Clinical Research Coordinator - Research - Clinical

Advara HeartCare group; Adelaide; On-site; AUD 85,000 - 110,000; Full time

Job summary

Advara HeartCare Leabrook – Adelaide is seeking a Clinical Research Co-ordinator, for full-time or part-time roles, to advance cardiology trials. Join a dynamic team focused on improving heart health outcomes in a fast-paced environment.

You’ll work with cardiologists and the wider clinical team, conducting visits, managing study documentation, screening and enrolling participants, and administering trial medications, supported by a values-driven culture committed to quality care.

Qualifications

• Bachelor of Nursing or Pharmacy and current AHPRA registration.
• Strong patient management and clinical skills.
• Excellent communication and interpersonal skills, with the ability to work well independently and as part of a team.
• High computer literacy and proficiency with clinical trials software and MS Office.

Responsibilities

• Conducting study visits and assessments in line with protocol requirements.
• Collaborating closely with cardiologists and the broader clinical team to ensure efficient trial delivery while prioritising patient care.
• Maintaining accurate and up-to-date patient and study documentation.
• Screening and enrolling participants in accordance with eligibility criteria and recruitment targets.
• Managing study documentation and supporting study start-up, ongoing coordination, and close-out activities in a timely manner.
• Administer trial medications.

Skills

Patient management

Clinical skills

Communication

Teamwork

MS Office

Clinical trials software

Education

Bachelor of Nursing or Pharmacy

Job description

Advara HeartCare Leabrook – Adelaide- Clinical Research Co-ordinator

• Full-time or Part-time Role available
• Seeking a Pharmacist or Registered Nurse to join the team

Want to improve Australia’s heart health? Our team is our impact and our future. Join something special at Advara HeartCare.

• Shape the future of cardiology research with a dynamic, supportive team.
• Learn and grow alongside leaders in the industry.
• Enjoy a rewarding role with opportunities to make a meaningful impact in a fast-paced exciting environment .

Your Impact, with Us

You’ll Make a Meaningful Impact By

• Conducting study visits and assessments in line with protocol requirements
• Collaborating closely with cardiologists and the broader clinical team to ensure efficient trial delivery while prioritising patient care
• Maintaining accurate and up-to-date patient and study documentation
• Screening and enrolling participants in accordance with eligibility criteria and recruitment targets
• Managing study documentation and supporting study start-up, ongoing coordination, and close-out activities in a timely manner
• Administer trial medications

What You’ll Bring

• A Bachelor of Nursing or Pharmacy and current AHPRA registration
• Strong patient management and clinical skills
• Excellent communication and interpersonal skills, with the ability to work well independently and as part of a team
• High computer literacy and proficiency with clinical trials software and MS Office

Highly Desired

• Cardiology background
• Clinical Trials experience
• Venepuncture
• Good clinical practice ICH-GCP

Why Advara HeartCare

We’re a values-driven organisation where every person matters. Because whatever your role here, you are our impact and you are our future. Join Advara HeartCare and achieve more than you ever thought possible.

At Advara HeartCare, we care, we work together, we advance, and we deliver. When you join us, you’ll discover meaningful work, a welcoming and supportive team culture, and the opportunity to help shape our journey to something that’s even better.

Ready to Shape Our Future While Building Yours?

We are building something important here, something special. If this sounds like something you would like to be a part of,