27 jobs in IQVIA

This role can be based in Australia or New Zealand and will prioritise candidates not requiring visa sponsorship. This is a 1 year contract role, and renewal or conversion is dependent on business needs.
**Responsibilities**
+ Formulate strategies and action plans to maximize delivery of a high-quality team/department monitoring service, ensuring achievement of individual/team/department targets, aligning with company strategies.
+ Manage, develop, coach, and motivate team members to develop their skills to ensure that a high professional standard is achieved, and project targets are met. Be an advocate for individual career development.
+ Conduct Accompanied Site Visits (ASV's) to develop CRA skills. Support CRA's on solving project specific issues across site portfolio.
+ Identify quality risks and issues and suggest appropriate corrective action plans to appropriate management to prevent or correct deficiencies in performance of employees.
+ Share IQVIA and client key goals and drivers with your team members.
+ Drive decision making in line with these.
+ Attend client meetings, maintain relationships with any local client affiliates.
+ Maximize profitability by ensuring project objectives and customer requirements are achieved.
+ Ensure that staff have the proper materials, systems access and training to complete job responsibilities. Provide oversight for the execution of the training plan and mentored training experiences.
+ Ensure timely and accurate reporting of required information on relevant systems.
+ Support continuous improvement of monitoring processes to deliver quality, consistency and efficiency in delivery.
+ Participate in the selection process for new staff by conducting candidate review and participating in the interviewing process. Conduct on-boarding training for new staff in conjunction with Human Resources and Learning and Development training programs.
Responsibilities include planning, assigning, and directing work; gathering feedback for appraising performance, guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems. Approve actions on human resources matters in consultation with Human Resources and other relevant departments.
**Requirements**
+ Significant experience in clinical trial management in a CRO or Pharmaceutical setting
+ Minimum 2 years experience in a managerial role
+ Strong in resource planning and team coordination.
+ Strong leadership and organizational skills to manage complex projects and team dynamics.
+ Proficiency in clinical documentation, project management tools, and resourcing systems.
+ Excellent communication and interpersonal skills to collaborate effectively across teams and stakeholders.
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 is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

This role can be based in Australia or New Zealand and will prioritise candidates not requiring visa sponsorship. This is a 1 year contract role, and renewal or conversion is dependent on business needs.
**Responsibilities**
+ Formulate strategies and action plans to maximize delivery of a high-quality team/department monitoring service, ensuring achievement of individual/team/department targets, aligning with company strategies.
+ Manage, develop, coach, and motivate team members to develop their skills to ensure that a high professional standard is achieved, and project targets are met. Be an advocate for individual career development.
+ Conduct Accompanied Site Visits (ASV's) to develop CRA skills. Support CRA's on solving project specific issues across site portfolio.
+ Identify quality risks and issues and suggest appropriate corrective action plans to appropriate management to prevent or correct deficiencies in performance of employees.
+ Share IQVIA and client key goals and drivers with your team members.
+ Drive decision making in line with these.
+ Attend client meetings, maintain relationships with any local client affiliates.
+ Maximize profitability by ensuring project objectives and customer requirements are achieved.
+ Ensure that staff have the proper materials, systems access and training to complete job responsibilities. Provide oversight for the execution of the training plan and mentored training experiences.
+ Ensure timely and accurate reporting of required information on relevant systems.
+ Support continuous improvement of monitoring processes to deliver quality, consistency and efficiency in delivery.
+ Participate in the selection process for new staff by conducting candidate review and participating in the interviewing process. Conduct on-boarding training for new staff in conjunction with Human Resources and Learning and Development training programs.
Responsibilities include planning, assigning, and directing work; gathering feedback for appraising performance, guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems. Approve actions on human resources matters in consultation with Human Resources and other relevant departments.
**Requirements**
+ Significant experience in clinical trial management in a CRO or Pharmaceutical setting
+ Minimum 2 years experience in a managerial role
+ Strong in resource planning and team coordination.
+ Strong leadership and organizational skills to manage complex projects and team dynamics.
+ Proficiency in clinical documentation, project management tools, and resourcing systems.
+ Excellent communication and interpersonal skills to collaborate effectively across teams and stakeholders.
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 is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Solution Specialist - Clinical eSource Platform**
**Location:** Sydney or Melbourne
**Experience Required:** 5+ years
We are seeking a **Solution Specialist** to serve as a SaaS implementation and support expert for IQVIA's Clinical eSource Platform. In this role, you will partner with early-phase CROs and Sponsors to drive successful platform adoption, delivering high-quality support, training, and implementation expertise.
This is a client-facing position ideal for someone with strong clinical trial experience, technical aptitude, and a passion for problem-solving in a fast-paced environment.
