Vissza a kereséshez.SEC Recruitment Ltd - CLINICAL RESEARCH ASSOCIATE II
| Foglalkoztatási típus: | Permanent |
| Hely: | Hungary |
| Fizetés: | NEGOTIABLE |
| Idegennyelvek: | Angol, Magyar |
My client is a leading international CRO in Hungary and currently is looking for a Clinical Research Associate II (CRA II) with strong experience in monitoring the clinical trials, ready for a challenging job in an international organisation. The successful applicant will have the opportunity to work on varied projects, therapeutic areas and phases of development. This is a full-time, office based position.
Challenges:
The responsibility of a Clinical Research Associate II (CRA II) is to perform the full clinical monitoring aspect of the assigned projects in accordance with Company's SOPs and GCP. The duties will span from feasibility visits, pre-study and study initiation visits, through the preparation of the concise reports of monitoring visits to performing the close-out activities in compliance with regulatory requirements. Overall you will ensure the completeness and accuracy of all study aspects, submit RA and EC submission documentation, coordinate all study material and site related study documentation. Additionally, you will assess, monitor and train study site staff as required.
Experience
Ideally you will have a degree in Medicine or Pharmacy and cardiovascular experience but other life science degree (biology, physical or health studies, nursing degree) is acceptable with at least 2 years monitoring experience. You will have a thorough understanding of clinical research principles and processes, and will be able to work diligently and methodically. You will have strong interpersonal skills and be a team player. Additionally, you will posses excellent planning and organisational skills with effective time management and exceptional oral and written communication skills both in Hungarian and English language.
If you are interested in this opportunity or know somebody who might be suitable/interested, please feel free to contact me or pass my contact details for further information.
To apply please send your CV to Matus.Hlivjak@secpharma .com or contact me on 0044 207 255 6600 for additional information.
Challenges:
The responsibility of a Clinical Research Associate II (CRA II) is to perform the full clinical monitoring aspect of the assigned projects in accordance with Company's SOPs and GCP. The duties will span from feasibility visits, pre-study and study initiation visits, through the preparation of the concise reports of monitoring visits to performing the close-out activities in compliance with regulatory requirements. Overall you will ensure the completeness and accuracy of all study aspects, submit RA and EC submission documentation, coordinate all study material and site related study documentation. Additionally, you will assess, monitor and train study site staff as required.
Experience
Ideally you will have a degree in Medicine or Pharmacy and cardiovascular experience but other life science degree (biology, physical or health studies, nursing degree) is acceptable with at least 2 years monitoring experience. You will have a thorough understanding of clinical research principles and processes, and will be able to work diligently and methodically. You will have strong interpersonal skills and be a team player. Additionally, you will posses excellent planning and organisational skills with effective time management and exceptional oral and written communication skills both in Hungarian and English language.
If you are interested in this opportunity or know somebody who might be suitable/interested, please feel free to contact me or pass my contact details for further information.
To apply please send your CV to Matus.Hlivjak@secpharma .com or contact me on 0044 207 255 6600 for additional information.
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