Clinical Services Jobs in Brazil

Job Overview:The Site Activation Coordinator is responsible for supporting and coordinating all activities related to the activation of clinical trial sites from site selection through site initiation. The role ensures that sites are activated efficiently compliantly and on timeline by managing esse...

In a nutshellEurofins endeavors to develop all software applications in-house to service and support our numerous laboratories globally. With hundreds of thousands of clinical diagnostic tests performed every day the laboratories of the Eurofins clinical diagnostic services business line strive to e...

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordinator.This role h...

The DTP Team Lead is responsible for leading a team of Content Design Specialists who ensure translation projects are delivered according to IQVIAs standards and design requirements. He/she builds and maintains strong relationships within his/her team with Project Managers as well as with internal a...

The Operational Effectiveness Specialist 2 is responsible for administering and optimizing proposal development technologies across Commercial Business Optimization & Technology (CBOT) and Research & Development Solutions (R&DS). This role manages user access maintains and updates standard libraries...

The Operational Effectiveness Specialist 2 is responsible for administering and optimizing proposal development technologies across Commercial Business Optimization & Technology (CBOT) and Research & Development Solutions (R&DS). This role manages user access maintains and updates standard libraries...

This is a talent pool for people with disabilities. If you do not belong to this group and wish to apply you can apply for other vacancies within IQVIA jobsImportant: Please submit your CV and laudo when applying.Make an impact on patient healthIQVIAs Global Site Activation Team of 2000 employees dr...

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordinator.This role h...

Key Responsibilities Serve as Regulatory Team Lead on complex global studies including oversight of technical writing and submission publishing. Draft review and quality-check clinical trial regulatory core study documentation at global and country level . Engage directly with clients to clarify cli...

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordinator.This role h...

Job OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budget and resources.Essential Functions Oversee the execution of Site Activa...

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us at IQVIA as - Clinical Trial Educator I Alzheimers (Trilingu...

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordinator.This role h...

PURPOSEThe Content Design Specialist must check content in various languages to ensure it does not contain any design error. He/she must track omission inaccuracy inconsistency and visibility errors coming from OCR translation and DTP tasks. It may entail correcting removing adding and formatting po...

PURPOSEThe Content Design Specialist must check content in various languages to ensure it does not contain any design error. He/she must track omission inaccuracy inconsistency and visibility errors coming from OCR translation and DTP tasks. It may entail correcting removing adding and formatting po...

IQVIA Biotech is hiring for Sr. Site Contracts Associate in Brazil with 3-5 years experience negotiating clinical site contracts and budget templates. Grant Plan a plus.IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therap...

IQVIA Biotech is hiring for Sr. Site Contracts Associate in Brazil with 3-5 years experience negotiating clinical site contracts and budget templates. Grant Plan a plus.IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therap...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and...

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordinator.This role h...

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordinator.This role h...