Study Start Up Associate Ii

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:...

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 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...

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...

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 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...

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...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in...

**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...

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...

Job Summary">We are seeking a highly motivated Senior Clinical Research Associate II to join our global clinical trial management team. As a key member of the team, you will be responsible for site monitoring and site management for clinical studies according to Fortrea Standard Operating Procedures and Regulatory Guidelines.">About the Role">The Senior...

Overview">LIS Fortrea Development Ltd Sucursal em Portugal is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience.Salary">We offer an estimated annual salary of €65,000 to €80,000, depending on location and experience.Job Description">The Senior Clinical Research...

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...

With unicorn founders like Paul Müller as part of the founders and team, we help outstanding talents and serial entrepreneurs build and scale their ventures. Our three founders - Daniel, Alex, and Florian - are accomplished serial entrepreneurs with a wealth of experience. EWOR's leadership team has built and exited 7 companies before, including a €1.2BN...

With unicorn founders like Paul Müller as part of the founders and team, we help outstanding talents and serial entrepreneurs build and scale their ventures.Our three founders - Daniel, Alex, and Florian - are accomplished serial entrepreneurs with a wealth of experience. EWOR's leadership team has built and exited 7 companies before, including a €1.2BN...

Our client, a leading Global Clinical Research Organization (CRO), is currently seeking a skilled Clinical Research Associate to support their diverse range of Pharmaceutical and Biotech clients in Portugal.Key Responsibilities:Monitor clinical studies in phases II-IIIEnsure adherence to Good Clinical Practices and investigator integrityIdentify, qualify,...

Unlock your potential as a Senior Clinical Study Manager at Mygwork - LGBTQ+ Business Community, where diversity and inclusion thrive. We are seeking an experienced professional to lead clinical trials with moderate complexity, providing quality oversight and driving decision-making.Job SummaryAs a Senior Clinical Study Manager, you will be responsible for...

About UsWe're an innovative start-up that prioritizes cutting-edge technology in all our projects. We're seeking a skilled CTO - Chief Technology Officer (Full Remote) to lead our tech strategy and drive growth from the comfort of their home.Your Responsibilities:Develop and implement a comprehensive tech vision, positioning us as a key player in the...

At Iqvia, we are seeking a highly skilled Clinical Study Support Specialist to join our team. This role is an excellent opportunity for individuals who are passionate about the pharmaceutical industry and want to make a difference in patient care.As a Clinical Study Support Specialist, you will be the primary point of contact for patients and healthcare...

**Research Study Nurse***: **Localização**: Centro Champalimaud **Entidade Empregadora**: Fundação Champalimaud **Regime**: Tempo Inteiro **Posição**: Enfermagem **Início da Candidatura**: 02 Dez. 2024 Offer Description Main duties will include - Coordinate translational research studies, including participant recruitment, enrollment, and...