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Clinical Research Professional with Site Management Experience
3 semanas atrás
Job Title: Clinical Research Associate
Overview of the JobWe are seeking an experienced Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for identifying, selecting, initiating, and closing out investigational sites for clinical studies in phases II - IV.
Responsibilities- Set up and monitor studies, complete reports, and maintain documentation
- Submit protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
- Balancing sponsor generated queries
- Taking responsibility for study cost efficiency
- Preparation and review of study documentation and feasibility studies for new proposals
- Potential to assist in training and mentoring fellow CRAs
- 18 months+ of monitoring experience in phase I-III trials as a CRA
- College degree in medicine, science, or equivalent
- Previous monitoring experience in medium-sized studies, including study start-up and close-out
- Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
- Excellent written and verbal communication
- Ability to work to tight deadlines
- Availability to travel least 60% of the time (international and domestic)
- Very competitive salary packages
- Range of health-related benefits to employees and their families
- Competitive retirement plans
- Life assurance
We have a culture that rewards high performance and nurtures talent. We believe in providing a workplace free of discrimination and harassment.
