Clinical Trial Project Specialist #HCK

RECRUIT EXPRESS PTE LTD

Singapore

On-site

SGD 60,000 - 90,000

Full time

14 days+

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Job summary

RECRUIT EXPRESS PTE LTD in Singapore is seeking an experienced professional to oversee the full study lifecycle from planning to closeout. You will act as the primary liaison between sponsors, ethics boards, and monitors to ensure protocol feasibility and compliance.

The role requires a degree in Nursing, Science, Health, or Management and at least five years of clinical research experience with strong knowledge of GCP and trial processes.

Qualifications

Minimum 5 years of clinical research experience.
Strong knowledge of GCP and clinical trial processes.

Responsibilities

To oversee full study lifecycle from planning to closeout.
To act as primary liaison between the clinical research sponsors ethics boards, and monitors.
To lead protocol development to ensure operational feasibility.
To manage study documents, risk mitigation, safety oversight, and trial master files.
To coordinate study timelines, vendor engagement, training and logistics
To Track budgets and provide regular study updates to stakeholders.
To Coordinate monitoring visits and resolve data queries and quality issues.

Skills

Clinical research experience

GCP knowledge

Education

Degree in Nursing, Science, Health, or Management

Job description

Responsibilities

To oversee full study lifecycle from planning to closeout.
To act as primary liaison between the clinical research sponsors ethics boards, and monitors.
To lead protocol development to ensure operational feasibility.
To manage study documents, risk mitigation, safety oversight, and trial master files.
To coordinate study timelines, vendor engagement, training and logistics
To Track budgets and provide regular study updates to stakeholders.
To Coordinate monitoring visits and resolve data queries and quality issues.

Qualification

Degree in Nursing, Science, Health, or Management.