Clinical Trials Coordinator

MSD; Sydney; On-site; AUD 90,000 - 120,000; Full time

Benefits offered by this job

Flexible working arrangements

Competitive remuneration and benefits

Job summary

MSD in Sydney, Macquarie Park, seeks a Clinical Trials Coordinator to support trial and site administration across the clinical trial lifecycle, ensuring site-ready dates and compliant documentation.

You will collaborate with Clinical Operations Manager, CRM and CRA, manage budgets, agreements and payments, maintain eTMF and support regulatory submissions while fostering a flexible, collaborative team environment.

Qualifications

• 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.
• Strong IT skills, including MS Office, Excel and clinical applications.
• Ability to manage multiple tasks in a changing environment.

Responsibilities

• Track essential documents and report safety reports.
• Update CMS and tracking tools; ensure study tools and documents are distributed.
• Support budgeting, contracts, CTRAs, and payments.
• Assist with eTMF reconciliation and quality control activities.
• Prepare Investigator Trial File binders and translations of documents.
• Plan and support investigator meetings and study-related activities.
• Demonstrate digital proficiency with clinical systems and data tools.

Skills

Analytical thinking

Problem solving

Communication skills

Time management

Multitasking

Education

Bachelor’s degree or relevant training

Tools

MS Office

Excel

Clinical applications

Job description

Job Description

Clinical Trials Coordinator (CTC)

• Permanent full-time role with competitive renumeration 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:

Analytical Problem Solving, Clinical Data Management, Clinical Documentation, Clinical Reporting, Clinical Research Administration, Clinical Trial Compliance, Clinical Trial Documentation, Clinical Trial Regulations, Clinical Trial Administration, Clinical Trial Support, Data Analysis, Good Clinical Practice (GCP), Medical Documentation, Recordkeeping, Reporting Tools

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:

09/22/2026

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