Senior Clinical Study Coordinator

Proclinical Staffing; Sydney; On-site; AUD 95,000 - 115,000; Full time

Job summary

Proclinical Staffing in Sydney is seeking a Senior Clinical Study Coordinator to join their Clinical Operations team. The role involves managing multiple clinical trial activities from start-up to close-out and supporting early phase oncology and haematology studies.

You will mentor junior staff, leverage your nursing or science background, and apply ICH-GCP knowledge. The position is full-time onsite with a salary range around A$95,000 to A$115,000 per year plus bonus and super.

Qualifications

• Tertiary qualification in health, social and/or biological science.
• 2–3 years experience as a clinical study coordinator or similar.
• Nursing background and Oncology experience is preferred.
• Excellent organisation, time management, and problem solving skills.
• Strong knowledge of clinical research and ICH GCP.

Responsibilities

• Manage multiple clinical trial activities from start-up to close-out.
• Mentor and train junior team members.

Skills

Clinical trial coordination

Project management

Excellent communication

Education

Tertiary qualification in health, social and/or biological sciences

Tools

ICH-GCP knowledge

Job description

1 week ago Be among the first 25 applicants

This range is provided by Proclinical Staffing. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

A$95,000.00/yr - A$115,000.00/yr

Senior Consultant - Clinical Operations - Proclinical

Proclinical has an exciting opportunity to join a rapidly growing and reputable Clinical Research Facility, they work across a broad range of different therapeutic areas and also have a large focus in early phase Oncology and Haematology clinical studies. They are growing significantly at present and will offer excellent development and progression opportunities.

They are looking for a dedicated and passionate Senior Clinical Study Coordinator to join their team. You will be responsible for managing multiple clinical trial activities from start up to close out. The role will also involve taking on mentoring and training responsibilities for the junior team members.

Key Requirements

• Tertiary qualification in health, social and/or biological science.
• Ideally 2-3 years experience as a clinical study coordinator, or similar role, preferably working with clinical trial patients in early phase clinical trials.
• Nursing background and Oncology experience is preferred.
• Excellent organisation, time management, and problem solving skills.
• Strong knowledge of clinical research, ICH GCP.

This is a full time and permanent position based onsite in Sydney. They are offering a competitive salary around $95-$115K (depending on experience) + bonus + Super.

Please click APPLY or if you have any questions, please contact Shannon by email - [e-mail]

Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Health Care Provider, Project Management, and Research

Industries

Hospitals and Health Care, Biotechnology Research, and Research Services