Dan lowongan yang pakai email gratisan bisa lihat di sini, lebih hati-hati mengirimkan CV-nya yah, ga tau seperti contoh SCAM di sini or bukan :(
Bekerja salah satu tujuannya adalah untuk beribadah, maka carilah tempat ibadah yang cukup baik :)
Karena batasan dari Blogger cuma 50 posting/hari, maka gw buat blog lanjutannya di sini.

Jul 6, 2008

Fw: http://www.jobislands.net Vacancy : Junior Clinical Research Associate - Clinical Research Associate @ GleneaglesCRC]

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From: "Fabiola Hutabarat" <mimosa@uninet.net.id>
Date: Tue, 1 Jul 2008 11:15:48 +0700 (WIT)
To: undisclosed-recipients:;<Invalid address>
Subject: http://www.jobislands.net Vacancy : Junior Clinical Research Associate - Clinical Research Associate @ GleneaglesCRC]

1 July 2008

Dear All,

Our company, GleneaglesCRC, a Singapore-based contract research
organization, is currently looking for a Junior Clinical Research
Associate and Clinical Research Associate to be posted in our Indonesia
office. The job details and
qualification are as follow :

Reports To :
Clinical Research Manager

General Description :
The Junior Clinical Research Associate and Clinical Research Associate is
responsible for the
administration, management of clinical studies and ensures quality and
timeliness of clinical trials.

Roles and Responsibilities :
Together with Clinical Research Manager/Project Manager performs the
following :
1. To establish and implement project plans
2. To meet clinical trials operational and financial standards
3. To identify investigators for projects
4. To prepare and submit dossiers for Ethics Committee and Regulatory
approval
5. To train site staff on project-specific issues
6. To ensure protocol compliance, ICH-GCP, and other regulatory
obligations at trial sites
7. To verify the accuracy and authenticity of clinical data
8. To ensure that timely reporting of study information, which includes
safety reporting to relevant study team member and regulatory authorities
9. To manage investigational products and other trial-related supplies
10. To manage quality data
11. To maintain adequate clinical trial documentation
12. To prepare monitoring reports
13. To plan and implement recruitment strategies
Perform other related duties as assigned

Qualification :
Registered Nurse, Graduate Degree in Life Sciences or Pharmacy

Experience :
Minimum of 1 year clinical research experience

Skills :
- At least 1 year of clinical trials experience required
- Knowledge of ICH-GCP required
- Possess a breadth of clinical knowledge and medical terminology
- Good interpersonal, written and verbal communication skills
- Fluent in English, both written and verbal
- Good research and computer skills preferred
- Attention to details, teamwork, process improvement, analyzing information
- Mature and independent with the ability to work with a team
- Willing to travel 3-50 days a year
- Adaptable and have the ability to work under a wide variety of conditions

Should you meet the above requirements and interested in this position,
please send your cover letter and curriculum vitae (both in English),
together with your latest photograph to : fabiola_rh@gleneaglescrc.com

Only shortlisted candidates will be called for interview.

Thank you.

Best Regards,

Fabiola C. R. Hutabarat

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