At a Glance
- Tasks: Support clinical teams by managing documents and ensuring compliance in exciting research projects.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Gain valuable experience, develop skills, and contribute to innovative medical treatments.
- Other info: Opportunity for growth and learning in the fast-paced world of clinical research.
- Why this job: Make a real difference in patient outcomes while working in a dynamic environment.
- Qualifications: High school diploma and 2 years of admin support in clinical trials required.
The predicted salary is between 41850 - 51150 $ per year.
Essential Functions
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e. g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
Qualifications
- High School Diploma or equivalent
- Min 2 years administrative support experience in clinical trials.
- Equivalent combination of education, training and experience.
- Computer skills including working knowledge of Microsoft Word, Excel and Power Point.
- Written and verbal communication skills including good command of English language.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Awareness of applicable clinical research regulatory requirements, i. e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
- Knowledge of applicable protocol requirements as provided in company training.
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.
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Clinical Trials Assistant in Sydney employer: IQVIA Inc
IQVIA Inc offers a dynamic work environment where healthcare professionals can engage in meaningful clinical research and patient care. The company provides extensive training and ongoing education, ensuring that employees are well-prepared to deliver high-quality, patient-centred services. Opportunities for professional growth and the chance to work autonomously in diverse settings make IQVIA an attractive employer for registered nurses and clinical research professionals.
