About The Position
As a Clinical Research Associate I, you will communicate with project stakeholders and help ensure timelines, targets, and standards are met across clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators, with a focus on subjects’ rights, safety, and well-being, as well as data quality and compliance. The role includes onsite monitoring, study startup activities where applicable, site management, and collaboration with internal teams and support services. You will receive support from a knowledgeable and professional team and develop a variety of skills while progressing with the company and contributing to challenging, full-scale projects.
Requirements
- College or university degree in Life Sciences, or an equivalent combination of education, training, and experience.
- Clinical research or medical experience.
- Independent onsite monitoring experience in the UK.
- PC skills to work with MS Word, Excel, and PowerPoint.
- Ability to plan and multitask in a dynamic team environment.
- Communication, collaboration, and problem-solving skills.
- Ability to travel.
- Valid driver’s license.
Responsibilities
- Conduct and report all types of onsite monitoring visits.
- Participate in study startup, if applicable.
- Perform CRF review, source document verification, and query resolution.
- Manage site communication and site relationships.
- Serve as a point of contact for in-house support services and vendors.
- Communicate study progress to internal project teams.
- Participate in feasibility research.
- Support the regulatory team in preparing documents for study submissions.
Benefits
- Support from a knowledgeable and professional team.
- Opportunities to develop a variety of skills and progress with the company.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
