- Carries out assigned administrative duties to support clinical trial conduct
- Sets up Investigator Site File according to SOPs provided either by the Sponsor or by ERGOMED and distribute to sites
- Coordinates and attends project meetings (e.g. investigator kick-off team etc.) with the PM/CTM. Supports preparation of meeting agenda and provides written high-quality meeting minutes within specified timeframe
- Works with project teams to assist in tracking naming and routing of clinical trial documentation to the Trial Master File (TMF)
- Maintains contact lists information for project team members (e.g. project training records) and other trackers as required. Provides reports from tracking tools.
- If requested attends in-house audits and supports completion of Corrective and Preventative Action Plan
- Any other task related to the specific clinical trial performance
Qualifications :
- High school diploma or equivalent or adequate experience in the field of clinical research
Additional Information :
Why PrimeVigilance
We prioritize diversity equity and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds genders and ages can contribute and grow.
To succeed we must work together with a human first approach. Why because our people are our greatest strength leading to our continued success on improving the lives of those around us.
We offer:
Strong emphasis on personal and professional growth
Friendly supportive working environment
Opportunity to work with colleagues based all over the world with English as the company language
Our core values are key to how we operate and if you feel they resonate with you then PrimeVigilance could be a great company to join!
Quality
Integrity & Trust
Drive & Passion
Come and join us in this exciting journey to make a positive impact in patients lives. We look forward to welcoming your application.
Remote Work :
No
Employment Type :
Full-time
Carries out assigned administrative duties to support clinical trial conductSets up Investigator Site File according to SOPs provided either by the Sponsor or by ERGOMED and distribute to sitesCoordinates and attends project meetings (e.g. investigator kick-off team etc.) with the PM/CTM. Supports p...
- Carries out assigned administrative duties to support clinical trial conduct
- Sets up Investigator Site File according to SOPs provided either by the Sponsor or by ERGOMED and distribute to sites
- Coordinates and attends project meetings (e.g. investigator kick-off team etc.) with the PM/CTM. Supports preparation of meeting agenda and provides written high-quality meeting minutes within specified timeframe
- Works with project teams to assist in tracking naming and routing of clinical trial documentation to the Trial Master File (TMF)
- Maintains contact lists information for project team members (e.g. project training records) and other trackers as required. Provides reports from tracking tools.
- If requested attends in-house audits and supports completion of Corrective and Preventative Action Plan
- Any other task related to the specific clinical trial performance
Qualifications :
- High school diploma or equivalent or adequate experience in the field of clinical research
Additional Information :
Why PrimeVigilance
We prioritize diversity equity and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds genders and ages can contribute and grow.
To succeed we must work together with a human first approach. Why because our people are our greatest strength leading to our continued success on improving the lives of those around us.
We offer:
Strong emphasis on personal and professional growth
Friendly supportive working environment
Opportunity to work with colleagues based all over the world with English as the company language
Our core values are key to how we operate and if you feel they resonate with you then PrimeVigilance could be a great company to join!
Quality
Integrity & Trust
Drive & Passion
Come and join us in this exciting journey to make a positive impact in patients lives. We look forward to welcoming your application.
Remote Work :
No
Employment Type :
Full-time
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