Job Description
We are a leading global life sciences company.
As a Clinical Research Associate II, you will have the opportunity to advance healthcare and make a difference in people's lives with your ideas and unique perspective.
You will be responsible for monitoring Phase I - IV clinical trials, conducting routine study site monitoring visits, and closing out clinical sites.
Key Responsibilities:
* Monitor all aspects of study site operations, including routine monitoring and close-out of clinical sites
* Participate in pre-study qualification and site initiation visits
* Conduct routine study site monitoring visits
* Closely manage clinical sites to maintain the success of studies
Responsibilities Continued:
* Implement process improvements to increase efficiency and effectiveness of clinical research operations
* Identify and escalate any issues that may impact the success of studies
Requirements:
* University or college degree, or certification in a related allied health profession from an appropriately accredited institution
* Thorough knowledge of regulatory requirements and the drug development process
* Intermediate to advanced clinical monitoring experience
* Strong understanding of Serious Adverse Event (SAE) reporting and registry administration skills
Benefits:
* Career progression and opportunities for advancement
* A competitive remuneration package
* A friendly and inclusive team environment
Our organization is committed to providing flexibility and work-life balance. If you are passionate about Clinical Research and have relevant experience, we encourage you to explore this opportunity.