Empregos atuais relacionados a Study Start Up Associate I - Sao Paulo - ICON plc
-
Study Start-up Associate II
Há 6 dias
São Paulo, São Paulo, Brasil ICON plc Tempo inteiro R$90.000 - R$120.000 por anoFlex Sao PauloICON 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 the future of clinical developmentWe are currently seeking a Study Start Up Associate II to join our diverse and dynamic...
-
Study Start-up Associate II
Há 6 dias
Greater São Paulo Area, Brasil ICON Strategic Solutions Tempo inteiro R$60.000 - R$120.000 por anoFlex Sao PauloICON 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 the future of clinical development.We are currently seeking a Study Start Up Associate II to join our diverse and dynamic...
-
Study Start up Lead
Há 3 horas
São Paulo, São Paulo, Brasil Roche Tempo inteiro R$120.000 - R$240.000 por anoAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...
-
Study Start Up Manager
2 semanas atrás
São Paulo, São Paulo, Brasil Medpace Tempo inteiroOverviewOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo This position plays a key role in the study start up process at Medpace.ResponsibilitiesEfficiently manage and successfully execute all aspects of global...
-
Study Start Up Manager
1 semana atrás
São Paulo, São Paulo, Brasil Medpace Tempo inteiroOverview Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo This position plays a key role in the study start up process at Medpace. Responsibilities Efficiently manage and successfully execute all aspects of global...
-
Study Start Up Manager
Há 6 dias
São Paulo, Brasil Medpace Tempo inteiroOverviewOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo! This position plays a key role in the study start up process at Medpace. ResponsibilitiesEfficiently manage and successfully execute all aspects of global...
-
Study Start Up Manager
Há 7 dias
São Paulo, Brasil Medpace Tempo inteiroOverview Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo! This position plays a key role in the study start up process at Medpace. Responsibilities Efficiently manage and successfully execute all aspects of global...
-
Manager of Study Start Up
Há 2 dias
São Paulo, Brasil ICON Tempo inteiroOverview 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 the future of clinical development. We are currently seeking a Manager, Study Start-Up to join our diverse and dynamic team....
-
Study Start up Specialist I, Biotech
2 semanas atrás
São Paulo, São Paulo, Brasil IQVIA Tempo inteiroStudy Start up Specialist I, IQVIA Biotech Join to apply for the Study Start up Specialist I, IQVIA Biotech role at IQVIA Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and...
-
Study Start Up Manager
2 semanas atrás
São Paulo, São Paulo, Brasil Medpace Tempo inteiroOverviewOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop and...
Study Start Up Associate I
2 semanas atrás
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
**The Role**:
As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.
- Coordinate, balance and facilitate activities related to the completion of Critical Document Package (CDP) and the IP release checklist (SST004-SOP-F01) in accordance with ICH GCP guidelines and all applicable regulations, laws, ethical standards, other guidelines, sponsor requirements
- Ensure that the overall process is focused on quality, efficiency and cost containment for a particular region / sub division within the CDP group, under the general mentorship of Mgr/Sr. Manager - Central Services or Designee.
- To review and negotiate clinical site investigator contracts and budgets.
- Stay connected with Investigative sites, sponsors and internal personnel regarding the status of contracts and contract-related documents
- Prepare and coordinate preparation of contractual documents and correspondence
- Facilitate the indemnification process between the study sponsor and the site.
- Function as the internal consultant on study budgets (investigator payments, develop and update training documentation and conduct group training as necessary, mentor and train new and junior personnel in the SSU department, and act as consultant on the Investigator Contract and Budget development process from origination through execution).
**To be successful in the role, you will have**:
- Bachelor’s Degree preferably in Life Sciences, finance or related experience is preferred.
- Experience or understanding of clinical study start up requirements and activities.
- Experience of Clinical Trial operations and meeting regulatory guidelines
- Experience in contract review and budget negotiation or in related fields such as where contract or legal document review is a primary part of your role
- Proficient project management skills.
**Benefits of Working in ICON**:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
