely status updates to line manager, lead programmer, and other associates
  • as a leading global contract research organization 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 solutions across more than 20 therapeutic areas
  • with over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe
  • our dedicated Statistical Programmers in our Clinical Development Services and Clinical Pharmaceutical Services business units are central to the successful delivery of complex clinical trials for renowned, innovative and global top pharmaceutical and biotech companies
  • rewarding and meaningful work in an established, diverse, highly profitable and respected global company

Requirements

  • degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc
  • ideally, an interest in life sciences, particularly medicine, biology and drug development
  • strong organizational and communication skills
  • ability to learn new systems and flourish in an evolving technical environment
  • A collaborative work style, good problem solving abilities. and a keen attention to detail
  • fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials
  • in lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in programming
  • for more information about Fortrea, visit www.fortrea.com

manager

Language

  • english

Requirements

  • university / college degree
  • university / college degree in life sciences, health sciences, information technology or related subjects preferred
  • fortrea may consider relevant and equivalent experience in lieu of educational requirements
  • knowledge of science or a scientific background is preferred
  • experience and/or education plus relevant work experience, equating to a bachelor's degree will be accepted in lieu of a bachelor’s degree
  • thorough knowledge of Fortrea, the overall structure of the organization and Standard Operating Procedures
  • additional relevant work experience will be considered in lieu of formal qualifications
  • 6 to 8 years of DM experience with minimum of 1 years of direct sponsor management

Responsibility

  • lead studies including a combination of healthy volunteer and patient populations, multi-site, client management required or reduced timelines. Ability to organize and effectively prioritize workload and deliverables
  • performs other related duties as assigned by Line Management
  • be accountable for all DM deliverables as assigned per the established timeline; providing instruction to their DM study team and review of their study team’s output to ensure the highest quality, while adjusting resource allocations accordingly
  • ensure that all allocated projects are carried out in strict accordance with the relevant protocols, global harmonized SOPs, and the specified standards of GCPs
  • develop and maintain client relationships and review client satisfaction surveys
  • track scope changes and work with the Project Manager to ensure that Sponsor approval is received, and the scope change processed
  • work with the Project Manager to build timelines to meet contracted milestones by communicating with leads in different disciplines and the full project team as necessary, including at study initiation meetings
  • provide DM project team leadership and accountability; leads data focused internal project team meetings; meets frequently with the study leads of EDC Design, SAS Programming, Statistics, and PK to ensure that all deliverables are planned and coordinated intradepartmental; proactively identifies potential risks/mitigations, effectively communicates data-driven discussions in order to achieve database lock dates; keeps the Project Manager apprised of project progress

nurse

Trade

  • nursing
  • Nursing

Working hours

  • full-time

Responsibility

  • ensure that the dignity, health, safety and welfare of participants is given the highest priority at all times
  • as of March 2023, we moved our Leeds Clinical Research Unit to a state-of-the-art site at Drapers Yard, Leeds
  • perform study related activities such as cannulation, telemetry, holters, vital signs, ECGs, venipuncture
  • based a short walk from Leeds station
  • take responsibility for quality control of study data
  • administer investigational compounds to participants according to the protocol and applicable regulations
  • are you a band 5 or recently registered Nurse and considering a career outside of the NHS?
  • respond to emergency situations based upon nursing standards

Requirements

  • recent nursing experience would be beneficial but is not essential
  • changing priorities constantly asking you to prioritize and adapt on the spot
  • we offer a competitive salary and benefits package
  • teamwork and people skills are essential for the study to run smoothly
  • technology based. We collect our data directly into an electronic environment

administrator

Trade

  • physicians & Surgeons
  • scientific Research & Development
  • Physicians & Surgeons
  • Scientific Research & Development

Responsibility

  • liaise with GPs and surgeries to expedite return of GP Reports and collate GP Reports for review
  • record receipt of GP reports into databases, preparing the updates needed
  • scan, quality check and file GP Reports as appropriate
  • liaise between physicians and GPs to clarify queries
  • notify the GPs of their patient's inclusion in studies
  • enter medical history and demographic information from potential subjects into computerized database
  • receive GP Report Consent Forms from potential subjects and amend the Recruitment Participants database accordingly. Review GP Report Consent Forms for completeness, prior to sending to relevant GP
  • communicate study information to potential subjects

Requirements

  • you must live in commuting distance of Central London, again essential
  • basic understanding of biology and biological processes
  • good organizational and time management skills
  • a minimum of 12 months of Clinical Research Admin experience from a CRO or Pharma company - This is essential
  • a minimum of 12 months of Clinical Research Admin experience from a CRO or Pharma company- This is essential