Clinical Scientist - Level Dependent Upon Experience

CTI; São Paulo; Híbrido; BRL 180 000 - 280 000; Tempo integral

Resumo da oferta

CTI Clinical Trial and Consulting Services in Brazil is seeking a Medical Monitor to oversee clinical trial activities under a medical director. You will review protocols, support sites, and present data to stakeholders, ensuring patient safety and trial integrity.

The role requires strong medical judgment, collaboration with clinical teams, and clear scientific communication. CTI offers a hybrid work model and opportunities to advance in a global CRO environment.

Responsabilidades

• Perform medical monitoring activities under the oversight of a medical director, including protocol and investigator's brochure review, medical budget review, and presenting data to stakeholders.
• Provide guidance to clinical teams on medical and scientific aspects of assigned projects.
• Analyze clinical information and participate in clinical problem-solving and decision-making in trials and studies.
• Lead and participate in medical data and safety reviews, identify safety trends, and follow up with sites/investigators as needed.
• Ensure patient safety and clinical trial integrity.
• Lead department-wide activities to optimize the efficiency and quality of medical services in Medical Affairs.

Descrição da oferta de emprego

About CTI

CTI 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 headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

What You'll Do

• Perform medical monitoring activities under the oversight of a medical director. Medical monitoring activities include but not limited to review of the protocol and investigator’s brochure, review of medical budgets, preparing the medical monitoring plan, training project teams on the protocol, informing site identification and feasibility activities, supporting sites with clinical questions, participating in medical meetings, participating in medical and safety data review and analysis, and preparing and presenting data to internal and external stakeholders.
• Provide guidance to clinical teams on the medical and scientific aspects of assigned projects.
• Analyze and synthesize clinical information, participate in clinical problem-solving and clinical decision-making in the setting of clinical trials and studies.
• Lead and participate in medical data and safety reviews, including identifying critical safety trends and following up with sites/investigators to obtain additional information and to assess clinical events.
• Ensure patient safety and clinical trial integrity.
• Lead project-specific and department-wide organizational activities to optimize the efficiency and quality of medical services in Medical Affairs

What You Bring

• Ability to make clinical decisions under the oversight of an MD, ability to work in collaboration with medical professionals.
• Ability to apply clinical/patient care experience to the research setting in the context of clinical trials.
• Ability to integrate scientific medical data with superior written and oral communication skills.
• Ability to communicate effectively (both verbally and in writing); ability to assimilate complex medical and/or research information; ability to analyze and interpret scientific data.
• Working knowledge of scientific and research principles and techniques of data analysis, interpretation, and clinical relevance
• Working knowledge electronic data capture systems and data visualization tools
• Working knowledge of Code of Federal regulations, ICH Guidelines, Good Clinical Practice, and applicable US regulatory guidance
• Ability to work effectively both independently and in a team setting to develop high quality, scientifically rigorous materials, and presentations.
• Working knowledge of Microsoft Office Suite including Word, PowerPoint, Excel, OneNote, as well as Access, Adobe, SharePoint, and others. Ability to become proficient in new software applications.
• Working knowledge of basic business-related financial and business development concepts
• Strong organizational, problem-solving, and time management skills; flexible and able to pivot to work toward changing priorities and goals; able to multi-task; self-driven and able to work in a fast-paced environment with competing priorities; able to receive constructive criticism and be open to learning new approaches for continued growth
• Advanced clinical degrees (e.g., PharmD, APRN, PA). Candidates with PhD and advanced public health degrees are also eligible.
• Direct experience in clinical research and clinical development, with experience reviewing and interpreting data especially in rare disease, solid organ transplant, hematology/oncology, cell and gene therapy, central nervous system disorders, and other complex indications
• Experience in direct patient care, clinical decision making, and working in collaboration with medical professionals preferred
• Comfortable managing multiple projects and timelines in a fast-paced, deadline-driven CRO setting
• Strong scientific writing and data interpretation skills

Why CTI?

• Advance Your Career – We invest in your professional growth. Our structured mentoring program, leadership development courses, and dedicated training department provide the support you need to excel. We also encourage ongoing education to help you achieve your professional goals.
• Join an Award-Winning Team – Join a global team spanning 60 countries, recognized for its award-winning culture that prioritizes people. We support your work-life balance with hybrid work opportunities. Through our CTI Cares program, you’ll have opportunities to give back to your community and the world.
• Make a Lasting Impact – At CTI, your work directly contributes to advancing medicine. You’ll play a vital role in developing life‑changing treatments for patients with chronic and critical illnesses. Together, we move medicine forward, making a difference for those who need it most.