Clinical Research Coordinator
vor 2 Wochen
Clinical/Medical Research (Healthcare & Medical)
Full time
We are excited to announce an opportunity for a Clinical Research Coordinator to join our dynamic team at Nucleus Network.
As the only global phase 1 clinical trials specialist with facilities in both the USA and Australia, we are committed to "advancing medicine and improving lives" by attracting exceptional talent.
Since our founding in 2004, Nucleus Network has successfully conducted over 1500 phase 1 clinical trials for biotechnology and pharmaceutical companies from the USA, Europe, Australia, Japan, South Korea, Taiwan, and China.
Our organization is characterized by our core values, outstanding work culture, dedication to staff development, and commitment to providing an optimal work environment.
Join us on this exciting journey of growth and gain world-class experience working with some of the most innovative biotechnology and pharmaceutical companies globally.
About the role
The Clinical Research Coordinator is responsible for the coordination of assigned clinical trials including participant management, project implementation and project conduct in line with the HREC approved protocol.
The Clinical Research Coordinator (CRC) is an integral part of the Project Management team at Nucleus Network.
As a CRC you will be responsible for the coordination of assigned clinical trials right from the start.
You will create study documents, manage participants throughout the recruitment and on-study periods, facilitate important safety and monitoring processes and ensure that data is entered accurately, and data integrity is maintained.
You will work in an amazing team with diverse knowledge and experience, and a shared goal of delivering projects to a high degree of quality and excellence.
You will be supported with a comprehensive learning and development pathway, offering the capacity to grow your career in the clinical research space.
Key responsibilities
Preparation and maintenance of study documents Liaising with and managing participants on your clinical trials Completion of data entry, data queries & quality assurance checks Pro-actively providing ongoing information to the Project Managers and broader teams to ensure key milestones remain on-track Ensuring studies are conducted in accordance with regulatory and ethical guidelines as well as Nucleus Network Standard Operating Procedures Performing clinical procedures, including vital signs, ECG, and blood collection via cannula and venepuncture (training provided) Requirements
Degree in a relevant scientific discipline Excellent communication, organizational skills and attention to detail Motivated by planning and problem solving, with a solution-focused mindset Able to work in a team environment as well as autonomously Adaptable, able to work well under pressure and willing to take on a challenge Able to work in a dynamic, fast-paced environment that requires a pro-active mindset Able to work in an environment that focal points change at short notice and have the ability to pivot between tasks Willing to perform clinical procedures (full training provided) If you are interested in applying for this position, please include a CV and cover letter with your application.
At Nucleus Network we are committed to creating a supportive and inclusive space where every individual feels they can be their full selves.
Our policy applies to all aspects of employment, including our hiring and selection process.
We are an equal opportunity employer, seeking people from all life stages, backgrounds and life perspectives.
Our focus is on people who embody our values of drive, teamwork, customer focus, and excellence.
At Nucleus Network, we recognize our responsibility to ensure the safety of our staff, participants, and visitors.
As such, Nucleus Network requires all employees to be vaccinated against COVID-19.
Vaccination evidence must be provided before the commencement date.
For further information about Nucleus Network, please go to
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