Clinical Research Associate II/ Senior Clinical Research Associate

Icon Clinical Research Hong Kong Limited; Hong Kong; Vor Ort; HKD 420.000 - 660.000; Vollzeit

Benefits dieser Stelle

Competitive base salary and incentives

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes andWell

Learning and development opportunities

Zusammenfassung

Icon Clinical Research Hong Kong Limited is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities in Hong Kong. The role emphasizes data integrity, regulatory compliance, and site management across multiple sites.

The candidate will monitor sites, conduct visits, and collaborate with cross-functional teams to ensure timely, accurate data collection. The position requires an advanced degree in life sciences, nursing, or medicine, and travel of up to 60% both

Qualifikationen

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• Extensive experience as a Clinical Research Associate with knowledge of trial processes and regulatory requirements.
• Ability to manage multiple sites and projects with strong organizational and problem-solving skills.

Aufgaben

• Monitor clinical trial sites to ensure adherence to study protocols and GCP standards.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with cross-functional teams to ensure accurate data collection and reporting.
• Provide training and guidance to site staff to maintain high standards.
• Build and maintain relationships with site personnel and stakeholders.

Kenntnisse

GCP knowledge

Data integrity

Site management

Communication skills

Stakeholder management

Travel willingness

Ausbildung

Advanced degree in life sciences / nursing / medicine

Tools

Clinical trial software

Regulatory systems

Jobbeschreibung

Clinical Research Associate II/ Senior Clinical Research Associate

Icon Clinical Research Hong Kong Limited View all jobs

CRA II/ Senior CRA - office-based in Hong Kong. Join us and advance your career with an industry leading CRO.

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
• Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathways