Project Support Coord - Ciudad de México - Thermo Fisher Scientific
Descripción
We are vital links between an idea for a new medicine and the people who need it.We are the people of PPD - thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health.
You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients.
Our clinical department defines, develops and delivers clinical programmes, ensuring the highest-quality review of data and effective interaction with study sites.
As a Clinical Trial Coordinator, you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract.
Additionally key responsibilities include:
- Performs PPD Investigator file reviews and logging of outstanding issues in project related tracking tools
- Reviews regulatory documents for proper content
- Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified
- Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
- Assists with the identification of potential investigators and development/distribution of initial protocol packets
- Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes
We are the people of PPD - thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health.
You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients.
Our clinical department defines, develops and delivers clinical programmes, ensuring the highest-quality review of data and effective interaction with study sites.
As a Clinical Trial Coordinator, you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract.
Additionally key responsibilities include:
- Performs PPD Investigator file reviews and logging of outstanding issues in project related tracking tools
- Reviews regulatory documents for proper content
- Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified
- Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
- Assists with the identification of potential investigators and development/distribution of initial protocol packets
- Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes
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