Auckland Medical Research jobs in Cheltenham, Auckland
- ICON PlcAuckland City, Auckland
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- You will contribute to clinical trial monitoring activities,…
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- North Island - AucklandAuckland City, Auckland
- Employment Type: Permanent Full-Time.
- Protected learning time with dedicated clinical supervision.
- Diverse rotations and broad specialty exposure.
- North Island - Auckland Central AucklandAuckland City, Auckland
- Provide medical support as an investigator to investigator/principal investigator(s) for assigned clinical trials within the Liver Research Unit, as needed.
- IQVIAAuckland City, Auckland
- Auckland, New Zealand | Full time | Hybrid | R1481375.
- Engage in Site Visits: From selection to close-out, your visits will be pivotal in ensuring the success…
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- North Island - Auckland Central AucklandAuckland City, Auckland
- A strong interest in research and clinical trials.
- Gain valuable research and clinical trial experience in Medical Oncology.
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- Auckland University of TechnologyAuckland City, Auckland
- Our staff drive innovative progress through our intensive, productive world-class research and engaging, relevant and practical teaching.
- Auckland University of TechnologyAuckland City, Auckland
- Our staff drive innovative progress through our intensive, productive world-class research and engaging, relevant and practical teaching.
- Acuity InsightsAuckland City, Auckland
- Pay may include activities outside of rating, like job training and participating in research studies.
- Complete virtual, scientifically backed, onboarding…
Haematology Research Fellow
Often replies in 3 daysNorth Shore HospitalNorth Shore, Auckland- Responding to clinical queries from research nurses, study coordinators, patients, clinical research associates and medical monitors.
- Thermo Fisher ScientificAuckland City, Auckland
- Demonstrated understanding of medical/therapeutic area knowledge and medical terminology.
- Effective oral and written communication skills, with the ability to…
- University of AucklandAuckland City, Auckland
- Coordinate research centre operations by providing proactive and organisational support to the Centre Director, including coordinating meetings, managing…
- IQVIAAuckland City, Auckland
- You will utilize your excellent targeting and profiling abilities to build strong business-oriented relationships with your customers.
- North Island - Auckland Central AucklandAuckland City, Auckland
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- IQVIAAuckland City, Auckland
- Auckland, New Zealand | Full time | Hybrid | R1570220.
- The Clinical Functional Service Partnerships (CFSP) Project Team are responsible for the management of…
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- Siemens HealthineersAuckland City, Auckland
- Engage with the broader research community.
- Experience in leading scientific projects in both research and clinical environments from idea creation to study…
- North Island - Auckland Central AucklandAuckland City, Auckland
- Engage in research, quality improvement, and collaboration across clinical and basic science.
- Enjoy visa support and relocation assistance to make your move…
Clinical Research Associate
Job details
Full job description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a CRA II/Sr. at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
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Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
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Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
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Collaborating with investigators and site staff to facilitate smooth study conduct.
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Performing data review and resolution of queries to maintain high-quality clinical data.
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Contributing to the preparation and review of study documentation, including protocols and clinical study reports
Your Profile:
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
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Bachelor's degree in a scientific or healthcare-related field.
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Minimum of 2 years of experience as a Clinical Research Associate.
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In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
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Strong organizational and communication skills, with attention to detail.
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Ability to work independently and collaboratively in a fast-paced environment.
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Willingness to travel as required (approximately 60%)
#LI-DP1
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request .
Are you a current ICON Employee?