Clinical Research Medical Advisor

The Role of a Clinical Research Medical AdvisorThis is an exciting opportunity to work with our team, leading clinical research and development initiatives that make a meaningful impact in the lives of patients.About the JobWe are seeking an experienced Clinical Research Medical Advisor to join our team. As a key member of our organization, you will be...

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...

**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...

**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...

**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...

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...

**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...

**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**:- Agile cross-functional collaboration to ensure we are prepared for strategic and frequently asked questions. -Continuously improving our reactive positionings according to their monitored effectiveness -Implementation of a lean but impactful process when dealing with non-prioritize portfolio**About the Role**:**Work Model**:Hybrid**Locality**:...

Job Title: Pharmaceutical RepresentativeDrive competitive sales growth by identifying and prioritizing high-potential customers through data analysis who influence prescription decisions.Build relationships with healthcare professionals to understand their challenges, decision-drivers, pain points, and opportunities.Personalize customer engagement journeys...