About the Company
CCS Global are partnered with a respected leader in clinical research, as they expand their team, we are actively recruiting a Senior or a Lead level Clinical Research Associate to join their team in the midlands region. Our Client is known for its dedication to advancing clinical research and delivering positive patient outcomes. If you’re ready to work with a forward-thinking organisation that offers incredible opportunities for professional growth, this could be your next career move.
About the Role
As a CRA or our Client, you’ll serve as the crucial link between study sites, sponsors, and regulatory authorities across the Midlands. In this role, you’ll have hands-on involvement across diverse therapeutic areas such as oncology, cardiology, CNS, devices and rare diseases and complex trials in gene therapy, helping drive meaningful advancements in clinical research.
The client offer
Diverse Therapeutic Areas to broaden your knowledge by working across multiple therapeutic fields, enhancing your expertise and adaptability.
Long-Term Career Development: Our Client offers a well-defined pathway for career progression and ongoing growth opportunities within the organization.
Excellent approach to local site allocation, and a thought out process to days on site focussing on quality over volume.
Leading Training Programs: Benefit from industry-leading training to stay at the forefront of clinical research practices and technologies.
Responsibilities
* Monitoring and overseeing clinical trials to ensure they meet ICH-GCP guidelines and regulatory standards
* Partnering with site teams to facilitate efficient, compliant study execution
* Providing mentorship to junior CRAs and supporting protocol development
* Engaging in site selection and contributing to successful study delivery
Required Skills
We’re seeking a CRA who:
* Has experience of at least 3 years independent monitoring
* Knows the UK clinical research landscape and brings strong therapeutic area knowledge
* Holds a valid UK driver’s license and full working rights without restrictions
* Has a Bachelors degree in life sciences
* Is meticulous in clinical monitoring, communication, and documentation
To apply please apply with your up to date CV and we will be in touch.