Job Overview
Provide project related assistance to assigned project teams.; Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements.; Meeting quality and timeline metrics.

Essential Functions

Complete appropriate role-specific training to perform job duties.;
Under supervision, provides study level administrative support to the clinical study management team (examples of such tasks include, but not limited to running system reports, preparing and distributing status reports, creating and maintaining study trackers, follow-up for outstanding issues, etc.).;
Under supervision, assist in updating and maintaining systems within project timelines/plans and driving tracking compliance in various systems to enable credible data for analysis.;
Perform the activities as per the task list delegated by CMS leads.;
Assist CMs in the preparation of i-site pack for their respective sites and countries for assigned studies, by pulling associated reports.;
Perform assigned access management related administrative tasks to support team members with project execution, example of tasks includes, but not limited to processing access requests, following up with relevant vendors, etc.;
Provide support to technical solution specialist (TSS) on formulations in Excel and on the front-end part.;
Periodic review of site level KRIs and historic site performance according to Central Monitoring Plan
Facilitating early identification of site-level risk/issue(s) occurring during study conduct and responsible for identification of risk
Monitor site performance and make recommendations for timely corrective actions (eg Site Telephone Contact or Triggered Onsite Monitoring Visit)
Review the effectiveness of the recommended actions and take appropriate additional actions if no effect is observed
Review of the Study Central Monitoring Plan
Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested
Adhere to the key activities outlined in the SOW as per customer requirements

Qualifications

B Sc Degree in Life Sciences or educational equivalent.
Fluency in Dutch essential
Requires minumum of 2 years of work experience with minimum 6 months relevant experience.
Basic knowledge of applicable research and regulatory requirements, i.e. International Conference on Harmonisation - Good Clinical Practice and relevant local laws, regulations, and guidelines.
Exposure to Microsoft Applications including but not limited to Microsoft Word, Excel and PowerPoint.
Effective written and verbal communication skills including good command of English language.
Effective time management skills.
Results and detail-oriented approach to work delivery and output.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Strong listening and phone skills.
Good data entry skills.

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.

Associate Centralized Monitor, Dutch Speaking, South Africa