**Key Responsibilities**
+ Support the implementation and ongoing use of IQVIA's Clinical eSource Platform across early-phase studies
+ Develop deep subject matter expertise across platform capabilities (recruitment, study design, data collection, reporting)
+ Own and manage customer service desk tickets, ensuring timely resolution within SLAs
+ Partner with cross-functional teams (Engineering, Product, Sales, and Project Management) to deliver effective solutions
+ Lead client onboarding activities, including:
+ Delivering product training and instructional workshops
+ Running status meetings and tracking implementation progress
+ Gathering requirements for configuration or enhancements
+ Troubleshooting issues and proposing practical solutions/workarounds
+ Provide ongoing technical support and best practice guidance to clients
+ Participate in audits, demos, and commercial activities (e.g., RFIs) as an eSource SME
+ Contribute to documentation, testing, and validation of new product features
+ Manage multiple priorities in a dynamic, customer-facing environment
+ Travel to client sites as needed for key milestones (e.g., go-live, training)
**Required Skills & Experience**
+ Bachelor's degree in relevant field
+ 5+ years' experience in an early-phase clinical research environment
+ Hands-on experience with eSource, EDC, or eCRF systems
+ Experience using ClinSpark ideal
+ Strong technical aptitude with ability to quickly learn new platforms
+ Proven experience troubleshooting complex technical issues
+ Excellent communication skills, with the ability to explain technical concepts to non-technical users
+ Strong time management and prioritisation skills
+ Ability to work independently and take ownership of deliverables
+ Experience in a client-facing or customer support role
+ Strong collaboration skills across cross-functional teams
+ Experience configuring or designing eSource data collection systems
+ Hands-on study floor experience, including electronic data capture
+ Experience working with clinical stakeholders (physicians, nurses, coordinators, data managers)
+ Training or instructional delivery experience
**Why Join IQVIA?**
At IQVIA, you'll be part of a global leader in clinical research and healthcare technology, working on innovative SaaS solutions that advance clinical trials and improve patient outcomes.
If you are interested please apply with your resume. If you are successful you will receive an email to complete an online assessment.
Candidates who pass this assessment will be contacted direct by the IQVIA Recruiter to discuss.
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 is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

IQVIA is seeking a GP Sales Representative to support one of our pharmaceutical clients in the **Perth WA North territory** . Working as part of an established and high-performing sales team, you will represent a leading diabetes portfolio, engage healthcare professionals, and contribute to improved patient outcomes while driving business growth.
Reporting to the State Sales Manager, your objective is to gain acceptance of our products by key Doctors to achieve desired patient outcomes. You will utilize your excellent targeting and profiling abilities to build strong business-oriented relationships with your customers. Your insights on developing and delivering a comprehensive territory plan will drive value and growth; focusing to achieve sales targets and marketing objectives for designated products while maintaining a high level of product and disease state knowledge.
**Qualifications:**
+ You are ideally tertiary qualified in a Science or Business discipline.
+ A proven track record in sales.
+ Strong Knowledge of the territory.
+ GP Sales experience within the Diabetes space will be highly regarded.
+ Strong B2B sales.
+ Self-assured and persuasive.
+ Quick thinking and an ethical professional who excels working in a targeted environment.
+ Excellent networking skills and strategic focus to drive these.
If you are interested in this role please apply with your CV and a member of the Talent Acquisition team will be in touch.
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 is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Medical Sales Representative - Adelaide North**
**Contract Opportunity | IQVIA Partnered with a Global Pharmaceutical Leader**
IQVIA is partnering with one of our leading pharmaceutical clients to recruit a Medical Sales Representative in Adelaide North. In this role, you will work alongside the client's established sales team, building strong relationships with healthcare professionals and helping drive positive patient outcomes through innovative healthcare solutions.
**About the Role**
As a Medical Sales Representative, you'll be the face of innovative prescription products, building strong relationships with **General Practitioners and Pharmacists** across your territory. Your mission:
+ **Educate and engage** healthcare professionals on our product portfolio.
+ **Drive sales growth** and achieve targets through strategic territory management.
+ **Collaborate** with cross-functional teams to deliver exceptional results.
This is an exciting opportunity to combine your commercial acumen with a genuine passion for healthcare.
**What We're Looking For**
+ Degree qualified in **Life Sciences, Business, or related field** .
+ Proven success in **medical sales** or similar B2B environment.
+ Strong **communication, presentation, and negotiation skills** .
+ Ability to thrive in a **target-driven, dynamic setting** .
+ Commitment to **ethical standards** and patient care.
**Why Join Us?**
+ Work with a **global leader** in pharmaceuticals.
