At a Glance
- Tasks: Build and maintain strategic relationships with clinical sites while supporting study feasibilities.
- Company: Join Medpace, a leading clinical research organisation dedicated to innovative drug development.
- Benefits: Competitive pay, health benefits, flexible work options, and ongoing professional development.
- Other info: Dynamic office culture with mentorship and clear career advancement paths.
- Why this job: Make a real impact in clinical research and grow your career in a supportive environment.
- Qualifications: Bachelor's degree and 1-2 years of clinical monitoring experience required.
The predicted salary is between 67500 - 82500 $ per year.
Our clinical activities are growing rapidly, and we are currently seeking a full-time office-based Clinical Site Relationship Coordinator to join our vibrant Clinical Operations team in Melbourne, Australia. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies to effectively conduct feasibilities in Australia. This position will fit someone who has previous clinical research experience or perhaps a CRA who would like to reduce travel.
If you want an exciting career within a company that excels in delivering innovative research and development of cutting edge drugs, where you can grow your potential, then this is the opportunity for you.
Responsibilities
- Serve as site relations and excellence partner by providing oversight and building/retaining relationships of assigned sites within assigned country;
- Support Management in conducting/expediting feasibility activities (standalone, blinded, initial, ongoing), site selection/alignment with studies and/or therapeutic areas, and study start-up;
- Proactively research and understand specified site landscape/intelligence (KOL presence and knowledge, site capabilities, country standard of care and medical practices, etc.) as it relates to specific patient population, recruitment, and retention;
- Building and maintaining relationships with preferred site networks/flagship sites which includes facilitating master CDAs and holding meetings with network directors as needed;
- Provide ongoing support of sites, including identifying and discussing future new business;
- Develop effective plans for site contacts, troubleshooting, and follow-up;
- Serve as main point of contact for project teams regarding site performance issues and updates on pertinent site information;
- May be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc.
Qualifications
- Bachelor's degree and 1-2 years of Clinical Monitoring experience;
- Broad knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines;
- Demonstrated organizational and prioritization skills;
- Demonstrated oral and written communication skills;
- Proficient knowledge of Microsoft Office applications.
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.
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.
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.
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.
Clinical Site Relationships Specialist – Melbourne employer: Medpace
Medpace is an exceptional employer, offering a dynamic work environment in Melbourne that fosters professional growth and development within the clinical research field. With a strong focus on employee well-being, competitive compensation, and flexible working arrangements, Medpace supports its team members in achieving their career aspirations while contributing to meaningful advancements in medical therapeutics. Join a globally recognized leader in the CRO industry, where your expertise will be valued and your contributions will make a real impact.
