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Senior/principal Clinical Research Associate (Joining Bonus Of Up To $15,000 Aud Or More). Positions Available In Melbourne, Sydney, Brisbane, Adelaide Or Perth.

Medpace - Melbourne, VIC

Health, Medical & Pharmaceutical
Source: uWorkin


Medpace is a global, full-service Clinical Research Organization (CRO) and we are currently hiring individuals for exciting careers in the clinical research field!

What can Medpace offer you?

  • Flexible working conditions – Opportunity to work from home and flexible working hours
  • Joining bonuses of up to $15,000 AUD or more may be available for qualified candidates (5+ years of CRA experience) who join the team
  • Visa sponsorship & transfer for qualified candidates already based in Australia
  • Competitive transportation allowance
  • Annual Merit increases
  • Variable Compensation Bonus Plan – lucrative bonus calculated directly from the number of visits you do
  • Fast PACE®: Accelerated, tailored training program training program based on your experience
  • No metric for minimum required days on site per month.
  • Opportunity for cross-functional and CRA leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager
  • Airline club allowance
  • Casual Dress Code

Why Medpace?

Medpace is a leading, scientifically-driven, full service global CRO providing Phase 1-IV core development services for drug, biologic and device programs. Medpace employs nearly 3,500 people across office locations that span six continents and is growing rapidly, particularly in the Asia Pacific region. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities. Our work is meaningful and our employees thrive in an environment with an important purpose.

  • Provide hope for those living with debilitating diseases
  • Join one of the global leaders in life-saving drug development and device
  • Become part of a community dedicated to changing lives


  • Forbes 2021 America’s Best mid-size companies
  • Fortune’s 100 Fastest Growing Companies 2020
  • Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
  • Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

CRA Responsibilities

  • Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
  • Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
  • Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
  • Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
  • Verification that the investigator is enrolling only eligible subjects;
  • Regulatory document review;
  • Investigational product/drug accountability and inventory;
  • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
  • Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement;
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.


  • Bachelor's degree in a health or science related field and with at least 5+ years of experience in clinical monitoring;
  • Knowledgeable about Clinical Monitoring practices and procedures to represent the function in internal and external (e.g., business development) meetings.

Begin Your Future With Medpace Today! Click apply and contact our recruitment team. 

EO/AA Employer M/F/Disability/Vets

*WARNING: Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money. These scammers pose as legitimate employees from actual companies. Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process.

Melbourne, VIC

Health, Medical & Pharmaceutical


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