Internship Clinical Trial Coordinator at MSD
MPN2, , Australia -
Full Time


Start Date

Immediate

Expiry Date

12 Nov, 25

Salary

0.0

Posted On

12 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Finance, Event Planning, Information Systems, Vendor Management, Document Management, Order Management, Email Management, Supply Management, Travel Coordination, Life Science, Life Sciences

Industry

Pharmaceuticals

Description

Job Description

INTERNSHIP CLINICAL TRIAL COORDINATOR

  • Permanent full-time role with competitive remuneration and benefits
  • Location: Sydney, Australia, Macquarie Park
  • Career growth: Expand your expertise in a growing, successful industry
  • Professional development: Gain valuable experience in a dynamic, evolving role
  • Environment: Work with a supportive, collaborative team
  • To be successful in this role: your knowledge, passion, and enthusiasm on clinical research and trial is key
    We are looking for a full time Intern to support our company’s Global Clinical Trial team in performing selected routine activities that will result in good internal customer outcome.
    You will be coached, and mentored by our qualified, experienced, and professional clinical trial team in Australia and New Zealand

QUALIFICATION & EXPERIENCE:

  • Completed job training (office management, administration, finance, life sciences, engineering, project management, health care preferred) and/or Bachelor’s Degree

REQUIRED SKILLS:

Clinical Information Systems, Database Management, Data Entry, Document Management, Email Management, Event Planning, Life Science, Management Process, Office Management, Payment Handling, Purchase Order Management, Researching, SAP Systems, Supply Management, Travel Coordination, Vendor Management

How To Apply:

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Responsibilities

REGULATORY & SITE START-UP RESPONSIBILITIES:

Collaborate with other country roles to:

  • In a timely manner, provide to and collect from investigators forms/lists for site
  • evaluation/validation, site start-up and submissions
  • Obtain, track and update study insurance certificates
  • Support preparation of submission package for IRB/ERC and support regulatory agencies
  • submissions.
  • Publish study results for GCTO and RA where required per local legislation
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