Contract Clinical Study Assistant | US Pharma MNC | 5 Days Office Hours #HCT

Recruit Express Pte Ltd; Singapore; Sur place; SGD 31 000 - 40 000; Plein temps

Résumé du poste

Recruit Express Pte Ltd in Singapore is seeking a Clinical Study Assistant to support clinical study operations and ensure smooth coordination and documentation of activities.

You will provide admin support, maintain study files, track timelines, and liaise with internal teams to drive compliance and efficient study progress.

Qualifications

• Diploma/Degree in Life Sciences, Biomedical Science, Pharmaceutical Science, Nursing or related discipline.
• Candidates with clinical research/study coordination experience will have an advantage.

Responsabilités

• Provide administrative and coordination support for clinical studies.
• Assist in the preparation, tracking and maintenance of study documents.
• Coordinate study-related meetings, documentation and correspondence.
• Maintain accurate clinical study files and records.
• Track study timelines, documents and outstanding action items.
• Liaise with internal study teams and relevant stakeholders.
• Assist with data entry, filing and other study-related administrative duties.
• Ensure documentation is maintained accurately and in accordance with internal procedures.

Formation

Diploma/Degree in Life Sciences, Biomedical Science, Pharmaceutical Science, Nursing or related discipline

Description du poste

Looking to build your career in Clinical Research with a reputable US Pharmaceutical MNC?

We are looking for a Clinical Study Assistant to support clinical study operations and work closely with the study team in ensuring smooth coordination and documentation of clinical research activities.

Job Highlights

• US Pharmaceutical MNC
• 5-day work week
• Office hours
• Excellent exposure to clinical research and study operations
• Good opportunity for candidates looking to build a career within the pharmaceutical industry

Key Responsibilities

• Provide administrative and coordination support for clinical studies
• Assist in the preparation, tracking and maintenance of study documents
• Coordinate study-related meetings, documentation and correspondence
• Maintain accurate clinical study files and records
• Track study timelines, documents and outstanding action items
• Liaise with internal study teams and relevant stakeholders
• Assist with data entry, filing and other study-related administrative duties
• Ensure documentation is maintained accurately and in accordance with internal procedures

Requirements

• Diploma/Degree in Life Sciences, Biomedical Science, Pharmaceutical Science, Nursing or related discipline
• Candidates with clinical research/study coordination experience will have an advantage