
Clinical Trials Professional
Há 24 horas
We're seeking skilled professionals to join our dynamic team in conducting clinical trials.
As a Clinical Research Associate II, you'll play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
Key responsibilities include:
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- Performing data review and resolution of queries to maintain high-quality clinical data.
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports.
Required skills and qualifications:
- Bachelor's degree in a scientific or healthcare-related field.
- Previous experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
We offer a range of benefits to support your career growth and well-being, including:
- Competitive salary and annual leave entitlements.
- A range of health insurance offerings to suit your needs.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme, LifeWorks.
- Life assurance.
If you're passionate about making a difference in the lives of others, we encourage you to apply. Our inclusive and accessible environment welcomes candidates from diverse backgrounds.
Please submit your application, including your resume and cover letter, outlining your relevant experience and qualifications.
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