The Operating Center for INA-RESPOND (OCIR)

The Operating Center for INA-RESPOND (OCIR) urgently needed

Base: Jakarta Contract Duration 1 (one year) starting in Mid of January 2012

POSITION TITLE :

1. Senior Clinical Research Associate/Clinical Research Monitor

FUNCTION: Responsible for performing and coordinating all monitoring strategies for clinical research studies for the Indonesia Research Partnership in Infectious Disease (lNA-RESPOND) Operation Center in Jakarta, Indonesia. Conducts site qualification(SQV) site initiation( SlV),site monitoring (SMV) and site close-out visits(SCV) to determine protocol and regulatory compliance. Assure compliance with the GCP,ICH and SOPs.

Provides administrative operational and procedural support to coordinate and guide protocol teams (investigators and scientific/technical experts) through protocol development, review and implementation processes. Drafts protocol and protocol support documents including manuals of procedures informed consent forms, clarification memos and training materials.

DUTIES AND RESPONSIBILITIES

1. Clinical Research Monitoring

2. Clinical Research Protocol Project Management

QUALIFICATIONS:

Education and/or Experience:

S1 in biology, medical doctor or nursing Minimum 1-3 years as a CLINICAL MONITOR IN A CLINICAL STUDY is a must (SQV, SIV,SMV, SCV)

Knowledge/ skills/ Other Requirements

. Written and verbal fluency in English and Bahasa Indonesia

. Excellent communication skills (written and verbal) with the ability to communicate effectively with clinical site staff

POSITION TITLE :

2. Clinical Research site Specialist

Job Description:

Manage and provide a range of clinical research support activities for the Indonesia Research partnership on Infectious Disease (INA-RESPOND) Operation Center in Jakarta, Indonesia. Duties include but are not limited to: provide clinical research site training and support for protocol implementation and site development activities; conduct site visits; conduct quality management activities, manage work with other members of the operation center to ensure that all protocol related activities are completed according to client timelines; provide support to the protocol development team; conduct review of protocol documents; assist with development of project budgets; serve as data manager. Candidate must be comfortable working in a fast-paced environment and must be fluent in Indonesian and English

DUTIES AND RESPONSIBILITIES

1. Site Liaison

2. Site Assessment and Preparedness Evaluation

3. Training: Plan, coordinate and help conduct clinical research site staff training (e.g. GCP)

4. Data Management: responsible for CRF

5. Protocol Development and Implementation

QUALIFICATIONS:

Education and/or Experience:

A medical doctor; master degree in public health, biomedic or microbiology is preferred but not required

Minimum 1-3 years medical research experience

Knowledge/ skills/ Other Requirements

. Written and verbal fluency in English and Bahasa Indonesia

. Excellent communication skills (written and verbal) with the ability to communicate effectively with clinicians and investigators

Interesting candidate please send your CV, Certificates, and application letter before Jan 17, 2012 to herman_kosasih@yahoo.com