Clinical Research Malaysia jobs

Job Description & Requirements

1. Responsible for performing all monitoring aspects of clinical trials and assist to set up, review and maintain project files to ensure compliance as stated in ICH E6 GCP to assure all trials are conducted in strict adherence to good clinical practices, regulatory obligations, investigator integrity and compliance with project specific requirements

2. Responsible for preparing, organizing, managing feasibility, site selection and investigator identification, initiation, monitoring an close-out visits in accordance with sponsor's and/or company's standard operating procedures (SOPs) and study requirements with the highest standards

3. Planning, develop, compile and/or review all study-related regulatory and administrative documents from investigational sites, monitoring visit reports, work progression reports and other study-required documents

4. Develop, compile and/or submit dossiers include initial/amendment/interim report/safety reporting to regulatory and/or ethics committee for review and follow up until approval, as required

5. Management in planning, coordinating, organizing and attending all study-related meetings and activities for sites as required

6. Manage/support project(s) in the capacity of lead CRA role and/or other designated project roles to undertake all or partial responsibilities and tasks as required, whenever designated by the Company

7. Support/Assist in Site and CRO audit or inspection as required

8. Support business development activities (e.g. search new project related information) as required

9. Support/assist in regulatory research/consultancy tasks in relation to clinical trial planning, conduction and product application/registration

10 Proactively identify and facilitate resolution of complex study problems and issues.

11. Actively work towards achieving good personal relationships with the project Team members

Work Experiences, Skills and Personal Qualities

• Minimum 3 years relevant experience in clinical research in healthcare, pharmaceutical and/or CRO industry or is a qualified pharmacist or medical doctor by training with no previous experience in relevant experience in clinical research
• Preferably has experienced in clinical study monitoring
• Good knowledge of medical terminology and clinical/medical practices

This will be a 1 year contract position. More information will be shared during the interview process.

Job Type: Full-time

Pay: RM4,000.00 - RM7,000.00 per month

Benefits:

• Cell phone reimbursement
• Health insurance
• Professional development
• Work from home

Ability to commute/relocate:

• Kuala Lumpur: Reliably commute or planning to relocate before starting work (Required)

Work Location: Hybrid remote in Kuala Lumpur (Kuala Lumpur)