
Clinical Research Professional
2 weeks ago
A clinical research associate plays a pivotal role in ensuring the protection and well-being of trial participants, as well as the accuracy, completeness, and verifiability of reported trial data from source documents.
Main Responsibilities- Establish and maintain effective relationships with principal investigators, study coordinators, pharmacists, and site trial personnel to ensure efficient management of clinical trials.
- Foster strong customer relationships to support project delivery according to study requirements and timelines.
- Collaborate with internal teams to prepare essential site documents and provide support for ethics and regulatory submission processes.
- Ensure participant recruitment and drive site recruitment initiatives.
- Monitor investigational sites in accordance with ICH GCP guidelines across all phases of a clinical trial.
We are committed to promoting gender equality and creating an inclusive work environment. We offer flexible working options, parental leave, and ongoing development opportunities.
Requirements- Holding a graduate degree in a clinical or life sciences-related field.
- Demonstrating good time management, attention to detail, ability to work effectively in a team, and computer literacy.
- Experience by job level: CRA II – minimum 6 months; CRA III – 2+ years; SCRA – minimum 4 years.
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