Clinical Trials Assistant 2 at IQVIA. - Turkey

Sydney, New South Wales, Australia -

Full Time

Start Date

Immediate

Expiry Date

06 Mar, 26

Salary

0.0

Posted On

06 Dec, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trials, Administrative Support, Communication Skills, Problem-solving Skills, Clinical Documentation, Regulatory Requirements, Good Clinical Practice, International Conference On Harmonization, eTMF, CTMS, Tracking Information, Study Files, Clinical Monitoring, Project Timelines, Team Collaboration, Documentation Management

Industry

Hospitals and Health Care

Description

As a CTA joining our Functional Service Partnerships Team in a client facing role, you will provide administrative support to clinical projects and update clinical systems and databases. Responsibilities: Assisting preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. 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 Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., eTMF and CTMS) that track site compliance and performance within project timelines. 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 and with required approval. Qualifications: Minimum 1 year experience in a CTA role. Experience accurately updating and maintaining clinical documents and systems (e.g., eTMF and CTMS). Exceptional communication, computer, and problem-solving skills. Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. High or Secondary School diploma/certificate or country’s educational equivalent and 3 years administrative support experience; or equivalent combination of education, training, and experience. Benefits: Well-established onboarding and continuous training and development opportunities IQVIA benefits including extra leave and health allowance Being part of a company that promotes and supports a healthy work life balance Strong, stable and experienced team and supportive managers 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 a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

The Clinical Trials Assistant will provide administrative support to clinical projects, including the preparation and distribution of clinical trial supplies and documentation. They will also assist with maintaining clinical systems and act as a central contact for project communications.