Internship Clinical Trial Coordinator

Job Description

Internship Clinical Trial Coordinator

• Full-time role with competitive remuneration and benefits

• Location:  Macquarie Park, NSW, Australia (Sydney office-based position)

• Career growth: Expand your expertise in a growing, successful industry

• Professional development: Gain valuable experience in a dynamic, evolving role

What You Will Do

Responsibilities include, however not limited to:

Trial and site administration and management

• Track essential documents and reports (e.g. safety reports)

• Ensure the collation and distribution of study tools and documents

• Update clinical trial databases Clinical Trial Management System (CTMS) and trackers

• Manage clinical and non-clinical supplies in collaboration with other country roles

Document and data management

• Prepare documents and correspondence

• Collate, distribute, ship and archive clinical documents, including electronic Trial Master File (eTMF) documentation

• Assist with eTMF reconciliation

• Prepare Investigator Trial File binders

Regulatory and site start-up responsibilities

Collaborate with other country roles to:

• Provide to and collect from investigators the forms and lists required for clinical studies in a timely manner

• Obtain, track and update study insurance certificates

Budgeting, agreements and payments

Collaborate with finance and budgeting representatives to:

• Calculate and process payments to investigators, vendors and for grants

• Ensure adherence to financial and compliance procedures

• Monitor and track adherence and disclosures

• Maintain tracking tools

• Obtain and process compliance documentation for investigators, sites, institutions in a timely manner

Meeting attendance and planning

• Organise meetings, including creating and tracking study memos, letters and protocols

• Support local GCTO meetings, investigator meetings, including invitations, preparation of materials, venue selection and vendor support where applicable

What You Must have

Qualification & Experience:

• Completed job training in office management, administration, finance, life sciences, engineering, project management or health care is preferred

• And/or a Bachelor’s degree

• Strong communication and interpersonal skills

• Strong attention to detail and good analytical skills

• Proficiency in MS Office, including MS Excel, MS Word and MS PowerPoint

What You Can Expect

• The opportunity to gain practical experience in clinical trial coordination

• Support to develop your skills while working autonomously as part of a collaborative team

• Exposure to a broad range of clinical trial administration, document management and site support activities

• Valuable insight into the operations of a global pharmaceutical organisation

• The chance to build experience, confidence and transferable skills that may support your future career progression

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.

#LI-DNI

Required Skills:

Clinical Trial Compliance, Clinical Trial Documentation, Clinical Trials, Communication, Database Management, Data Entry, Document Management, Email Management, Life Science, Microsoft Excel, Planning, Project Coordination, Regulatory Compliance, Researching

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

05/28/2026

*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.