Job Description
Location: Sydney/Melbourne other locations can be considered on application,
Work Arrangement: Hybrid (traveling is required and must be flexible to travel to client office)
IQVIA is at the forefront of clinical research, driving innovation and transforming lives. Join our passionate team and be part of groundbreaking studies that shape the future of medicine!
As a Clinical Research Project Manager, you'll be the driving force behind the successful delivery of clinical trials. From initiation to closeout, you'll ensure quality deliverables, coordinate dynamic project teams, and be the primary point of contact with the project sponsor. Your role will be pivotal in advancing medical science and improving patient outcomes.
Responsibilities:
Site Selection: Dive into site feasibility and qualification visits, ensuring top-notch conduct and follow-up.
Collaboration: Partner with central study teams and local stakeholders to select the best sites for our trials.
Recruitment: Lead local teams to meet recruitment targets with high-quality data, all within budget.
Compliance: Keep our trials on track by maintaining management systems and initiating corrective actions.
Vendor Management: Manage vendor services, review invoices, and handle local study supplies with finesse.
Monitoring: Conduct engaging meetings, facilitate training, and ensure exceptional study monitoring standards.
Patient Safety: Prepare informed consent forms and ensure timely reporting of adverse events.
Inspection Readiness: Maintain accurate data and essential documents, ensuring we're always inspection-ready.
Requirements:
Degree in a health or science-related field.
Hematology and oncology experience highly desirable
At least 2 years of local clinical trial project management experience.
Strong knowledge of ICH-GCP, SOPs, local laws, and regulations.
Proficient IT skills and willingness to travel.
Excellent communication skills in English and the country language.
Interview Process: Get ready to showcase your skills in a video recording interview as part of our exciting selection process.
What We Offer:
Competitive salary and benefits package.
Opportunities for professional growth and development.
A collaborative and supportive work environment.
The chance to make a meaningful impact on the advancement of healthcare.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
Work Arrangement: Hybrid (traveling is required and must be flexible to travel to client office)
IQVIA is at the forefront of clinical research, driving innovation and transforming lives. Join our passionate team and be part of groundbreaking studies that shape the future of medicine!
As a Clinical Research Project Manager, you'll be the driving force behind the successful delivery of clinical trials. From initiation to closeout, you'll ensure quality deliverables, coordinate dynamic project teams, and be the primary point of contact with the project sponsor. Your role will be pivotal in advancing medical science and improving patient outcomes.
Responsibilities:
Site Selection: Dive into site feasibility and qualification visits, ensuring top-notch conduct and follow-up.
Collaboration: Partner with central study teams and local stakeholders to select the best sites for our trials.
Recruitment: Lead local teams to meet recruitment targets with high-quality data, all within budget.
Compliance: Keep our trials on track by maintaining management systems and initiating corrective actions.
Vendor Management: Manage vendor services, review invoices, and handle local study supplies with finesse.
Monitoring: Conduct engaging meetings, facilitate training, and ensure exceptional study monitoring standards.
Patient Safety: Prepare informed consent forms and ensure timely reporting of adverse events.
Inspection Readiness: Maintain accurate data and essential documents, ensuring we're always inspection-ready.
Requirements:
Degree in a health or science-related field.
Hematology and oncology experience highly desirable
At least 2 years of local clinical trial project management experience.
Strong knowledge of ICH-GCP, SOPs, local laws, and regulations.
Proficient IT skills and willingness to travel.
Excellent communication skills in English and the country language.
Interview Process: Get ready to showcase your skills in a video recording interview as part of our exciting selection process.
What We Offer:
Competitive salary and benefits package.
Opportunities for professional growth and development.
A collaborative and supportive work environment.
The chance to make a meaningful impact on the advancement of healthcare.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
💡 Quick Summary
Seeking a career-building opportunity? The (Associate) Clinical Project Manager position is now open for candidates interested in the Health Jobs sector. This role in Melbourne offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Health Jobs is a plus.