Mô tả công việc
Your responsibilities will include:
- Performing site selection, initiation, monitoring, and close‑out visits, plus maintaining appropriate documentation
- Supporting the development of a subject recruitment plan
- Establishing regular lines of communication plus administering protocol and related study training to assigned sites
- Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You will need to have a good knowledge of applicable clinical research regulatory requirements.
Qualifications:
- University degree in scientific discipline or healthcare
- At least 1 year of on‑site monitoring experience
- Good knowledge of GCP and clinical research regulatory requirements
- Good computer skills including MS Office
- Excellent command of English language
- Organizational, time management and problem‑solving skills
- Ability to establish and maintain effective working relationships with colleagues, managers, and customers.
- Flexibility to travel.
What you can expect:
- Working with different customers on global trials
- Career development opportunities for those who are passionate in wanting to grow as part of the organization.
- Leaders that support flexible work schedules/arrangement
- Excellent working environment in a stable, international, reputable company
- Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape
- Attractive remuneration package.
#LI-Hybrid
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.