MEDPACE Jobs in Australia

Clinical Research Associate Entry · Medpace offers full-time employment and a dynamic working environment with varying responsibilities day-to-day. Employees work within a team of therapeutic and regulatory experts. · Key benefits include: · Defined CRA promotion and growth ladde ...

We are seeking Advanced Clinical Practitioner/Nurse Practitioners with Haematology/Oncology experience who are interested in being at the forefront of new treatments for patients with haematologic and oncologic diseases. · Serve as a key clinical resource for the study team; · Su ...

Site Contract Specialist · A clinical contract research organization is seeking an experienced Site Contract Specialist to join their team in Melbourne. · Negotiate contracts and budgets with sponsors and sites · Collaborate with project teams to ensure successful study execution ...

Responsibilities: · Manage day-to-day operations of the project according to ICH/GCP and applicable laws. · Serve as primary Sponsor contact for operational project-specific issues. · Maintain in-depth knowledge of protocol, therapeutic area, and indication. · ...

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager to join their team in Melbourne. · ...

We are currently seeking a full-time Study Start up Submissions Coordinator to join our Clinical Operations team in the Australia office. · ...

Job Summary · The Associate Clinical Trial Manager will support Project Coordinators and Clinical Trial Managers in project management activities. · Communicate and collaborate on global study activities. · Ensure timely delivery of recurrent tasks consistently with a high degree ...

As a Clinical Site Relationship Coordinator with Medpace, you will be responsible for building and maintaining strong relationships with clinical sites in Melbourne. · Key Responsibilities: · Conduct feasibility studies to identify suitable clinical sites · Support trial manageme ...

Clinical Research Associate Job Description · Overview · Medpace offers flexible working conditions, including remote work options and flexible hours, as well as competitive transportation allowances and opportunities for professional growth. · Responsibilities: · Conduct qualifi ...

We are currently seeking a full-time, office based Entry level Regulatory Submissions (Study Start up) Coordinator to join our Clinical Operations team in the Australia, Melbourne office. · ...

Clinical Research Project Coordinator · The Clinical Research Project Coordinator plays a vital role in our team. · <ol style= ...

Job Summary: · This Experienced Regulatory Submissions Coordinator role plays a vital part in our Clinical Operations team at Medpace. · The ideal candidate will have expertise in preparing and submitting regulatory applications to TGA / Medsafe. · ...

A leading clinical research organization seeks an Associate Clinical Trial Manager to support project coordinators with project management activities in clinical trials. This role offers extensive training and career growth opportunities. · Key Responsibilities · Serving as liais ...

We provide Phase I-IV clinical development services to the biotechnology, · pharmaceutical and medical device industries. · ...

We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. · A full-service clinical contract research organization (CRO). · ...

Key Responsibilities: · Communicate and collaborate on global study activities · Ensure timely delivery of recurrent tasks consistently with high accuracy · Compile and maintain project-specific status reports within the clinical trial management system · The ideal candidate will ...

Join our Clinical Operations team in Melbourne,Australia. We're seeking a Clinical Site Relationship Coordinator who will work pre-award and post-award study feasibilities. · This coordinator will be responsible for: · Serve as site relations partner by providing oversight and bu ...

Clinical Trial Managers with expertise in Oncology related are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. · Manage and provide accountability for day-to-day operations of the project · Serve as primary Sponsor contact for operat ...

Oncology Ctm Associate: Global Study Management Position Overview: · The role involves supporting project coordinators and managers in globally-focused environment emphasizing strong organizational and communication skills. · Candidates will benefit from extensive training, caree ...

Oncology Clinical Trial Manager · We are seeking a Project Manager to oversee day-to-day operations of clinical trials, particularly in oncology. · A minimum 2 years experience in clinical trial management required. · About this role: · ...