Clinical Research Associate South East

We are building something EPIC
.

Evestia Clinical is a biotech-focused global CRO delivering authentic expertise and personalized support. We partner with clients to provide expert guidance through complex clinical trials in specialized areas, including Rare Disease, Oncology, Neurology, and Immunology. Here, you become a vital part of a global team delivering life-changing impact through clinical excellence.

Our foundation is built on principles that define our identity.
Innovation drives us to seek new solutions, while Excellence ensures high standards in every project. This is balanced by genuine Care
, fostering a supportive culture for both our patients and our people. Above all, we champion Partnership
, believing that working together— with trust and flexibility —is the key to our collective success.

Our approach is agile and personalized, empowering you to find creative solutions. We offer a welcoming culture that values belonging, ensuring you have the environment needed to thrive and grow. If you are ready to change lives worldwide, join our team.

Evestia Clinical is looking for a Clinical Research Associate (II or Senior) in the North West to be responsible for ensuring that the rights and safety of clinical trial participants are protected and that the clinical data obtained are accurate, complete, and verifiable according to source.

• Perform all visit types while ensuring regulatory and protocol compliance
• Participate in all aspects of a clinical trial from development and planning to study closure
• Comply with applicable regulations, ICH/GCP and Evestia Clinical or sponsor SOPs to assess the safety and efficacy of investigational products (drugs, biologics or devices)
• Maintain key performance metrics in accordance with company standards and timelines, ensuring compliance with established monitoring and reporting expectations
• Ensure assigned sites are in compliance with the study protocol objectives
• Work in project teams and under supervision, reporting to a Clinical Team Lead and/or Project Manager
• Liaise effectively between sponsors, investigators and project teams
• Complete all administrative tasks (expense and time reporting) within company guidelines
• Perform any other duties as assigned

• Substantial previous experience independently monitoring and performing all types of site visits
• Ideally based in the South East
• Understanding the principles of Good Clinical Practice (GCP) and clinical trial regulations
• Both written and verbal communication and presentation skills
• Understanding of medical terminology and human physiology
• Proficiency with information technology (computer skills)
• Excellent customer service skills
• Demonstrated flexibility and adaptability
  
  Ability to work in a team environment and independently as needed
• Ability to travel nationally and internationally as required
• Organizational and time management skills, able to prioritize tasks and work within timelines

We believe that to do your best work, you need the best support. That’s why we care deeply about your well‑being, personal development, and achieving a true work‑life balance. Our comprehensive benefits package is carefully designed to align with our culture and values, ensuring it maximizes your positive experience working here.

• Health Insurance: 99% employer-paid
• Dental & Vision Insurance: 100% employer-paid
• Short‑Term & Long‑Term Disability: 100% employer-paid
• Life Insurance Policy
• 401(k) Retirement Plan: 3% employer contribution
• Flexible and Hybrid Work Options
• Unlimited PTO for salaried staff
• 12 Corporate Holidays
• Employee Assistance Program (EAP)
• Wellness Program
• Learning & Development Stipend:
  Increases with tenure
• Charitable Match Program
• Wednesdays Catered Lunches (In-Office)

Does joining Evestia Clinical and making a global impact excite you? Then it's time to apply!

We are eager to meet ambitious candidates. Remember, we hire for potential and passion. Therefore if you feel you’re a good fit but don’t meet every single requirement, please submit your application anyway. We want to hear from you.