Empregos atuais relacionados a Clinical Development Analyst - São Paulo, São Paulo - CLINERGY Health Research
-
Clinical Development Analyst
Há 6 dias
São Paulo, São Paulo, Brasil CLINERGY Health Research Tempo inteiroLocation: Brazil (hybrid / remote with on-site visits)Type: 12-month contract (high possibility of further renewals)Clinergy Health is a boutique CRO focused on delivering high-quality, highly tailored clinical development solutions for pharmaceutical and biotech companies operating in Brazil and Latin America.We deliberately work with a selected number...
-
Associate Director Clinical Monitoring
2 semanas atrás
São Paulo, São Paulo, Brasil CTI Clinical Trial and Consulting Services Tempo inteiroAbout CTICTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is...
-
Clinical Lead
Há 6 horas
São Paulo, São Paulo, Brasil IQVIA Tempo inteiroJob OverviewThe Clinical Lead provides leadership of the clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project's overall objectives to the Sponsor's satisfaction per contract while optimizing speed, quality and cost of delivery and in accordance with our SOPs, policies...
-
Clinical Lead
Há 2 dias
São Paulo, São Paulo, Brasil IQVIA Tempo inteiroJob OverviewThe Clinical Lead provides leadership of the clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project's overall objectives to the Sponsor's satisfaction per contract while optimizing speed, quality and cost of delivery and in accordance with our SOPs, policies...
-
Assoc Clinical Lead
2 semanas atrás
São Paulo, São Paulo, Brasil IQVIA Tempo inteiroJob OverviewAssociate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with...
-
Clinical Lead
Há 2 dias
São Paulo, São Paulo, Brasil IQVIA Tempo inteiroThe Clinical Lead provides leadership of the clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project's overall objectives to the Sponsor's satisfaction per contract while optimizing speed, quality and cost of delivery and in accordance with our SOPs, policies and...
-
Clinical Trial Manager II, Biotech
Há 4 dias
São Paulo, São Paulo, Brasil IQVIA Tempo inteiroIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.Job OverviewOncology & Global...
-
Clinical Trial Project Manager, Biotech
2 semanas atrás
São Paulo, São Paulo, Brasil IQVIA Tempo inteiroSao Paulo, Brazil | Full time | Home-based | R1518942IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to...
-
Clinical Trial Project Manager, Biotech
2 semanas atrás
São Paulo, São Paulo, Brasil IQVIA Tempo inteiroIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.Job OverviewOncology & Global...
-
Principal Clinical Research Associate
2 semanas atrás
São Paulo, São Paulo, Brasil CTI Clinical Trial and Consulting Tempo inteiroPrincipal Clinical Research AssociatePlease submit your CV in English for Quickest Review ProcessMaintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or milestone that...
Clinical Development Analyst
3 semanas atrás
Location:
Brazil (hybrid / remote with on-site visits)
Type:
12-month contract (high possibility of further renewals)
Clinergy Health is a boutique CRO focused on delivering high-quality, highly tailored clinical development solutions for pharmaceutical and biotech companies operating in Brazil and Latin America.
We deliberately work with a selected number strategic projects ranging from phase 1 to RWE to ensure scientific rigor, operational excellence, and close collaboration with our clients.
We are now expanding our team and looking for a Clinical Trials Analyst to support our growing portfolio of clinical development projects.
The Role
This position is ideal for a professional with previous experience in clinical trial monitoring who is looking to expand beyond a traditional CRA role looking into further professional development.
As a Clinical Trials Analyst, you will work closely with the Project Lead, supporting key activities across the entire study lifecycle — from start-up through execution — while maintaining hands-on involvement in on-site monitoring.
This is a
hybrid role
, combining:
- Strategic and analytical project-support activities
- Operational involvement in study start-up and trial conduct
- Selective on-site monitoring, with a more balanced travel model
Key Responsibilities
Study Start-Up & Project Support
- Support clinical trial start-up activities (site selection, feasibility support, essential documents, regulatory and ethics submissions follow-up)
- Assist the Project Lead in planning, tracking, and coordinating study activities
- Support the preparation and maintenance of study plans, trackers, and project documentation
- Contribute to risk identification and mitigation activities during study conduct
Trial Conduct & Management
- Support day-to-day trial execution activities, including site communication and issue follow-up
- Assist with oversight of timelines, deliverables, and study milestones
- Participate in cross-functional interactions with sponsors, vendors, and sites
- Contribute to the preparation of reports, status updates, and study documentation
On-Site Monitoring
- Perform on-site monitoring visits according to the monitoring plan (e.g., initiation, routine, and close-out visits)
- Ensure compliance with protocol, GCP, and applicable regulatory requirements
- Review essential documents, source data, and data quality at site level
- Support sites in addressing findings and corrective actions]
Profile We're Looking For
Required
- Background in Life Sciences (e.g., Pharmacy, Biology, Biomedicine, Nursing, or related fields)
- Previous experience in clinical trials monitoring (CRA or similar role)
- Solid understanding of GCP and clinical trial processes
- Willingness to travel for on-site monitoring
- Strong organizational skills and attention to detail
- Good communication skills in English (written and spoken)
Desirable
- Experience supporting study start-up activities
- Exposure to project management or study coordination activities
- Experience working with international sponsors or CROs
Why Join Clinergy Health?
- Broader role than a traditional CRA position
, with exposure to strategic and project-level activities; - Real development opportunity
in clinical trial management and oversight; - Balanced travel model
, avoiding the heavy travel burden typical of monitoring-only roles; - Close collaboration with highly experienced clinical development professionals;
- High scientific and regulatory standards, with real ownership of your work;
- Highly competitive compensation rates.
Note: this role will initially be a 12-month contract position with the possibility of further renewals and/or beaconing a permanente role.
If you are looking to
grow beyond monitoring
, gain a deeper understanding of how clinical trials are planned and managed, and work in a focused, high-quality CRO environment, we would be happy to hear from you.
Applications: online via LinkedIn advertisement or by sending your resume to
