Study Start Up Associate Ii

6 meses atrás


Lisboa, Portugal ICON plc Tempo inteiro

Study Start Up Associate II

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.

Study Start Up Associate II

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.

The Role
- 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).

What you need
- A bachelor’s degree in Paralegal Studies, Juris Doctor (law) degree, or related experience is preferred
- SSU experience is desirable but not required.
- Experience in a clinical research environment with specific experience in study contracts review and budget negotiation or in related field such as where contract or legal document review is a primary part of you role.

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.



  • Lisboa, Portugal ICON Tempo inteiro

    Study Start Up Associate II 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:...


  • Lisboa, Portugal ICON Plc Tempo inteiro

    Study Start Up Associate II - Fluent Dutch Required 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 Study Start Up Associate / Regulatory...

  • Study Start Up Associate

    5 meses atrás


    Lisboa, Portugal ICON plc Tempo inteiro

    Study Start Up Associate 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:...

  • Study Start Up Associate

    5 meses atrás


    Lisboa, Portugal ICON plc Tempo inteiro

    Study Start Up Associate - Spanish & Portuguese Speaker - Home Based 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...


  • Lisboa, Portugal Icon Plc Tempo inteiro

    Study Start Up Associate II - Fluent Dutch RequiredICON 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.What You Will Be Doing:Leading the preparation and...

  • Study Start Up Specialist

    5 meses atrás


    Lisboa, Portugal TFS HealthScience Tempo inteiro

    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** **Study Start Up Specialist - (home...


  • Lisboa, Lisboa, Portugal Icon Plc Tempo inteiro

    Embark on a challenging career opportunity as a Regulatory Affairs Specialist at Icon Plc, a leading healthcare intelligence and clinical research organization.We are seeking an experienced individual to lead the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency...

  • Clinical Study Associate

    2 semanas atrás


    Lisboa, Lisboa, Portugal Syneos Health Tempo inteiro

    Clinical Study AssociateSyneos Health is seeking a highly skilled Clinical Study Associate to join our team. As a Clinical Study Associate, you will be responsible for performing site qualification, site initiation, interim monitoring, site management activities and close-out visits. You will ensure regulatory, ICH-GCP and/or Good Pharmacoepidemiology...


  • Lisboa, Portugal Iqvia Argentina Tempo inteiro

    Clinical Trial Administrator, Single Sponsor dedicatedJob Overview:CTA performs daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. By assisting in the coordination and administration of the study activities from the start up to...


  • Lisboa, Portugal Iqvia Argentina Tempo inteiro

    Clinical Trial Administrator, Single Sponsor dedicated Job Overview:CTA performs daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. By assisting in the coordination and administration of the study activities from the start up to...


  • Lisboa, Lisboa, Portugal Icon Strategic Solutions Tempo inteiro

    Job Title: Clinical Research Associate IIAt ICON, we are seeking a highly motivated and experienced Clinical Research Associate II to join our team. As a Clinical Research Associate II, you will be responsible for monitoring multiple Phase I, II, III, and IV clinical trial sites, across different therapeutic areas.Key Responsibilities:Monitor multiple...


  • Lisboa, Portugal Iqvia Argentina Tempo inteiro

    Clinical Trial Administrator, Single Sponsor dedicated Job Overview: CTA performs daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. By assisting in the coordination and administration of the study activities from the start up...


  • Lisboa, Portugal Iqvia Tempo inteiro

    Clinical Trial Administrator, Single Sponsor dedicatedJob Overview:CTA performs daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. By assisting in the coordination and administration of the study activities from the start up to...


  • Lisboa, Portugal Allucent Tempo inteiro

    **CATO SMS and Pharm-Olam, LLC have merged to form Allucent!** **Allucent **is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical...


  • Lisboa, Lisboa, Portugal Icon Tempo inteiro

    Job Summary:We are seeking a highly skilled SITE ACTIVATION LEAD to join our team at ICON. As a key member of our clinical operations team, you will be responsible for advancing clinical trial start-up activities and ensuring the successful delivery of our projects.Key Responsibilities:• Advance clinical trial start-up activities by understanding client...

  • Clinical Research Associate

    2 semanas atrás


    Lisboa, Lisboa, Portugal Resourcing Life Science Tempo inteiro

    **About the Role**At Resourcing Life Science, we're seeking a skilled Clinical Research Associate to join our team in Portugal. As a key member of our team, you'll be responsible for monitoring clinical studies in phases II-III, ensuring adherence to Good Clinical Practices and all applicable laws.**Key Responsibilities**Identify and qualify investigators...


  • Lisboa, Portugal Engineeringuk Tempo inteiro

    As a Clinical Research Associate, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas. Assist other CRAs with co-monitoring activities both remote and...


  • Lisboa, Portugal Icon Strategic Solutions Tempo inteiro

    As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas. Assist other CRAs with co-monitoring activities both remote and...

  • Recruiting Associate

    5 meses atrás


    Lisboa, Portugal proSapient Tempo inteiro

    Every day, somewhere in the world, important decisions are made. Whether it is a private equity company deciding to invest millions into a business or a large corporation implementing a new strategic direction, these decisions impact employees, customers, and other stakeholders. Consulting and private equity firms come to proSapient when they need to...


  • Lisboa, Lisboa, Portugal Thermo Fisher Scientific Tempo inteiro

    About UsAt Thermo Fisher Scientific, we are dedicated to enabling our customers to make a positive impact on a global scale. With a mission to accelerate research and solve complex scientific challenges, we strive to drive technological innovation and support patients in need.Our OpportunitiesWe are seeking a highly skilled Clinical Research Associate to...