Pathology Clinical Trials and Research Manager at Monash Health
Clayton VIC 3168, Victoria, Australia -
Full Time


Start Date

Immediate

Expiry Date

26 May, 25

Salary

0.0

Posted On

26 Mar, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

NOW RECRUITING A PATHOLOGY CLINICAL TRIALS & RESEARCH MANAGER - FULL TIME FIXED TERM UNTIL 15 NOVEMBER 2026

Are you an experienced professional with a passion for clinical trials and research? We are seeking a highly motivated individual to oversee all aspects of Clinical Trials within Pathology.

Responsibilities

ABOUT THE ROLE

As the Clinical Trials and Research Lead, you will play a pivotal role in managing the planning, coordination, and oversight of all clinical trials within Pathology. You will ensure compliance with regulatory requirements, oversee financial management, and develop standard operating procedures to support research excellence. Strong stakeholder engagement is critical, as you will work closely with internal and external partners to drive high-quality clinical trials and research outcomes.

KEY RESPONSIBILITIES:

  • Oversee all clinical trials activity within Pathology, ensuring seamless coordination and execution.
  • Develop and maintain relationships with key stakeholders, including researchers, clinicians, pharmaceutical companies, and regulatory bodies.
  • Manage financial aspects of clinical trials, including budgeting, financial reporting, and contract negotiations.
  • Prepare tenders for major research projects and develop financial agreements for approval.
  • Implement and maintain standard operating procedures for all clinical trials processes.
  • Ensure compliance with ethics submissions, regulatory requirements, and safety reporting protocols.
  • Participate in and conduct internal and external audits to uphold research integrity.
  • Maintain and manage the Clinical Trials Database.

TO SUCCEED IN THIS ROLE, YOU WILL HAVE:

  • Experience in clinical trials management, research administration, or a related field.
  • Strong knowledge of ethics submissions, regulatory affairs, and financial reporting in research settings.
  • Excellent stakeholder engagement skills, with the ability to build relationships across clinical, academic, and industry sectors.
  • High attention to detail, problem-solving skills, and the ability to manage multiple projects effectively.
Loading...