Description
This role offers you the opportunity to plan and progress your career as a Senior CRA or CRA at IQVIA, a leading global provider of clinical research services. You will have dedicated mentoring and receive structured quarterly reviews on performance, promotion opportunities and awards. 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.