URGENT OCIR: Senior Clinical Research Associate
The Operating Ceter for INA-RESPOND (OCIR) urgently needed for Senior Clinical Research Associate
Base: Jakarta
Contract Duration 1 (one year) starting in Mid of January 2012
Interesting candidate please send your CV, Certificates, and application letter before Jan 17, 2012 toherman_kosasih@yahoo.com
JOB TITLE: Senior Clinical Research Associate
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. Exercises delegated training and supervisory responsibility for CRA assigned to a specific project. 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 a life sciences program or field; nursing degree preferred but not required
Minimum 1-3 years as a clinical monitor (SQV, SIV,SMV, SCV) independently
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
Base: Jakarta
Contract Duration 1 (one year) starting in Mid of January 2012
Interesting candidate please send your CV, Certificates, and application letter before Jan 17, 2012 toherman_kosasih@yahoo.com
JOB TITLE: Senior Clinical Research Associate
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. Exercises delegated training and supervisory responsibility for CRA assigned to a specific project. 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 a life sciences program or field; nursing degree preferred but not required
Minimum 1-3 years as a clinical monitor (SQV, SIV,SMV, SCV) independently
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
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