Join our international team and be the key support to clinical research projects as part of the start-up team working in a dynamic multi-functional environment gaining unique skills from various disciplines relevant to clinical research.
You will:
- Facilitate review and negotiation of clinical trial agreements and investigator grants between PSI staff and Israel study sites.
- Customize and prepare contractually binding site-specific documents in cooperation with PSI Legal.
- Prepare the executable version of the contract and coordinate the signature process.
- Update and maintain relevant tracking and filing systems.
- Liaise with project teams and other PSI departments on site contracting and grant negotiation matters.
Qualifications :
- College/University degree or an equivalent combination of education training and experience
- Prior industry experience in clinical research ideally working as Monitor / CRA
- Prior experience with legal documents related to clinical trial sites is a plus
- Full working proficiency in Hebrew and English
- Communication and organizational skills
- Attention to detail and ability to plan multitask and work in a dynamic team environment
Additional Information :
We offer:
- Excellent working conditions
- Extensive training and friendly team
- Competitive salary and benefits package
Take the next step in your clinical research career coordinating a variety of tasks and excelling your communication skills while growing with the company.
Remote Work :
No
Employment Type :
Full-time
Join our international team and be the key support to clinical research projects as part of the start-up team working in a dynamic multi-functional environment gaining unique skills from various disciplines relevant to clinical research.You will:Facilitate review and negotiation of clinical trial ag...
Join our international team and be the key support to clinical research projects as part of the start-up team working in a dynamic multi-functional environment gaining unique skills from various disciplines relevant to clinical research.
You will:
- Facilitate review and negotiation of clinical trial agreements and investigator grants between PSI staff and Israel study sites.
- Customize and prepare contractually binding site-specific documents in cooperation with PSI Legal.
- Prepare the executable version of the contract and coordinate the signature process.
- Update and maintain relevant tracking and filing systems.
- Liaise with project teams and other PSI departments on site contracting and grant negotiation matters.
Qualifications :
- College/University degree or an equivalent combination of education training and experience
- Prior industry experience in clinical research ideally working as Monitor / CRA
- Prior experience with legal documents related to clinical trial sites is a plus
- Full working proficiency in Hebrew and English
- Communication and organizational skills
- Attention to detail and ability to plan multitask and work in a dynamic team environment
Additional Information :
We offer:
- Excellent working conditions
- Extensive training and friendly team
- Competitive salary and benefits package
Take the next step in your clinical research career coordinating a variety of tasks and excelling your communication skills while growing with the company.
Remote Work :
No
Employment Type :
Full-time
View more
View less