Back to search.SEC Recruitment Ltd - Clinical Research Associate
| Employment Type: | Permanent |
| Location: | Germany |
| Salary: | negotiable depends on experience |
| Languages: | English |
Are you a CRA who worked in early phases of Clinical Development? Do you have good English and would you like to work from home? Sounds like something that you were thinking of and would be willing to do? Well, our client is a leading global drug development company known for its excellence in the market place. As a result of rapid expansion a highly valued position CRA or Monitor has become available.
Your principal responsibilities include but not limited to:
Provision of feasibility, site initiation, selection, monitoring and close out visits for clinical studies. You will conduct full cycle of CRA activities in compliance with international ICH/GCP standards and will extensively use SOP regulations. Being involved in liaison with investigators and sponsors you will be responsible for reporting on all protocol or ad hoc related issues to your project/line manager.
Your profile:
Degree in life science or/and medicine or extensive experience in clinical research. Demonstrated experience in monitoring of Clinical Studies (Phase I) and ability to work together with other departments and project teams in the region and across Europe. Strong PC skills with Microsoft Applications. Knowledge of ICH guidelines. Excellent presentation and communication skills will be required to provide liaison at all levels internally and externally. Fluency in English is essential. Additional European language would be an advantage. Ability to travel up to 80% is required. This role involves a high level of flexibility. If for some reason this position is not of interest for you but you know someone suitable there is a bonus fee of EUR250 for every referred candidate that we successfully place.
In return our client will offer excellent career progression opportunities, competitive salary and remuneration package and an enviable working environment.
For immediate consideration please forward your CV to roman.treydin@secpharma.com or call +44 207 255 6600 for further information
Your principal responsibilities include but not limited to:
Provision of feasibility, site initiation, selection, monitoring and close out visits for clinical studies. You will conduct full cycle of CRA activities in compliance with international ICH/GCP standards and will extensively use SOP regulations. Being involved in liaison with investigators and sponsors you will be responsible for reporting on all protocol or ad hoc related issues to your project/line manager.
Your profile:
Degree in life science or/and medicine or extensive experience in clinical research. Demonstrated experience in monitoring of Clinical Studies (Phase I) and ability to work together with other departments and project teams in the region and across Europe. Strong PC skills with Microsoft Applications. Knowledge of ICH guidelines. Excellent presentation and communication skills will be required to provide liaison at all levels internally and externally. Fluency in English is essential. Additional European language would be an advantage. Ability to travel up to 80% is required. This role involves a high level of flexibility. If for some reason this position is not of interest for you but you know someone suitable there is a bonus fee of EUR250 for every referred candidate that we successfully place.
In return our client will offer excellent career progression opportunities, competitive salary and remuneration package and an enviable working environment.
For immediate consideration please forward your CV to roman.treydin@secpharma.com or call +44 207 255 6600 for further information
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