At a Glance
- Tasks: Support clinical trial sites and ensure compliance with study protocols.
- Company: Join ICON Strategic Solutions, the world's largest FSP organisation.
- Benefits: Competitive salary, health coverage, and career development opportunities.
- Other info: Collaborative environment with training initiatives and travel opportunities.
- Why this job: Make a real impact on patient treatments while growing your career.
- Qualifications: Bachelor's degree in life sciences or related field; clinical research experience preferred.
The predicted salary is between 64845 - 79255 $ per year.
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 SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency.
What You Will Do:
- Deliver clinical research work to a high standard, working closely with your team and stakeholders.
- Assist in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
- Support site management activities, including documentation preparation, data entry, and tracking site performance metrics.
- Collaborate with cross-functional teams to facilitate communication and address site-related issues effectively.
- Maintain accurate records of site activities and contribute to the preparation of monitoring reports.
- Participate in training and development initiatives to enhance knowledge and skills in clinical trial management.
Your Profile:
You will bring relevant clinical research experience, along with the following qualifications and skills.
- Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.
- Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory.
- Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively.
- Basic knowledge of clinical trial processes and regulatory requirements is a plus.
- Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment.
- Willingness to travel as required (approximately 25%).
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 request.
CTC in Sydney employer: ICON Clinical Research
At ICON Strategic Solutions, we pride ourselves on being an exceptional employer, offering a supportive and collaborative work environment for Clinical Research Associates in Perth, Australia. With a strong focus on employee well-being, we provide competitive benefits, including flexible leave options, comprehensive health insurance, and a commitment to professional development, ensuring that our team members thrive both personally and professionally while contributing to groundbreaking medical advancements.