Clinical Research Manager
TFS HealthScience
TFS HealthScience is a global, mid-sized contract research organization (CRO) partnering with biotechnology and pharmaceutical companies across the full clinical development lifecycle. Our expertise spans full-service clinical development, project-based support, strategic resourcing, and Functional Service Provider (FSP) solutions, matching experienced professionals to roles where they deliver the greatest impact.
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.
Join Our Team as a Clinical Research Manager (CRM) - home based in Argentina or Brazil.
About this role
As part of our Ohtalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. The Clinical Research Manager (CRM) is responsible for coordinating and overseeing country and site management activities throughout study conduct, ensuring high‑quality delivery in accordance with company SOPs, regulatory requirements, and contractual obligations. Key Responsibilities:
Oversee day‑to‑day clinical operations to ensure delivery according to protocol, SOPs, ICH/GCP, and regulatory requirements. Serve as the primary operational contact for Sponsors, providing updates, managing expectations, and ensuring high‑quality study execution. Lead and support CRAs, including training, supervision, performance oversight, co‑monitoring, and review/approval of monitoring visit reports. Ensure site and country performance through proactive review of monitoring activities, protocol deviations, data listings, recruitment progress, and issue escalation. Maintain oversight of study documentation, including TMF quality, CTMS accuracy, monitoring plans, training plans, and study‑specific materials. Collaborate with the Project Manager on study planning, investigator payments, resource allocation, study communications, and revenue forecasting. Contribute to study meetings, Investigator Meetings, feasibility assessments, and, when required, local project management, CRA support, and bid defense activities. Qualifications:
Minimum 5 years of clinical monitoring experience in a CRO, pharmaceutical, or biotechnology environment. At least 1 year of experience as a Clinical Research Manager (CRM) with proven oversight of site and country operations. 1+ years of experience in Ophthalmology (OPH) , ideally within retina indications such as DME, AMD, GA, RVO, or inherited retinal diseases (IRDs). Fluency in English, Spanish and Portuguese is required. Strong understanding of ICH/GCP, regulatory requirements, and clinical operations processes. Demonstrated ability to lead CRAs, manage study deliverables, and collaborate effectively with cross‑functional teams. What We Offer
We provide a competitive compensation package, comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients
A Bit More About Us
Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology and Ophthalmology.
Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration.
Together we make a difference.
Vaga publicada há 10 dias atrás
Empregos semelhantes que podem ser interessantes para vocêCom base na vaga Clinical Research Manager em São Paulo, SP
- ...Oncology Clinical Research Associate (CRA II) Location: Paraíso, São Paulo (Hybrid/Field-Based) Sector: Clinical Research – Biotech Specialist... ...treatments to market. Primary Responsibilities: * Manage the full lifecycle of site visits, including pre-study/selection...
- ...Clinical Research Associate (CRA) São Paulo, Brazil Full Time Job Overvie wWe are seeking... ...will be responsible for monitoring and managing clinical sites to ensure compliance... ...and maintain consistent communication to manage expectations and resolve issues ....
- Clinical Research Associate I, II or Senior (Nordeste) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission...
- ...Paulo ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment... ...processes and regulatory requirements. Proven ability to manage multiple sites and projects simultaneously, with strong organizational...
- ...anticipates and proactively solves study-related clinical site issues as they occur and initiates,... ...standards in conducting clinical research. Conducts site qualification,... ...them to meet study objectives. proactively manages the site and ensures action plans are put...
- ...America , and we’re hiring a Senior Clinical Research Associate to support critical studies... ...Independently oversees all aspects of study site management to ensure patient safety is protected,... ...tools/systems, and status reports Manages site start up procedures including the...
- ...Janeiro or Porto Alegre. Job Summary The Senior Clinical Research Associate I (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned... ...achieve project goals, timelines and quality Manage assigned operational aspects for implementation...
- ...Parexel FSP is actively hiring multiple Clinical Research Associates and Senior Clinical... ...studies. Key Accountabilities : Site Management Responsibilities Contributes to the selection... ...sites as per required timelines. Manages study supplies (Investigator Site File...
- ...compliance of the Monitors in the region. Manages Monitors in the query resolution process... .../process deviation reporting. Performs clinical supplies management with vendors on a... ...Information Advance your career in clinical research, coordinating a variety of tasks and...