+ Access to **industry-leading training and resources** .
+ Be part of a **supportive, high-performing team** that values growth and innovation.
**Ready to make a difference?**
Apply now and take the next step in your career while helping transform patient care.
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 is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

We are seeking multiple **Senior Site Activation Specialists** to join our ANZ Site Activation team. This is a great opportunity to work across a broad portfolio of sponsors and therapeutic areas, supporting clinical trials from early site identification through to activation and ongoing maintenance.
You will be responsible for end‑to‑end site start‑up activities, working closely with internal study teams, investigative sites, and external stakeholders to ensure timely and compliant site activation.
Applicants must have full work rights for Australia.
As we are hiring multiple headcounts across various models, some positions are 1 Year contract positions. The conversion or renewal is dependent on business needs, and we are unable to guarantee the allocation of contract or permanent roles, depending on sponsor requirements.
The interview process will include an initial video screening and phone screening stage, and you can indicate your preference on the above during the screening.
**What We Offer**
+ Exposure to a wide variety of sponsors, studies, and therapeutic areas
+ A collaborative, supportive team environment
+ Training, tools, and mentoring within a leading global CRO
+ Flexibility in working location across Australia and New Zealand
**Essential Functions**
+ Support site feasibility, site identification, site start‑up, and maintenance activities across multiple studies and sponsors
+ Prepare, review, and track site start‑up documentation in accordance with regulatory, ethics, and sponsor requirements
+ Act as a key point of contact for investigative sites during start‑up and maintenance phases
+ Independently coordinate ethics and informed consent form (ICF) submissions, including local adaptations and ongoing amendments
+ Lead site budget and contract negotiations
+ Maintain accurate site and study information within internal systems and project trackers
+ Communicate status updates, risks, and timelines effectively to internal stakeholders
+ Provide operational guidance and informal mentoring to less experienced team members
+ Operate with a high degree of autonomy across multiple studies and stakeholders
**Required Experience & Qualifications**
+ Minimum **12 months hands‑on experience in clinical trial site start‑up / site activation activities**
+ Experience managing ethics submissions and informed consent documentation requirements
+ Proven experience in site budget and contract negotiations
+ Strong organisational skills with the ability to manage multiple sites and studies in parallel
+ Excellent written and verbal communication skills
+ Bachelor's degree in Life Sciences, Health Sciences, or a related field (or equivalent experience)
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 is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

We are seeking multiple **Senior Site Activation Specialists** to join our ANZ Site Activation team. This is a great opportunity to work across a broad portfolio of sponsors and therapeutic areas, supporting clinical trials from early site identification through to activation and ongoing maintenance.
You will be responsible for end‑to‑end site start‑up activities, working closely with internal study teams, investigative sites, and external stakeholders to ensure timely and compliant site activation.
Applicants must have full work rights for Australia.
As we are hiring multiple headcounts across various models, some positions are 1 Year contract positions. The conversion or renewal is dependent on business needs, and we are unable to guarantee the allocation of contract or permanent roles, depending on sponsor requirements.
The interview process will include an initial video screening and phone screening stage, and you can indicate your preference on the above during the screening.
**What We Offer**
+ Exposure to a wide variety of sponsors, studies, and therapeutic areas
+ A collaborative, supportive team environment
+ Training, tools, and mentoring within a leading global CRO
+ Flexibility in working location across Australia and New Zealand
**Essential Functions**
+ Support site feasibility, site identification, site start‑up, and maintenance activities across multiple studies and sponsors
+ Prepare, review, and track site start‑up documentation in accordance with regulatory, ethics, and sponsor requirements
+ Act as a key point of contact for investigative sites during start‑up and maintenance phases
+ Independently coordinate ethics and informed consent form (ICF) submissions, including local adaptations and ongoing amendments
+ Lead site budget and contract negotiations
+ Maintain accurate site and study information within internal systems and project trackers
+ Communicate status updates, risks, and timelines effectively to internal stakeholders
+ Provide operational guidance and informal mentoring to less experienced team members
+ Operate with a high degree of autonomy across multiple studies and stakeholders
**Required Experience & Qualifications**
+ Minimum **12 months hands‑on experience in clinical trial site start‑up / site activation activities**
+ Experience managing ethics submissions and informed consent documentation requirements
+ Proven experience in site budget and contract negotiations
+ Strong organisational skills with the ability to manage multiple sites and studies in parallel
+ Excellent written and verbal communication skills
+ Bachelor's degree in Life Sciences, Health Sciences, or a related field (or equivalent experience)
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 is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Solution Specialist - Clinical eSource Platform**
**Location:** Sydney or Melbourne
**Experience Required:** 5+ years
We are seeking a **Solution Specialist** to serve as a SaaS implementation and support expert for IQVIA's Clinical eSource Platform. In this role, you will partner with early-phase CROs and Sponsors to drive successful platform adoption, delivering high-quality support, training, and implementation expertise.
