Graduate Research Assistant

3 weeks ago


Seremban, Malaysia International Medical University Full time

**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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