CRA I at ICON plc

Sydney, New South Wales, Australia -

Full Time

Start Date

Immediate

Expiry Date

15 Jan, 26

Salary

0.0

Posted On

17 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trials, Data Analysis, Regulatory Compliance, Communication, Teamwork, Stakeholder Management, Medical Data Review, Study Documentation, Feasibility Studies, Patient Safety, Flexibility, Travel

Industry

Biotechnology Research

Description

CRA I (Sydney)/ Hybrid (client office attendance required): Great opportunity to step up and progress your career in a well-established FSP partnership ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Associate I to join a long-term FSP partnership with one of the most established pharmaceutical companies in the industry. If not travelling, you will be working out of the client office in Sydney 2-3 days per week. Within this program you will find a culture focused on teamwork and camaraderie; where every member plays an integral part. You will have the opportunity to work on breakthrough technologies in the areas of cardiovascular, oncology, women’s health, and cell & gene therapy. This is a challenging career path that will support your growth and professional development. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data. What you will be doing Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required. Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff. Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements. Your profile University degree in medicine, science, or equivalent Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data Completion of CRA training, experience accompanying CRA visits Excellent written and verbal communication in English Good social skills enabling you to deal with queries in a timely manner Flexibility to attend the sponsor office regularly. Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Didn’t find the role you were looking for? Even if the perfect role isn’t available right now, we’re always excited to connect with talented individuals. Register to our Talent Community to receive updates on roles that align with your career goals.

Responsibilities

As a Clinical Research Associate I, you will oversee and coordinate clinical trials, ensuring compliance with regulations and collecting critical data. You will work independently to manage study activities and maintain documentation while developing relationships with key stakeholders.