Job Vacancy
“Study Coordinator”
Qualifications as follows :
- Male/ Female maks. 35 years old
- Good Communication
- Self motivated and able to work independence
- Required language(s): English
- At least 1 Year(s) of working experience in the related field is required for this position.
- Preferably Medical Scientific or nurse background.
Job Description:
- Collaborates with the PI to prepare IRB/HRPO and any other regulatory submission documents as required by the protocol.
- Prepares other study materials as requested by the PI. These study materials include, but are not limited to, the informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs.
- Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.
- Reviews and develops a familiarity with the contract or award terms and conditions. Works with the PI to assure that the study is in compliance with all terms and conditions, including but not limited to education, IRB (HRPO) approval, conflict of interest disclosure, health and safety protections for participants and staff and any financial terms or conditions.
Please send your update CV to netty.manurung@kalbe.co.id
“Study Coordinator”
Qualifications as follows :
- Male/ Female maks. 35 years old
- Good Communication
- Self motivated and able to work independence
- Required language(s): English
- At least 1 Year(s) of working experience in the related field is required for this position.
- Preferably Medical Scientific or nurse background.
Job Description:
- Collaborates with the PI to prepare IRB/HRPO and any other regulatory submission documents as required by the protocol.
- Prepares other study materials as requested by the PI. These study materials include, but are not limited to, the informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs.
- Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.
- Reviews and develops a familiarity with the contract or award terms and conditions. Works with the PI to assure that the study is in compliance with all terms and conditions, including but not limited to education, IRB (HRPO) approval, conflict of interest disclosure, health and safety protections for participants and staff and any financial terms or conditions.
Please send your update CV to netty.manurung@kalbe.co.id
