Fsp - 30+ ofertas

Thermo Fisher Scientific

*Work Schedule** Standard (Mon-Fri) *Environmental Conditions** Office Join Us as an Associate Feasibility Manager - Make an Impact at the Forefront of Innovation The Associate Feasibility Manager leads the setup, survey programming, securing of resources and overall conduct for allocated feasibilit

Parexel FSP is looking for Global Study Managers in Argentina, Brazil or Mexico! Job Summary The Global Study Manager II (GSM II) provides operational leadership throughout the study lifecycle, with accountability for oversight and execution of study management, site management, preferred Contract R

*This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.** *Work Schedule** Standard (Mon-Fri) *Environmental Conditions** Office *Job Description** Join Us

*This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.** *Work Schedule** Standard (Mon-Fri) *Environmental Conditions** Office *Job Description** Join Us

*This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.** *Work Schedule** Standard (Mon-Fri) *Environmental Conditions** Office *Job Description** Join Us

*Work Schedule** Standard (Mon-Fri) *Environmental Conditions** Office *Job Description** Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700

*Work Schedule** Standard (Mon-Fri) *Environmental Conditions** Office *Job Description** Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning

*Work Schedule** Standard (Mon-Fri) *Environmental Conditions** Office *Job Description** Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700

**Job Summary** The **Clinical Scientist (CS)**will provide of observational study execution including epidemiological, non-interventional, pragmatic and low-interventional studies and research collaborations to ensure consistency of approach, conduct, monitoring, analysis, reporting, and oversight

**Parexel FSP is looking for a Quality Project Manager. This is a remote position in Brazil, Argentina OR Mexico. ** **JOB**SUMMARY** The Project Manager is responsible for owning and driving the tactical management and pull-through of operational resources including planning, managing and supportin

The Issue Lead will be responsible for driving QE case management, ensuring that investigations are conducted thoroughly within timelines and compliance requirements, overseeing the efficiency of the process by which the Sponsor conducts GCP investigations, and leveraging data to assess the efficien

Support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by either the agreed algorithm or the Sponsor's requirements, including pre-award activities. **Essential Functions** - Develop simple investigator grant estim

Parexel is looking for a Senior Site Intelligence Specialist in Mexico! The** Senior Site Intelligence Specialist (SIS)** acts as a supportive team member for Regional Intelligence. Performs tasks for multiple Site Intelligence and Feasibility projects. Works under close supervision of Regional Inte

JOB RESPONSIBILITIES As the training development lead, manage courseware development including course design, publishing, testing and deployment. Provide technical, instructional design and operational management for programs and be accountable for meeting project commitments. Communicate and ensure

**Position Overview** The **MLR Facilitator** is responsible supporting MLR (Medical, Legal & Regulatory) content approval process, for system governance, quality assurance, and cross-collaboration support for the FUSE Digital Asset Management (DAM) system. This role serves as a critical link betwee

Manage the Clinical Medical Controlled document (CMCD) process and procedural document portal (relational database that includes business process modeling and allows for management of controlled documents and associated information with an end user interface which provides the business access to int

**Please, make sure to upload your updated CV in English. **: **Overview**: The Analytical Monitor is an individual contributor role that supports the execution of analytical monitoring activities that will enable Site Managers to perform guided issue/ risk management. The Analytical Monitor support

**Please, make sure to upload your updated CV in English. **: **Overview**: The Analytical Monitor is an individual contributor role that supports the execution of analytical monitoring activities that will enable Site Managers to perform guided issue/ risk management. The Analytical Monitor support

**JOB SUMMARY** **ROLE RESPONSIBILITIES** General: - Assist the manager implement global strategies, initiatives, processes, and standards to ensure consistent, efficient, and quality processes to meet quality, timelines and deliverables. - Assist to set up and test study level Risk-based Monitoring

**JOB SUMMARY** **RESPONSIBILITIES** General: - Implement global strategies, initiatives, processes, and standards to ensure consistent, efficient, and quality processes to meet quality, timelines and deliverables. - Provide technical expertise to set up and test study level Risk-based Monitoring sy