Sc & Ec Site Scheduler

**Description**: Are you ready to grow your career and take on a new challenge? Corteva Agriscience has an exciting opportunity for a **Master Scheduler Associate** to join our team in **Supply Chain Southern Cone**. Become part of our team of top-notch supply chain professionals so you can play an important part of leading the agriculture market to seed and...

Freelance - NDT - Mechanical Supplier Name CIRQUE DU SOLEIL Site Address Costanera Sur, Buenos Aires 2230 Avenida Espana 1107 AMP Argentina Equipment Structure metallique - cirque du soleil Type of Inspector Mechanical - NDT Inspection scope Visual verification of different structural components to detect plastic deformations Visual verification of...

Company Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. **Job Description**: Join our international team and be the...

Company Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. **Job Description**: Join our international team and be the...

PPD is a leading global contract research organization. At PPD we are passionate, deliberate, and driven by our purpose - to improve health. Site and Patient Access is a global department working to provide rapid site activation and patient access to our clients. Our innovative approach is designed to help save our clients time and money while driving...

[16:21] Michelle Christophersen As PPD CAS, the following will be the responsabilities: - Prepares, reviews and coordinates, under guidance, local regulatory submissions therapy approvals, viral safety dossiers, import license) in alignment with global submission strategy. - Provides, under guidance local regulatory strategy advice (MoH &/or EC)...

CAS: As PPD CAS, the following will be the responsabilities: - Prepares, reviews and coordinates, under guidance, local regulatory submissions therapy approvals, viral safety dossiers, import license) in alignment with global submission strategy. - Provides, under guidance local regulatory strategy advice (MoH &/or EC) to internal clients. - Provides...

387878BR **Expert Clinical Research Associate**: Argentina **About the role** **Work Model**:Hybrid **Locality**:Buenos Aires **About the Role**: Site relationship management role to ensure sustainable trial execution at Site. Performs on-site and remote monitoring activities related to initiation, conduct and timely completion of Phase I-IV GDD trials...

Company DescriptionPSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.Job Description:Join our international team and be the key...

Primary contact and liaison with investigative sites during study maintenance and -when assigned-, site start-up activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB submissions are made within the timelines agreed with project management and Start-up team. **Labcorp is proud to be...

**ALL CV´s MUST BE SUBMITTED IN ENGLISH IN ORDER TO BE CONSIDERED!** **Essential Functions**: - Assist/Advise project teams on all regulatory requirements for clinical studies - Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings - Review and adapt study specific...

CAS:As PPD CAS, the following will be the responsabilities:Prepares, reviews and coordinates, under guidance, local regulatory submissionstherapy approvals, viral safety dossiers, import license) in alignment with globalsubmission strategy. Provides, under guidance local regulatory strategy advice (MoH &/or EC) tointernal clients. Provides project specific...

100,000. That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations (GCO) touches patients’ lives every day acting as a link between science and medicine. Envision the impact you could have! #GCO Site relationship management role to ensure sustainable trial execution at Site. Performs on-site and remote...

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. With over 19,000 staff...

100,000. That's how many patients participate in our clinical trials at any given time. Global Clinical Operations (GCO) touches patients' lives every day acting as a link between science and medicine. Envision the impact you could have #GCOSite relationship management role to ensure sustainable trial execution at Site. Performs on-site and remote monitoring...

1) Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned 2) Responsible for all aspects of site management as prescribed in the project plans 3) General On-Site Monitoring...

1) Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned2) Responsible for all aspects of site management as prescribed in the project plans3) General On-Site Monitoring...

En Bristol Myers Squibb, nos inspira una sola visión: transformar la vida de los pacientes a través de la ciencia. En oncología, hematología, inmunología y enfermedades cardiovasculares, y una de las líneas de producción más diversas y prometedoras de la industria, cada uno de nuestros apasionados compañeros contribuye a innovaciones que impulsan...

Essential Job Duties: The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...