Project Manager - Inscuinatoyac

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 ...

The Associate Project Manager drives and owns a sub-set of project-specific activities as directed by the Project Lead. Additionally, the Associate Project Manager may provide ownership related to the compilation tasks related to supporting overall delivery of the project (qualit ...

The Senior Digital Program/Project Manager is accountable for end-to-end delivery of prioritized digital initiatives that improve throughput, quality, compliance effectiveness, and cost through the DPD Practical Process Improvement (PPI) system and scalable digital solutions. · M ...

As an IT Project Manager you will oversee the planning execution and successful completion of various projects. You will work closely with cross-functional teams to ensure projects are delivered on time and within scope and budget. · ...

The Program Manager is responsible for managing enterprise level programs or collections of related projects within a single business line (technology and non-technology efforts). · ...

The Enterprise Program Manager is responsible for managing enterprise level programs or collections of related projects within a single business line (technology and non-technology efforts). The Program Manager develops the project/program execution strategy in partnership with v ...

Join Us as an Associate Manager Clinical Operations - Make an Impact at the Forefront of Innovation. · The Associate Manager Clinical Operations oversees the daily line management responsibilities of the assigned team.This role serves as a positive leadership and professional rol ...

+ Job summary · Clinical Data Team Lead at Thermo Fisher Scientific: Join our FSP Data Management team and help bring life-changing medicines to patients worldwide. · + Qualifications · • Bachelor's degree or equivalent and relevant formal academic · + Responsibilities · • Applie ...

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 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. · ...

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 ...

Provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. Acts as backup program manager. · ...

Join Us as a Site Payments Associate II - Reconciliation Make an Impact at the Forefront of InnovationAs a Site Payments Associate II - Reconciliation, you will provide administrative, reporting, contractual and financial support to the department related to the processing of pay ...

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 ...

Are you ready to advance your career with an outstanding opportunity? As a Clinical Trial Coordinator at Thermo Fisher Scientific, you will play a vital role in our research efforts located in Argentina. · ...

Maintains relationships with key internal and external clients. Initial communication point, and owns all client communication, gather complex client requirements, and triage incoming opportunities/projects. · ...

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

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. · ...

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. · As an Associate Research Scientist you will perform complex laboratory analysis of pharmaceutical products, · ...