Clinical Trial Coordinator - Inscuinatoyac

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs , spanning 2 ,700 clinical trials across · 100+ countries in the last 5 years. · Join Us as a Clinical Research Associate I – Make an Impact at the Forefront of Innovation , As part of ...

Job Summary · We are seeking an experienced Clinical Research Associate to join our team. The successful candidate will have a strong background in clinical trials and excellent communication skills. · ...

This is a home-based position that manages country submissions and provides regulatory strategy advice. The role involves preparing, reviewing and coordinating local regulatory submissions, providing technical expertise and coordination oversight for projects in collaboration wit ...

Join us as a project manager. At Thermo Fisher Scientific you will discover meaningful work that makes a positive impact on a global scale. · ...

Join us in bringing our Mission to life - helping customers create a healthier, cleaner and safer world. · ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, · We join Us as a Safety Writer III– Make an Impact at the Forefront of Innovation · As part of our expert team,you'll have the opportunity to ensure operational excellence that makes a ...

Join us as a Senior Clinical Research Associate (Level I) to perform and coordinate all aspects of the clinical monitoring and site management process. · ...

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We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs in the last 5 years. · As a Drug Safety Specialist, you'll perform day-to-day Pharmacovigilance (PV) activities within a highly regulated environment driven by strict timelines. · ...

Join us as a Clinical Systems Testing Specialist and make an impact at the forefront of innovation. · Serve as testing lead and/or support for new releases and modifications to applications throughout the software development process. · ...

We are seeking a Safety Admin to join our global team and provide contracted project coordination and safety support on global and domestic programs. · Coordinates the timely review of protocol inquiries, serious and non-serious adverse events, diagnostics and Data Safety Monitor ...

Join us as Project Manager Clinical Supplies - To manage the end-to-end supply chain for clinical trials, ensure timely and efficient distribution of trial materials, maintain optimal inventory levels, · Bachelor's degree or equivalent · Previous experience that provides knowledg ...

Join Us as a Clinical Data Associate I – Make an impact at the forefront of innovation. · ...

The Sr. CDM Programmer works with and has hands on experience of clinical data management systems like Medidata Rave & Veeva Vault. Provides technical leadership in data management activities and deliverables including database development and data validation. · ...

This is an entry-level role within the Commercial organization supporting Account Development Representatives across all Clinical Research Group service offerings. · ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, · As part of our global team, you'll have the opportunity to prepare and negotiate contracts, · As a Site Contract Specialist, you'll liaise and establish effective relationships with s ...

This role entails providing visible scientific leadership, collaborating with key opinion leaders, and delivering successful clinical trials in support of regulatory submissions/registrations per GCP-ICH principles. · ...

This is a Senior Scientist I position that requires leading and executing complex research and development projects from conception through implementation. · ...