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Graduate Research Assistant
3 weeks ago
**Study Title**:
Prospective Study on The Maternal and Foetal-neonatal Outcomes of Dengue Infection in Pregnancy
**Study Planning and Implementation**:
- Collaborate with principal investigators and research teams to develop and refine the study protocol.
- Coordinate and facilitate the initiation of the study, including obtaining necessary approvals from ethics committees and regulatory bodies.
**Participant Recruitment and Informed Consent**:
- Develop and implement strategies for participant recruitment, ensuring adherence to inclusion and exclusion criteria.
- Obtain informed consent from pregnant women willing to participate in the study.
**Data Collection and Monitoring**:
- Oversee the collection of clinical and demographic data from study participants.
- Implement standardized data collection procedures and ensure data accuracy and completeness.
- Monitor participant enrollment, ensuring it aligns with study timelines and goals.
**Clinical Assessments**:
- Coordinate clinical assessments and examinations for pregnant women participating in the study.
- Work closely with healthcare providers to schedule and conduct necessary clinical evaluations.
**Sample Collection and Processing**:
- Oversee the collection, processing, and storage of biological samples (e.g., blood, urine) from study participants.
- Ensure compliance with standardized protocols for sample handling and transportation.
**Adverse Event Reporting**:
- Monitor and report adverse events promptly, following established reporting procedures.
- Collaborate with healthcare providers to manage any adverse events that may arise during the study.
**Quality Assurance and Compliance**:
- Implement quality assurance measures to ensure study procedures adhere to regulatory and ethical standards.
- Ensure compliance with Good Clinical Practice (GCP) guidelines and other relevant regulations.
**Communication and Collaboration**:
- Maintain effective communication channels with study investigators, healthcare providers, and other relevant stakeholders.
- Collaborate with other study coordinators, nurses, and support staff to streamline study activities.
**Documentation and Record-Keeping**:
- Maintain accurate and detailed records of study-related activities, including participant data, regulatory documentation, and correspondence.
**Training and Education**:
- Provide training to study staff, healthcare providers, and other relevant personnel involved in the study.
- Ensure that all team members are knowledgeable about the study protocol and procedures.
**Budget Management**:
- Work within the allocated budget for the study, ensuring efficient use of resources.
**Job Types**: Full-time, Contract
Contract length: 36 months
Pay: RM2,300.00 - RM2,600.00 per month
**Benefits**:
- Professional development
Schedule:
- Day shift
- Monday to Friday
Ability to commute/relocate:
- Seremban: Reliably commute or planning to relocate before starting work (required)
**Education**:
- Bachelor's (required)
**Language**:
- Malay (required)
- English (required)
Expected Start Date: 06/03/2024
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