- Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study.
- Verifies that the rights and well-being of human subjects clinical studys participants are protected and conducts monitoring to confirm subject safety and data integrity.
- Acts as the main point of communication with Investigator and site team; documents conducted communication as per the study specific guidelines.
- Trains investigational site staff as necessary.
- Participates in feasibility studies for new projects as required.
- Supports preparation of regulatory and / or EC submissions
- Supports site contracting in the specific country.
Qualifications :
- College/University degree in Life Sciences
- Extensive on-site monitoring experience with experience of complex trials in oncology or rare disease
- Experience in SSU & Site Contracts
- Ability to plan multitask and work in a dynamic team environment
- Communication collaboration and problem-solving skills
- Full working proficiency in English
- Ability to travel nationally with a valid driving license
Additional Information :
Our core values are key to how we operate and if you feel they resonate with you then Ergomed is a great company to join!
Quality
Integrity & Trust
Drive & Passion
Agility & Responsiveness
Belonging
Collaborative Partnerships
We look forward to welcoming your application.
Remote Work :
Yes
Employment Type :
Full-time
Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study.Verifies that the rights and well-being of human subjects clinical studys participant...
- Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study.
- Verifies that the rights and well-being of human subjects clinical studys participants are protected and conducts monitoring to confirm subject safety and data integrity.
- Acts as the main point of communication with Investigator and site team; documents conducted communication as per the study specific guidelines.
- Trains investigational site staff as necessary.
- Participates in feasibility studies for new projects as required.
- Supports preparation of regulatory and / or EC submissions
- Supports site contracting in the specific country.
Qualifications :
- College/University degree in Life Sciences
- Extensive on-site monitoring experience with experience of complex trials in oncology or rare disease
- Experience in SSU & Site Contracts
- Ability to plan multitask and work in a dynamic team environment
- Communication collaboration and problem-solving skills
- Full working proficiency in English
- Ability to travel nationally with a valid driving license
Additional Information :
Our core values are key to how we operate and if you feel they resonate with you then Ergomed is a great company to join!
Quality
Integrity & Trust
Drive & Passion
Agility & Responsiveness
Belonging
Collaborative Partnerships
We look forward to welcoming your application.
Remote Work :
Yes
Employment Type :
Full-time
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