Intern Clinical Research Associate

2 days ago

Singapore MSD Full time

This Intern position under the oversight of the line-manager will have interfaces with across the different specific roles within the Global Clinical Trial Operations of Malaysia-Singapore Team.

The Intern will be involved in the process of supporting administratively, the conduct of clinical trials for novel therapies at the country level.

Assignment Scope & Learning Opportunities:
(Under the guidance)
- Rotational Assignment for an overview and supporting the roles of Clinical Trial Coordinator, Clinical Operations Manager, and Clinical Research Associate.
- Perform tasks as assigned which may include but not limited to; document management, regulatory and site start-up, clinical drug shipments, ancillary supplies shipments, dashboards/metrics reporting analysis, meeting planning, and other tasks as appropriate.
- Overview into Clinical Trial Systems:

- Clinical Trial Management System - SPECTRUM
- electronic Trial Master Files (eTMF) and supporting administratively with document management where appropriate.
- Dashboards and Reporting
- Other systems as appropriate
- Support the submission of regulatory and ethics submissions of clinical trials. - Understanding Site Ready:

- Coordinates & manages various tasks in collaboration with other roles to achieve Site Ready. Includes: The process of starting up a clinical trial across Malaysia-Singapore, Regulatory Documents Collection, Review, Approval and Maintenance

**Competency Expectations**:
Tertiary degree in relevant areas e.g. healthcare, biosciences, pharmacy, etc
- Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand technical information. Developing ability to present technical information with support.
- General awareness of clinical trial environment and drug development process
- Good attention to detail
- The intern will be trained online and well as on
- the -job to appreciate the role of: Clinical Research Associate and Clinical Trial Coordinator.

**Behavioural Competency Expectations**:

- Effective time management, organizational and interpersonal skills, conflict management
- Able to work with other experienced research professions to develop skills across multiple protocols, sites and therapy areas.
- High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment, with support from Line Manager
- Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships.
- Demonstrates commitment to Customer focus.

**Search Firm Representatives Please Read Carefully**

**Employee Status**:
Intern/Co-op (Fixed Term)

**Relocation**:
**VISA Sponsorship**:
**Travel Requirements**:
**Flexible Work Arrangements**:
**Shift**:
**Valid Driving License**:
**Hazardous Material(s)**:
**Requisition ID**:R253740

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