Medical Science Research jobs
- IQVIASydney NSW
- We are currently seeking Clinical Trials Assistant (CTA) to join our Functional Service Partnerships team in a client facing role.
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- University of MelbourneAustralia
- Parental leave
- Health insurance
- Employee assistance program
- Salary packaging
- Hold a tertiary qualification in medical, health science, epidemiology or related discipline, with Honours or Masters.
- 11:55 PM; Melbourne time zone.
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- University of the Sunshine CoastBuderim QLD 4556
- Employee assistance program
- UniSC Clinical Trials | Maroochydore, Sunshine Coast (NEW CLINIC).
- Level 5, $82,843 - $93,358 p.a., plus up to 17% employer superannuation.
- The Royal Women's HospitalParkville VIC
- Annual leave
- Salary packaging
- Part time (0.4 FTE), ongoing role.
- The Public Fertility Services offers a wide range of fertility treatments including but not limited to intrauterine…
- SA HealthSouth Australia
- Annual leave
- Employee assistance program
- Salary packaging
- As an important member of our multidisciplinary team, you will work alongside experienced scientists, technical staff and medical professionals to support the…
- Queensland GovernmentSunshine Coast QLD
- A tertiary degree (or equivalent) formal qualification(s) in medical laboratory science or equivalent.
- As the Medical Laboratory Scientist Microbiology, you…
- Orygen, The National Centre of Excellence in Youth...Parkville VIC
- Salary packaging
- Transportation links
- Extensive background in Pharmaceutical, CRO, Biotech, or academic/medical research settings, with hands-on expertise across study start-up, conduct, and close-…
View similar jobs with this employerIQVIASydney NSW- Health insurance
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference…
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Clinical Research Associate II
Often replies in 1 dayPSI CROSydney NSW- Onsite gym
- As a CRA II at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research…
Clinical Research Associate II
Often replies in 1 dayPSI CROSydney NSW- Onsite gym
- As a CRA II at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research…
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference…
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- The Walter and Eliza Hall Institute of Medical...Parkville VIC 3052
- Salary packaging
- BSc with Honours in a field relevant to drug discovery (eg biological sciences, cell biology), or relevant experience.
- NSW HealthCowra NSW
- Annual leave
- Gym membership
- Employee assistance program
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- Employment Type: Permanent Part Time.
- With 24 hours per week, this role offers the opportunity to maintain a fulfilling career in pathology while enjoying…
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View similar jobs with this employerRoyal Melbourne HospitalMelbourne VIC- Annual leave
- Employee assistance program
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- On-site parking
- Work Type: Ongoing - Full-time.
- Identify and characterise enteric viruses using virus culture and molecular techniques.
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- Thermo Fisher ScientificBrisbane QLD
- Travel reimbursement
- Parental leave
- Employee assistance program
- Paid volunteer leave
- Birthday leave
- Bachelor’s degree in life sciences, nursing, or a related field.
- Good oral and written communication skills, with the ability to communicate effectively with…
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- Department of HealthDarwin NT
- Aligned to those in use in a Haematology, Biochemistry or Transfusion sciences laboratory is highly desirable.
- Job type Full-time Duration Ongoing.
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Job Post Details
Clinical Trial Assistant (1 Year Contract) - job post
Job details
Job type
- Full-time
Full job description
North Sydney, Australia | Full time | Hybrid | R1547309
We are currently seeking Clinical Trials Assistant (CTA) to join our Functional Service Partnerships team in a client facing role. As a vital part of our team, CTAs perform daily administrative tasks to support to clinical projects and update clinical systems and databases. Please only apply if you have full unrestricted Australian work rights. Contract renewal/conversion is dependent on business needs, please only apply if you're comfortable.
You will also perform general administrative tasks as needed. You will have excellent communication, computer, and problem-solving skills, and you will be resourceful, analytical, adaptable, and organised. You will be a natural at building rapport with peers and site staff.
- Prepare, handle, distribute, file, and archive clinical documentation and reports as per the scope of work and standard operating procedures
- Review study files periodically for completeness and accuracy
- Support CRAs and RSU with the management of Clinical Trial Supplies and tracking information
- Track and manage CRFs, queries and clinical data flow efficiently and effectively.
- Communicate with the clinical team and provide relevant project information, correspondence and documentation
Qualifications:
- Minimum 6-12 months experience in a CTA role
- Flexible and adaptable to different levels of education, training and experience
- Updated and maintained clinical documents and systems accurately (e.g., eTMF and CTMS)
- Communicated effectively with clients and stakeholders, mastered various computer applications, and resolved complex issues
- Familiar with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and ensured compliance in all clinical trials
- Completed High or Secondary School diploma/certificate
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
IQVIA 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.
Where you'll work
Hybrid
You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.
Culture
Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.