In-Demand Clinical trial coordinator Jobs in Melbourne Vic

Associate Clinical Trial Manager - PhD / Post-Doc (Oncology)
Medpace, Inc. —South Yarra VIC
- Full-time
- Microsoft Excel
- Management
- Doctoral degree
- Health insurance
- Annual leave
Research Officer
Austin Health —Heidelberg VIC
- Part-time
- Doctoral degree
- Master's degree
- Bachelor's degree
- Health insurance
8d
Research Officer
Victorian Government —Melbourne Northern Suburbs VIC
- Part-time
- Doctoral degree
- Master's degree
- Bachelor's degree
- Health insurance
8d
Project Associate / Snr Project Associate
Avance Clinical —Melbourne VIC
- Full-time
- Nursing
- Analysis skills
- Bachelor's degree
Quick Apply
Administration Coordinator - Radiation Oncology (ONJ)
Austin Health —Heidelberg VIC
- Full-time
- Management
- Customer service
- Administrative experience
- Health insurance
5d
Senior Clinical Research Associate - FSP Melbourne / Sydney
Fortrea —Melbourne VIC
- Full-time
- Management
- Patient monitoring
- Administrative experience
Consultant Haematologist
Monash Health —Clayton VIC
- Part-time
- Medicine
- Doctoral degree
- Clinic
17h
Occupational Therapist – Subcontractor Role
The Care Team Network —West Melbourne VIC
- $90 - $120 an hour
- Contract
- Hybrid work
- Bachelor's degree
- First Aid Certification
- Professional development assistance
- Referral program
Quick Apply
14d

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Associate Clinical Trial Manager - PhD / Post-Doc (Oncology)

Medpace, Inc. -
South Yarra VIC

Apply Now

Job Details

Full-time | Contract

Benefits

Health insurance
Annual leave
Opportunities for advancement

Qualifications

Microsoft Excel
Management
Doctoral degree
English
Research
Administrative experience
Analysis skills
Clinical trials
Communication skills

Full Job Description

Job Summary :

Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Melbourne, Australia office. The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities :

Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager;
Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
Compile and maintain project-specific status reports within the clinical trial management system;
Interact with the internal project team, Sponsor, study sites, and third-party vendors;
Provide oversight and quality control of our internal regulatory filing system;
Provide oversight and management of study supplies;
Create and maintain project timelines; and
Coordinate project meetings and produce quality minutes.

Qualifications :

PhD in Life Sciences;
Experienced in Oncology;
Fluency in English with solid presentation skills;
Ability to work in a fast-paced dynamic industry within an international team;
Prior experience within the CRO or pharmaceutical industry not required but will be advantageous; and
Excellent computer (word-processing, databases, Excel, Windows), organisational, and communication skills.

Medpace Overview :

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace? :

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Apply Now

Refine Your Search

clinical trial coordinator jobs in melbourne vic

Associate Clinical Trial Manager - PhD / Post-Doc (Oncology)

Research Officer

Research Officer

Project Associate / Snr Project Associate

Administration Coordinator - Radiation Oncology (ONJ)

Senior Clinical Research Associate - FSP Melbourne / Sydney

Consultant Haematologist

Occupational Therapist – Subcontractor Role

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