Clinical Research Associate（Fsp Model） Jobs

BA/BS or equivalent or any relevant and qualifying training with a minimum of 5 years of relevant clinical trial management experience.

Global Clinical Trial Management experience.

Knowledge of CFR and GCP/ICH requirements

Support Clinical Trial Manager(s). Collaborates with internal team members, Contract Research Organizations, vendors and sites.

Perform all duties and responsibilities in accordance with CFR, GCP/ICH Guidelines, SOPs, and other applicable guidelines.

Excellent leadership, communication, and organizational skills. Able to multi-task under limited direction and on own initiative.

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.

Excellent time management and social skills

Minimum of 2 years of active independent field monitoring experience - all types of visits.

Strong interpersonal, written, and verbal communication skills within a matrixed team.

Experience working in a self-driven capacity, with a sense of urgency and limited oversight.

Benefits Of Working With Parexel FSP

EBS/BA/MS/Ph.D. in Life Sciences with 2+ yrs relevant clinical research experience

Pharmaceutical and clinical drug development experience in a Clinical Scientist role

Proven ability to effectively manage multiple complex studies

2 years of Medical Monitoring experience required

Aggregate Data Review experience required

Excellent Excel and PP skills required

Pre-Study/Start up Site Management Activities

Verify storage and shipment of biological samples and other protocol specific diagnostics requirement

At least 3-5 years clinical operation monitor experience for senior position.

Good knowledge in GCP for senior position

Good communication and organization skills

Identify potential sites, investigators and site staff;