Jobs at IQVIA

Supports Clinical Research Associates and regulatory teams by maintaining Trial Master Files, clinical documentation, study records, supplies, Case Report Forms, queries, and project communications. Reviews files for completeness, assists with document distribution and archiving, and may support site monitoring visits after training. The role requires administrative and clinical research experience, strong organization, communication skills, Microsoft Office proficiency, and basic knowledge of GCP, ICH guidelines, and clinical protocols.

Drive revenue growth through new client acquisition, strategic account expansion, sponsorship and advertising sales, and healthcare education partnerships. Build relationships with pharmaceutical, medical device, consumer healthcare, and healthcare stakeholders; develop account plans; identify market opportunities; commercialize digital and educational offerings; and engage marketing, medical affairs, commercial leaders, and key opinion leaders.

Conduct site monitoring and management for clinical trials, including selection, initiation, monitoring, and close-out visits. Ensure protocol, GCP, ICH, and regulatory compliance; support recruitment, training, documentation, regulatory submissions, CRF completion, data queries, and Trial Master File maintenance. Collaborate with study teams, resolve site issues, prepare monitoring reports, and support financial management where applicable.

Coordinate and deliver omnichannel healthcare marketing and communications projects across Australia and New Zealand. Responsibilities include developing project plans, managing timelines and risks, coordinating clients, vendors, and internal teams, translating requirements into briefs, supporting campaign setup and quality assurance, and overseeing deployment and reporting. The role requires strong organization, stakeholder communication, data management, prioritization, and attention to detail across multiple concurrent projects.

Manage a territory across Canberra and regional NSW to promote a cardiometabolic product. Engage GPs and specialists, build professional relationships, execute territory plans, support GP sales team obtaining key opinion leaders for educational meetings, and achieve sales targets to improve patient outcomes.

The role involves site monitoring, managing study progress, ensuring regulatory compliance, and communicating effectively with sites and project teams.

The Senior Clinical Research Associate will perform site monitoring and management tasks to ensure compliance with study protocols and regulatory guidelines, manage recruitment plans, and collaborate with study team members for project execution.