Life Science People are a strategic growth partner within the Life Science industry providing bespoke services to the life science community from SMEs through to blue-chip organisations and sourcing the best talent to make a tangible contribution to healthcare.
Do you want to work for a company that pushes boundaries, innovates, and invents? A company that are made up of pioneering experts, bright thinkers, dreamers, and doers. If so, then this may be the role for you…
The path to a cure for the world's most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence.
The Clinical Research Associate (CRA), Evidence (Real-World Evidence [RWE]) is responsible for managing the research activities at sites of clinical research projects, which are predominantly registries and other types of non-interventional / observational studies.
The CRA will typically be involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded.
While most of the site management efforts will be performed remotely, some on-site management activities will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements.
- 1.5+ years' of experience as a Clinical Research Associate.
- Bachelor's degree or equivalent education and experience.
- One or more years of experience with Phase IV, Post-Approval, Late Stage, Health Economics and Outcomes Research or Observational Studies strongly preferred.
So, what's next?
If this role interests you, then please apply now. You can submit your CV and cover letter highlighting your expertise as a Clinical Research Associate (CRA). We will send you a confirmation of acknowledgement, and please note feedback can take up to a 1-week.
Upon successful selection, you will have an initial screening call with a Life Science People representative and then an interview with the company directly.
The Clinical Trial Associate role is a full-time permanent position, paying up a competitive salary, a wide range of industry-best benefits that include unlimited PTO, 10 paid holidays and matching 401(k). You will be home-based but will need to have a willingness to travel. Full details will be provided on application.