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As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity. Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.
Job Responsibility
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 trials, at least 5 years
Minimum 5 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