Parexel
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+
💰 Venture Round on 1990-01
Senior Clinical Research Associate - FSP
September 15
Parexel
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+
💰 Venture Round on 1990-01
Description
• You will be dedicated to a single client. • You will be responsible for all site management and supervisory activities in the assigned oncology studies. • You will work with industry leaders and subject matter experts. • You will have the opportunity to mentor junior CRAs. • You will work with world-class technology. • You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.
Requirements
• Extensive experience in site management, with knowledge of clinical trial methodology and terminology. • Experience in oncology clinical trials or willingness to supervise them. • Minimum 4 years’ experience in independent supervision of all types of visits. • Effective time management, organizational and interpersonal skills and problem-solving skills, with the ability to multi-task and priorities. • Good understanding and working knowledge of clinical research, clinical trial phases, current GCP/ICH and country clinical research legislation and guidelines.
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