This is a client-facing position ideal for someone with strong clinical trial experience, technical aptitude, and a passion for problem-solving in a fast-paced environment.
**Key Responsibilities**
+ Support the implementation and ongoing use of IQVIA's Clinical eSource Platform across early-phase studies
+ Develop deep subject matter expertise across platform capabilities (recruitment, study design, data collection, reporting)
+ Own and manage customer service desk tickets, ensuring timely resolution within SLAs
+ Partner with cross-functional teams (Engineering, Product, Sales, and Project Management) to deliver effective solutions
+ Lead client onboarding activities, including:
+ Delivering product training and instructional workshops
+ Running status meetings and tracking implementation progress
+ Gathering requirements for configuration or enhancements
+ Troubleshooting issues and proposing practical solutions/workarounds
+ Provide ongoing technical support and best practice guidance to clients
+ Participate in audits, demos, and commercial activities (e.g., RFIs) as an eSource SME
+ Contribute to documentation, testing, and validation of new product features
+ Manage multiple priorities in a dynamic, customer-facing environment
+ Travel to client sites as needed for key milestones (e.g., go-live, training)
**Required Skills & Experience**
+ Bachelor's degree in relevant field
+ 5+ years' experience in an early-phase clinical research environment
+ Hands-on experience with eSource, EDC, or eCRF systems
+ Experience using ClinSpark ideal
+ Strong technical aptitude with ability to quickly learn new platforms
+ Proven experience troubleshooting complex technical issues
+ Excellent communication skills, with the ability to explain technical concepts to non-technical users
+ Strong time management and prioritisation skills
+ Ability to work independently and take ownership of deliverables
+ Experience in a client-facing or customer support role
+ Strong collaboration skills across cross-functional teams
+ Experience configuring or designing eSource data collection systems
+ Hands-on study floor experience, including electronic data capture
+ Experience working with clinical stakeholders (physicians, nurses, coordinators, data managers)
+ Training or instructional delivery experience
**Why Join IQVIA?**
At IQVIA, you'll be part of a global leader in clinical research and healthcare technology, working on innovative SaaS solutions that advance clinical trials and improve patient outcomes.
If you are interested please apply with your resume. If you are successful you will receive an email to complete an online assessment.
Candidates who pass this assessment will be contacted direct by the IQVIA Recruiter to discuss.
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 is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Are you ready to lead the charge in transforming healthcare? At IQVIA, we're looking for a passionate and driven Associate Clinical Project Manager to oversee the delivery of cutting-edge clinical trials that bring new therapies to patients faster. This is your chance to make a real difference-while working with global teams, innovative technologies, and world-class clients.
We regret to inform that we can only shortlist and consider candidates not requiring sponsorship to work in Australia.
**What You'll Be Doing**
As a Clinical Project Manager, you'll be the cornerstone of clinical trial execution - managing timelines, budgets, and quality across regional or global studies. You'll collaborate with cross-functional teams, engage directly with clients, and ensure every milestone is met with precision and purpose.
**Key Responsibilities:**
+ Lead the planning, execution, and delivery of clinical trials in line with contracts and regulatory standards (ICH-GCP, local laws)
+ Develop and implement integrated study management plans with core project teams
+ Serve as the primary point of contact for clients, vendors, and internal stakeholders
+ Monitor project performance, manage risks, and drive resolution of issues
+ Ensure financial success through accurate forecasting, budget control, and scope management
+ Mentor and support junior team members, fostering a culture of excellence and collaboration
+ Represent IQVIA in bid defenses and client meetings, showcasing our capabilities and solutions
**What You Bring**
+ **Education:** Bachelor's degree in Life Sciences or related field (required)
+ **Experience: minimum** 5+ years in clinical research, including 2 + year in project management in Australia
+ **Expertise:** Strong understanding of clinical trial operations, regulatory requirements, and therapeutic areas
+ **Skills:**
+ Leadership and team management
+ Strategic thinking and problem-solving
+ Excellent communication and presentation skills
+ Financial acumen and contract management
+ Proficiency in MS Office (Word, Excel, PowerPoint)
**Why Join IQVIA?**
+ Work on impactful projects that improve lives globally
+ Collaborate with brilliant minds across geographies and cultures
+ Access cutting-edge tools and data-driven solutions
+ Grow your career with continuous learning and development opportunities
+ Be part of a company that values innovation, ownership, and client focus
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 is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled