
Clinical Trials Specialist
Há 3 dias
This is an exciting opportunity to work as a Clinical Research Associate II. The successful candidate will 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:
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials with diligence and attention to detail.
- E nsure protocol compliance, data integrity, and patient safety throughout the trial process by closely following regulatory requirements.
- Collaborate effectively with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
- Bachelor's degree in life sciences, nursing, pharmacy, or a related field. Advanced degree preferred.
- Experience as Clinical Research Associate and with on-site monitoring activities.
- In-depth knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
- Strong leadership and mentoring skills, with the ability to manage and motivate CRAs and site staff effectively.
- Excellent communication, organizational, and problem-solving skills, with a proactive approach to managing site performance and resolving issues.
- Advanced level of English.
- A competitive salary.
- An annual leave entitlement.
- A range of health insurance offerings to suit your needs.
- Competitive retirement planning offerings.
- A Global Employee Assistance Programme offering 24-hour access to a global network of professionals who are there to support you.
- Life assurance.
- Flexible country-specific optional benefits.
We're committed to providing an inclusive and accessible environment for all candidates. We welcome applications from talented individuals who share our values and are passionate about their work.
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