|
Romanian Speaking Clinical Research Associate |
| Posted: |
16/05/08 |
 |
| Recruiter: | 1st-itpeople.com |
| Reference: | LYD - 95 |
| Type: | Permanent Vacancy |
| Language: | English, Romanian |
| Salary: | |
| Benefits: | |
| Location: | West Sussex |
| Description: |
PERM: UK Based, International Oncology and Cardio Romanian Speaking Clinical Research Associate - Phase II to IV
Contact Information:
Lee Dunn
Tel: +44 (0) 207 255 6665
Lee.dunn@1st-pharmapeople.com
http://www.1st-pharmapeople.com
Job Summary:
You will be working for a therapeutic area specific global CRO (Oncology and Cardio) on international, complex and multiple site projects. Monitoring and traveling internationally when not working from the office that is 30 minutes from a major UK Airport and London Eurostar connections.
Offers:
This role will offer exposure to complex, multi-centre, international projects in Oncology and Cardio. Internal progression is highlighted along with additional training.
Regular use of mother tongue or additional language skills in a professional capacity with a competitive salary judged on experience and skills. A benefits package is also part of the role. You will work on 2-3 Projects at a time.
Candidates:
Suitable candidates will need to be completely fluent in Romanian and English both written and spoken. You will need a MINIMUM of 6-12 months monitoring experience in Romanian speaking sites.
All candidates will be office based in the UK when not traveling on International projects candidates must already be living in England or moving to England.
A life Science Degree or international equivalent/Nursing degree is essential, the higher the Degree the better.
Driving license's for Romania or England will also be needed to allow for multi-centre visits.
Job Brief:
Your main duties will be to monitor allocated sites to ensure that the monitoring process complies with relevant SOPs, GCP and regulatory requirements.
Contribute to the in-house review of Case Report Form and to perform queries resolution.
Report and follow up on Serious Adverse Events
You will also have to conduct site initiations, start-up and closeout monitoring visits along with preparation and delivery of presentations at investigators meetings.
Manage trip reports, letters, query resolutions and expenses.
Maintain regular communication with the sites, report in writing all sites visits and other contacts, ensuring that the Clinical Project Manager is informed of the study progress and/or any problems with the sites.
All reports to be submitted in English despite the International sites involved.
If you would to discuss this role in greater detail or your application / suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on.
This company is acting as an Agency and/or Employment Business
Clinical Research, CRA, Clinical Research Associate, Study Manager, Study Management, Project Manager, Clinical Study, Clinical Studies, Clinical Trial, Clinical Trials and Clinical Development, Phase, Research Physician, Medical Doctor, ICH GCP, Good Clinical Practice, GCP and Drug Development |
|
|
|        |
