About the role
Job Description
As a Clinical Research Associate I you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.
You will:
* Conduct and report all types of onsite monitoring visits * Be involved in study startup (if applicable) * Perform CRF review, source document verification and query resolution * Be responsible for site communication and management * Be a point of contact for in-house support services and vendors * Communicate with internal project teams regarding study progress * Participate in feasibility research * Support regulatory team in preparing documents for study submissions
Qualifications
* College/University degree in Life Sciences or an equivalent combination of education, training & experience * Clinical Research or Medical experience * Independent on-site monitoring experience in the UK * PC skills to be able to work with MS Word, Excel and PowerPoint * Ability to plan, multitask and work in a dynamic team environment * Communication, collaboration, and problem-solving skills * Ability to travel * Valid driver’s license
Additional Information
Become a full-fledged clinical research professional with the support of a knowledgeable and professional team. You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.