At a Glance
- Tasks: Assist with clinical documentation and ensure regulatory compliance for trials.
- Company: Join IQVIA Inc., a leader in healthcare data and analytics.
- Benefits: Gain valuable experience in clinical trials and enhance your professional skills.
- Other info: On-site role in North Sydney with opportunities for career advancement.
- Why this job: Be part of groundbreaking research that impacts patient care and health outcomes.
- Qualifications: Strong English communication, MS Office skills, and organisational abilities required.
The predicted salary is between 47250 - 57750 $ per year.
IQVIA Inc. is seeking an Administrative Support specialist to assist CRAs and RSU teams with clinical documentation, TMF maintenance, and regulatory compliance.
You’ll handle filing, archiving, and distribution of trial materials within project timelines.
The role requires strong English communication, MS Office proficiency, and solid organizational skills.
Prior clinical trials experience and knowledge of GCP/ICH are advantageous, with on-site responsibilities in North Sydney.
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Clinical Trials Documentation & Compliance Assistant in North 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.
