Clinical Research Associate 3

ICON Clinical Research; Sydney; Presencial; AUD 120.000 - 150.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Retirement plans

Learning and development opportunities

Travel opportunities

Descripción de la vacante

ICON Strategic Solutions is seeking a Senior CRA in Sydney to oversee clinical trial activities ensuring adherence to protocol, regulatory requirements, and industry standards.

You will lead monitoring tasks with a focus on quality and continuous improvement, conducting site visits, and collaborating with cross-functional teams for timely data collection and reporting. International travel up to 60% may be required.

Formación

• Experience in monitoring clinical trials and data integrity.
• Strong understanding of regulatory requirements and GCP.
• Ability to manage multiple sites and projects concurrently.
• Excellent communication and cross-functional collaboration skills.
• Willingness to travel approximately 60% of the time.

Responsabilidades

• Monitor clinical trial sites to ensure adherence to study protocols and GCP.
• Conduct site visits, identify issues, and provide guidance for trial execution.
• Collaborate with cross-functional teams to ensure timely data collection and reporting.
• Provide training to site staff to maintain high standards of conduct.
• Build and maintain relationships with site personnel and stakeholders.

Conocimientos

Clinical trial monitoring

Site management

GCP compliance

Stakeholder management

Educación

Bachelor's degree in a relevant scientific discipline

Herramientas

Clinical trial software

Descripción del empleo

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Key responsibilities include:

• 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:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.

Required qualifications and experience:

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• 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.
• Willingness to travel as required (approximately 60%)

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 resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.