Clinical Trials Coordinator

MSD Australia & New Zealand; Sydney; Híbrido; AUD 90.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible working arrangements

Descripción de la vacante

MSD Australia & New Zealand is seeking a Clinical Trials Coordinator based in Macquarie Park, Sydney, to support trial and site administration across the clinical trial lifecycle. You will help deliver site-ready dates, manage documents, coordinate supply, regulatory submissions, budgeting and payments.

The role involves close collaboration with the Clinical Operations Manager, Clinical Research Manager and Clinical Research Associate, and offers flexible working arrangements within a

Formación

• Bachelor’s degree or relevant training in office management, administration, finance or healthcare.
• Fluent in local language(s) and business proficient in English.
• Strong communication skills, both written and verbal, including with sites and investigators.
• Good understanding of Global and Country/Regional Clinical Research Guidelines, ICH-GCP and Good Documentation Practices.
• Strong IT skills, including MS Office, Excel and clinical applications, with the ability to adapt quickly to new systems.
• Effective time management, organisation, interpersonal, conflict management and negotiation skills.

Responsabilidades

• Track essential documents and report safety reports.
• Ensure collation and distribution of study tools and documents.
• Update Clinical Trial Management Systems and tracking tools.
• Support clinical and non-clinical supply management in collaboration with other country roles.
• Manage labelling requirements and coordinate/sign translation change requests, where applicable.
• Support the CRAs to enter site staff into the training portal to ensure training compliance.

Conocimientos

Communication

English fluency

IT skills

Time management

Independent work

Customer focus

Educación

Bachelor’s degree or relevant job training

Herramientas

MS Office

Excel

Clinical applications

Descripción del empleo

• Permanent full-time role with competitive remuneration and benefits
• The ideal candidate will be based Macquarie Park, Sydney, Australia
• Work with a high performing, agile and passionate team
• We support flexible working arrangements

Job Description

• Permanent full-time role with competitive remuneration and benefits
• The ideal candidate will be based Macquarie Park, Sydney, Australia
• Work with a high performing, agile and passionate team
• We support flexible working arrangements

As a Clinical Trials Coordinator (CTC), you will play a key role in supporting trial and site administration across the clinical trial lifecycle. This is a critical role in helping deliver planned site-ready dates, supporting document management, supply coordination, regulatory submissions, budgeting, agreements and payment activities.

Working closely with local stakeholders including Clinical Operations Manager (COM), Clinical Research Manager (CRM) and Clinical Research Associate (CRA).

What You Will Do

Responsibilities include, however not limited to

Trial and Site Administration

• Track essential documents and report safety reports
• Ensure collation and distribution of study tools and documents
• Update Clinical Trial Management Systems and tracking tools
• Support clinical and non-clinical supply management in collaboration with other country roles
• Manage labelling requirements and coordinate/sign translation change requests, where applicable
• Support the CRAs to enter site staff into the training portal to ensure training compliance

Document Management

• Prepare documents and correspondence
• Collate, distribute/ship and archive clinical documents, including electronic Trial Master File (eTMF)
• Assist with eTMF reconciliation and quality control activities
• Update manuals and documents, such as patient diaries and instructions
• Support proper destruction of clinical supplies
• Prepare Investigator Trial File binders
• Obtain translations of documents

Regulatory and Site Start-Up

• Provide to and collect from investigators forms and lists for site evaluation, site start-up and submissions
• Obtain, track and update study insurance certificates
• Support preparation of submission packages for Ethics / Research Governance Office and Regulatory Agencies (RA)
• Support publication of study results for GCTO and RA, where required by local legislation

Budgeting, Agreements and Payments

• Develop, control, update and close out country and site budgets, including split site budgets
• Develop, negotiate, approve and maintain contracts, including CTRAs
• Track and report contract negotiations
• Update and maintain contract templates in cooperation with Legal
• Calculate and execute payments to investigators, vendors and grants
• Ensure adherence to financial and compliance procedures
• Monitor and track adherence and disclosures
• Maintain tracking tools and process FCPA documentation in a timely manner

Meeting Planning and Support

• Organise meetings, including study memos, letters and protocols
• Support local investigator meetings, including invitations, materials, venue management and vendor support as required
• Support project-related activities as required
• Participate in inclusion initiatives and occupational health and safety activities as required

Digital Proficiency

• Uses approved clinical systems, document-management tools, trackers, metrics dashboards and collaboration platforms accurately; maintains data quality in assigned systems; and applies basic automation, analytics and approved AI-enabled tools with guidance to complete assigned work efficiently, consistently and compliantly.

What You Must Have

• Bachelor’s degree or relevant job training in office management, administration, finance or healthcare
• Fluent in local language(s) and business proficient in English
• Strong communication skills, both written and verbal, including with sites and investigators
• Good understanding of Global and Country/Regional Clinical Research Guidelines, ICH-GCP and Good Documentation Practices
• Strong IT skills, including MS Office, Excel and clinical applications, with the ability to adapt quickly to new systems
• Effective time management, organisation, interpersonal, conflict management and negotiation skills
• High accountability and urgency, with the ability to prioritise and manage multiple tasks in a changing environment
• Ability to work independently and in a matrix, multicultural environment
• Strong customer focus and a proactive, solution-oriented mindset

What You Can Expect

• The opportunity to contribute to the successful delivery of clinical trials
• A collaborative team environment working closely with cross-functional stakeholders
• Ongoing support, development and growth in your role

We are proud to be a company that embraces the value of bringing talented and committed people together. The fastest way to breakthrough innovation is when ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive workplace.

Required Skills

• Accountability
• Analytical Problem Solving
• Clinical Data Management
• Clinical IT
• Clinical Trial Compliance
• Clinical Trial Documentation
• Clinical Trial Management
• Clinical Trials Monitoring
• Clinical Trials Operations
• Clinical Trial Support
• Data Analysis
• Drug Regulatory Affairs
• ICH GCP Guidelines
• Regulatory Compliance

Employee Status Regular

Relocation No relocation

VISA Sponsorship No

Travel Requirements No Travel Required

Flexible Work Arrangements Not Applicable

Shift Not Indicated

Valid Driving License No

Hazardous Material(s) N/A

Job Posting End Date 11/28/2026

• A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID R425064