We’re searching for a knowledgeable, team-oriented Senior CRA to manage the clinical aspects of full-service global projects in Taiwan. As a Senior CRA at PSI, you will work on the frontline of communication with project stakeholders, ensuring the successful conduct of clinical trials in a variety of therapeutic indications. You will maintain the highest quality standards in the industry, while performing and supervising study start-up, clinical monitoring and site management activities on the country/regional level.
Location: Taipei, Taiwan
- Training, mentoring and supervising study level responsibilities for Junior CRAs
- Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits
- Delivering training of investigators, site staff and project teams
- Work with complex studies
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be involved in site identification process
- Contact for clinical investigators, vendors and support services in regard to study progress
- Participate in feasibility research
- Preparation and delivering of presentations at Investigator’s Meetings
- Preparation for and attendance at company’s audits; resolution of audit findings
- Support to Regulatory Affairs in procurement of site regulatory documents
- Maintenance of study-specific automated tracking systems