
Fortrea
Fortrea está com vaga(s) de emprego para Clinical Team Lead – São Paulo em São Paulo
Cargo:
Clinical Team Lead – São Paulo
Requisitos:
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 and technology solutions across more than 20 therapeutic areas. With over 18,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Job Overview:
Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinical aspects of a trial within contractual and budgetary requirements. The CTL oversees the clinical and site management aspects of the trial. The CTL represents clinical delivery with the given customer.
Summary of Responsibilities:
- Take accountability for proactively driving clinical project performance toward contracted deliverables while meeting customer needs and maintaining operational excellence.
- Drive communication and collaboration with the client and project team across a matrixed, multicultural environment.
- Lead the development of the clinical project strategy and ensure prioritization with the clinical project team and key stakeholders in the creation of clear, data-driven strategies and proactive management of project scope, timelines, quality, and budget. In collaboration with relevant departments, prepare and deliver presentations for new business as required.
- Manage the operational aspects of projects to support subject recruitment and retention, clinical vendor delivery, and oversee the monitoring visit strategy.
- Identify clinical project, financial, and quality risks leveraging end-to-end risk management practices and quality by design principles.
- Appropriately utilize data sources, dashboards, and risk management strategies to drive innovation and proactive problem-solving with the project and client teams.
- Adhere to project governance and issue escalation pathways, ensuring that clinical project plans are in place to address identified risk while adhering to professional standards, SOPs, client, and regulatory requirements.
- Partner with project team members and key stakeholders to oversee and manage clinical project budgets, resources, and scope.
- Ensure adherence to established budget and financial milestones. Accountable for accurately forecasting clinical project revenue and managing project costs in adherence to the budget.
- Lead the timely management of changes to scope and the change order process. Ensure project team awareness and tracking of KPIs for any client-specific metrics.
- Provide inspiring leadership and play a key role in the creation of high-performing clinical project teams. Facilitate communication and teamwork while driving delivery, ensuring that clinical team members understand contracted scope, timelines, and budget.
- Ensure that clinical resource projections are accurate and visible to resourcing teams, proactively escalating resource constraints and challenges.
- Develop and mentor team members in multiple areas of expertise and provide feedback as needed to respective line managers.
- As required by the project roles, participate and oversee the regulatory/ethics committee submissions, tracking, and documentation.
- Support new business with active participation in Bid Defense preparation and meetings, as required.
- And all other duties as needed or assigned.
Qualifications (Minimum Required):
- University/college degree (life science preferred) or certification in a related allied health profession (i.e. 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):
- 2+ years clinical research/monitoring experience or an equivalent combination of education and experience to successfully perform key responsibilities of the job.
- Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
- Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access, and PowerPoint).
- Experience managing projects in a matrix and virtual environment.
- Excellent communication, planning, and organizational skills.
- Demonstrated ability to lead by example and to encourage team members to seek solutions independently.
- Demonstrated ability to handle multiple competing priorities and to utilize resources effectively.
- Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system.
- Financial awareness and ability to actively and effectively utilize financial tracking systems.
- Ability to work independently and mentor junior project team members.
- Ability to negotiate and liaise with clients in a professional manner.
- Ability to present to staff at all levels.
Preferred Qualifications Include:
- Master or other advanced degree.
- PMP certification.
- 2+ years CRA experience, on-site or in-house.
- In lieu of the above minimum requirement, candidates with three or more years of relevant clinical research experience in pharmaceutical, CRO, or health care setting will be considered.
Physical Demands/Work Environment:
- Standard Office Environment or remote-based work required.
- Weekend and off-hour work as required.
- Travel Requirements: up to 30% (Global – primary domestic and international).
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If you require a reasonable accommodation to complete your job application, pre-employment testing, job interview, or to otherwise participate in the hiring process, please contact: Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.
Didn’t find what you were looking for? Join our Global Talent Network to stay connected with Fortrea, drive innovation and contribute to our mission of advancing life-saving therapies for patients worldwide.
At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.
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