IQVIA AG seeks a Senior Clinical Research Associate for a hybrid role in Switzerland. The position focuses on managing global clinical trials, ensuring site compliance, and supporting recruitment efforts within a stable international environment.
This position places the candidate within a well-established, global organization to manage clinical trial activities across various customer projects. The role is designed for professionals who thrive in an international setting and are responsible for overseeing the end-to-end monitoring process of clinical sites.
Responsibilities
- Conduct site selection, initiation, routine monitoring, and close-out visits while ensuring all documentation is accurate and complete.
- Assist in creating and refining plans to improve subject recruitment rates at assigned sites.
- Maintain consistent communication channels with sites and deliver necessary protocol training and study-related education.
- Assess the quality and integrity of site operations, identifying and escalating any compliance or quality issues as needed.
- Track key performance indicators including regulatory submission status, recruitment progress, Case Report Form (CRF) completion, and the resolution of data queries.
Requirements
- Hold a university degree in a scientific field or healthcare discipline.
- Possess a minimum of one year of experience in on-site clinical monitoring.
- Demonstrate strong understanding of Good Clinical Practice (GCP) and relevant clinical research regulations.
- Be proficient in MS Office applications and general computer usage.
- Have excellent command of the English language for written and verbal communication.
- Showcase strong organizational abilities, time management skills, and problem-solving capabilities.
- Build and sustain productive working relationships with internal teams, management, and external clients.
- Be willing and able to travel as required for site visits.
What the company offers
- Access to career development paths for individuals eager to grow within the organization.
- Supportive leadership that accommodates flexible work schedules and arrangements.
- Training programs designed to enhance technical expertise, therapeutic knowledge, and regulatory updates.
- A competitive remuneration package.
About the company
IQVIA AG operates as a stable, international, and reputable entity in the clinical research sector. The company provides a professional environment where employees can contribute to global trials while benefiting from a supportive and structured organizational culture.
- The organization is recognized for its stability and international reach.
- Leadership supports flexible working arrangements to help employees balance professional and personal needs.
- Continuous learning is encouraged through regular training on regulatory changes and therapeutic areas.
Quelle: öffentlich zugängliche Karriereseite des Arbeitgebers. Batchly ist nicht der Arbeitgeber und steht nicht notwendigerweise in einem Vertragsverhältnis mit dem Unternehmen.