Teams 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.