Description
This role offers the opportunity to plan and progress your career as a Senior CRA or CRA with IQVIA, a leading global provider of clinical research services. You will have exposure to wider opportunities like operations management, dedicated customer solutions, project management and more. With dedicated mentoring and structured quarterly reviews, you can build a flexible, meaningful and fulfilling career with no limits.
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
- Collaborating and communicating with a variety of colleagues and customers, with 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