We are currently looking for a Clinical Research Associate for one of the top players in the pharmaceutical industry, with a legacy of more than 68 years in Malaysia. This position requires your urgent attention.
...
- Reporting to: Clinical Manager
- Location: Kuala Lumpur
- Excellent employee compensation and benefits
- Work Type: Hybrid
the role
- Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock.
- Contributes to Case Report Form (CRF) design and clinical trial document development as they pertain to clinical monitoring activities (i.e., operating manuals, monitoring guidelines, etc.)
- Involved in recruitment of potential Investigators, preparation of Independent Ethics Committee/ Independent Regulatory Board (IEC/IRB) submissions, notifications to regulatory authorities, translation of study related documentation, organization of meetings and other tasks as instructed by the Project Manager.
- Negotiates investigator budgets and assists with the execution of site contracts with support from the legal department.
- Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports.
the experience
- Bachelor’s degree in nursing or biomedical sciences or pharmacy, MBBS/MD with clinical experience will also be considered
- At least 2 years of relevant working experience in clinical research and handling clinical trials
- GCP Certification
- Resourceful, analytic and able to work under pressure
how to apply
Please apply directly to the link. Alternatively, please contact Brendan at 0134130410 if you are interested in the job.
show more
We are currently looking for a Clinical Research Associate for one of the top players in the pharmaceutical industry, with a legacy of more than 68 years in Malaysia. This position requires your urgent attention.
- Reporting to: Clinical Manager
- Location: Kuala Lumpur
- Excellent employee compensation and benefits
- Work Type: Hybrid
the role
- Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock.
- Contributes to Case Report Form (CRF) design and clinical trial document development as they pertain to clinical monitoring activities (i.e., operating manuals, monitoring guidelines, etc.)
- Involved in recruitment of potential Investigators, preparation of Independent Ethics Committee/ Independent Regulatory Board (IEC/IRB) submissions, notifications to regulatory authorities, translation of study related documentation, organization of meetings and other tasks as instructed by the Project Manager.
- Negotiates investigator budgets and assists with the execution of site contracts with support from the legal department.
- Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports.
the experience
- Bachelor’s degree in nursing or biomedical sciences or pharmacy, MBBS/MD with clinical experience will also be considered
- At least 2 years of relevant working experience in clinical research and handling clinical trials
- GCP Certification
- Resourceful, analytic and able to work under pressure
...
how to apply
Please apply directly to the link. Alternatively, please contact Brendan at 0134130410 if you are interested in the job.
show more