At a Glance
- Tasks: Conduct site visits and ensure compliance in clinical research.
- Company: Join a leading organisation in the health and science sector.
- Benefits: Competitive salary, travel opportunities, and professional growth.
- Other info: Dynamic role with significant travel and remote work options.
- Why this job: Make a difference in healthcare while gaining valuable experience.
- Qualifications: Bachelor's degree in health or science; prior study coordinator experience preferred.
The predicted salary is between 65700 - 80300 $ per year.
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.
Qualifications:
- Bachelor's degree in a health or science related field.
- Prior 1 year of study coordinator experience is preferred.
- Willing to travel approximately 60-80% to locations nationwide is required, or less if remote/virtual visits.
- Strong communication and presentation skills.
- Must be detail-oriented and efficient in time management.
Clinical Research Associate employer: Medpace
Medpace is an exceptional employer, offering a dynamic work environment in Melbourne that fosters professional growth and development within the clinical research field. With a strong focus on employee well-being, competitive compensation, and flexible working arrangements, Medpace supports its team members in achieving their career aspirations while contributing to meaningful advancements in medical therapeutics. Join a globally recognized leader in the CRO industry, where your expertise will be valued and your contributions will make a real impact.
