Clinical Research Associate II
PSI CRO
•Remote
About The Position
As a CRA II, 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. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance. This is a remote role.
Requirements
- BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
- Independent on-site monitoring experience in the UK, ideally on multiple projects at a time
- Demonstrable experience in all types of monitoring visits in Phase II and/or III
- Strong written and verbal communication skills
- Intermediate to Advanced knowledge of MS Office
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills are essential
- Full and clean driver's license, and the ability to travel
Nice To Haves
- Experience supporting Oncology studies is beneficial, but not essential
Responsibilities
- Conducting and reporting all types of onsite monitoring visits
- Driving the study startup phase (if applicable)
- Performing CRF reviews, source document verification and query resolution
- Be responsible for site communication and management
- Supervising study activities, timelines, and schedules for each site
- Acting as a point of contact for in-house support services and vendors
- Supporting quality control, such as compliance monitoring and reports review
- Participating in feasibility research
- Supporting the regulatory team in preparing documents for study submissions and regulatory approval
Benefits
- Invests in their professional development and success
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
