Clinical Research Specialist

**Summary**:The professional will be responsible for Contributes, with appropriate oversight, to all relevant aspects of global clinical trial(s) activities to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial Team. -Applicable...

About the RoleKey ResponsibilitiesValidate study designs and assess trial feasibility based on clinical practice and competitive analysis.Drive fast and high-quality trial site start-up through expert input during planning phases.Provide clinical expertise for IRB/EC interactions and informed consent content.Develop trial plans that address recruitment...

About the Role Key Responsibilities Validate study designs and assess trial feasibility based on clinical practice and competitive analysis. Drive fast and high-quality trial site start-up through expert input during planning phases. Provide clinical expertise for IRB/EC interactions and informed consent content. Develop trial plans that address recruitment...

**Summary**:Site relationship management role to ensure sustainable trial execution at Site. Performs on-site and remote monitoring activities related to initiation, conduct and timely completion of Phase I-IV GDD trials within the country in adherence with monitoring procedures and processes in accordance with ICH/GCP, local regulations and SOPs. Proactive...

**Summary**:Site relationship management role to ensure sustainable trial start-up at Site.The Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I-IV GDD trials within the country in adherence with monitoring procedures and processes in accordance with ICH/GCP,...

**Summary**:Lead scientific engagement with their Medical Experts.Implement clinical and educational strategies and respond to unsolicited medical enquirers.**About the Role**:Work Model: on-siteLocation: Rio de Janeiro (RJ)Travel Sector: Rio de Janeiro and Parana states**Major accountabilities**:- Engage with Medical Experts to educate on medical/scientific...

Expert Clinical AdvisorJob OverviewWe are seeking a skilled expert to provide clinical guidance on study designs and trial feasibility.The ideal candidate will drive fast and high-quality trial site start-up through expert input during planning phases.Responsibilities include providing clinical expertise for IRB/EC interactions and informed consent...

Job Title:Access and Healthcare Lead">Job Description:">As a key member of our team, you will be responsible for developing and implementing innovative access strategies for our brands.You will work closely with cross-functional teams to co-create the brand strategy and lead an innovative access strategy for brands in collaboration with PAGs, Medical,...

**Summary**:Na Novartis, nosso compromisso é reimaginar a medicina. Como Associado de Ensaios Clínicos (CTA), você será peça-chave no suporte ao Gerente de Início de Estudos da SSO e ao Gerente de Projetos Clínicos da SSO nos estudos designados. Você contribuirá durante a configuração e todo o ciclo de vida do estudo, garantindo conformidade com...

**Summary**:Lead the development and execution of country Medical Affairs Plan. Be an accountable scientific partner communicating externally and internally. Keep up to date with key developments in own TA. Gather and share insights with global, region and country local stakeholders**About the Role**:**Key responsibilities**:- Develop and implement country...