Site Activation Lead (Hybrid)

IQVIA; Singapore; Hybrid; SGD 70,000 - 90,000; Full time

Job summary

A global clinical research provider in Singapore is seeking a Clinical Project Lead to ensure the quality and adherence to timelines of assigned studies. This role requires strong regulatory knowledge, contract negotiation skills, and the ability to manage internal databases. Ideal candidates should have a Bachelor's in life sciences and at least 3 years of relevant experience. The position offers a hybrid work model.

Qualifications

• 3 years’ clinical research or relevant experience.
• Ability to apply applicable regulatory guidelines.
• Understanding of regulated clinical trial environment.

Responsibilities

• Serve as SPOC in assigned studies for investigative sites.
• Perform Regulatory, Start-up and Maintenance activities.
• Prepare and review site regulatory documents.
• Negotiate site contracts and budgets.
• Ensure accuracy of internal systems and databases.
• Review site performance metrics.
• Establish project planning and timelines.
• Contribute to regulatory intelligence collection and analysis.

Skills

In-depth knowledge of clinical systems

Good negotiating skills

Effective communication

Organizational skills

Ability to work independently

Knowledge of GCP/ICH guidelines

Education

Bachelor’s Degree in life sciences or related field

Job description

A global clinical research provider in Singapore is seeking a Clinical Project Lead to ensure the quality and adherence to timelines of assigned studies. This role requires strong regulatory knowledge, contract negotiation skills, and the ability to manage internal databases. Ideal candidates should have a Bachelor's in life sciences and at least 3 years of relevant experience. The position offers a hybrid work model.