- 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, patient access...
- ...limit to what we can achieve. At Parexel, we are a leading Clinical Research Organization (CRO) specializing in delivering life‑changing... ...Collaborate with cross‑functional teams to meet project timelines Manage site‑level study documentation, systems updates, and visit...
- Title Managing Consulting - Senior Research ManagerOverview The Data & Services team is a key differentiator for Mastercard providing the cutting‑edge services that help our customers grow. Focused on thinking big and scaling fast around the globe, this agile team is...
- ...Clinical Trial Manager (FSP - Sponsor Dedicated) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to...Trabalho remoto
- ...office ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment... ...future of clinical development. We are currently seeking a Manager, Clinical Operations to join our diverse and dynamic team. As...
- ...limit to what we can achieve. Parexel FSP is hiring a Manager, Clinical Operations ( Line Manager) to join our growing team in... ...management experience or equivalent experience in clinical research with strong understanding & knowledge of clinical trials environment...
- Clinical Trial Manager (CTM) - Brazil - Homebased ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape...
- ...IQVIA Biotech is seeking a Clinical Project Manager with at least 2 years experience in project management in Cardiovascular, Renal and/or Metabolic... ...field required. Experience: Minimum 5 years in clinical research, including 1+ years in project management. Knowledge:...
- ...including the potential for missing a timeline in the Data Management Project Plan. • Escalate potential quality issues. • Ensure... ...technical designer experience. • 9 years of overall experience in clinical research data management. • Hands-on experience designing in Medidata...
- CLINICAL TRIAL MANAGER - FUTURE ROLES Syneos Health® is a leading fully integrated biopharmaceutical... ...implementation of Phase 1 clinical research studies at the organization's... ...subjects, client teams, investigators, and clinic operations teams, and meticulously plan...
- ...PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the... ...service CRO with a global reach, supporting clinical trials across multiple countries and... ...pharmaceutical industry. Clinical Data Manager plays a critical role in the clinical...
- ...innovative portfolio of technologies to address a patient’s unmet clinical needs. It’s our driving force to help patients live longer and... ...of our inspiring journey. How you'll make an impact: • Manage and oversee the work of clinical field specialist team...
- Job Description Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for.
- ...are focused on helping people with diabetes manage their health through life‑changing products... ...the adoption of Abbott CGM solutions in clinical trials by engaging investigators, supporting country teams, and enabling research sites across more than 30 countries. This is...
- ...: At least 2 years of experience in Clinical Trials (site level, CRO, and pharmacy industry... ...: Supports the Regional Clinical Study Manager in regional study delivery and ensures... ...and budget. Supports the Clinical Research Associates and/or Study Start-up Specialists...
- ...Medicine” We are seeking experienced researchers and scientists to join us as Editorial... ...If you're interested in publishing your Research, click her e. 1 ZD... ...with experience in Medicine Research in clinical, medical, and pharmaceutical research, and...
- Assoc. Cinical Project Manager - Sponsor Dedicated. Clinical Project Management services provide management of a clinical trial (s) in a local level... ...pharmaceutical industry or CRO and previous experience as Clinical Research Associate. • Oncology therapeutic area experience is...
- Job Overview Our FSO team is seeking an Ophthalmology Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires... ...) ~ Minimum of five (5+) years of relevant clinical research experience in a pharmaceutical company/CRO. ~3 years on clinical...
- A EQI Research é a casa de análise de investimentos da EQI, corretora com mais de R$ 50 bilhões sob custódia, apoiando investidores na construção de portfólios diversificados e de longo prazo. Nosso time produz relatórios, recomendações e conteúdos educacionais que auxiliam...
- . Clinical Research Associate São Paulo, SP, Brazil Ready to be the link between groundbreaking... ...the highest standards of trial execution Managing clinical trial sites as the main point... ...management skills, with the ability to manage multiple sites and priorities simultaneously...
- Job Description The Lead Data Manager will be responsible for all data management activities... ...and company departments with regard to clinical data management Communication line for... ...Advance your career in clinical research and develop new skillsets whilst growing...
Deseja receber mais vagas?
Assine e receba vagas semelhantes a Clinical Research Manager. Seja o primeiro a se candidatar!
