Clinical Research Associate

1 week ago

London, United Kingdom Icon plc Full time

**We are hiring for CRA across UK (Homebased)**:
**Overview**:
As Clinical Research Associate you will be responsible for maximizing site performance and site engagement in our client conducted clinical studies, as well as leveraging strong clinical operational and therapeutic expertise (scientific, clinical, disease states, and treatment alternatives knowledge within the therapeutic area(s)) to support execution of the clinical studies.

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

**RESPONSIBILITIES**:
**What you will be doing**:

- Responsible for the planning, initiation, coordination and management of all monitoring and monitoring-related activities as well as supervision of all site-related activities to ensure compliance with the client Standard Operating Procedures (SOPs), Good Clinical Practices (GCP) and regulatory requirements
- Engage with clinical sites to develop, build, and maintain strong relationships with investigators/staff that will ensure high quality investigative sites to support the client’s clinical development programs
- Collaborate with internal and external stakeholders as well as third party vendors
- Provide operational support to the CPM/Sr CPM to deliver the study within planned timelines and according to required standards of quality and compliance
- Evaluate, screen and develop high quality investigative sites to support the client’s clinical development programs
- Responsible for the early engagement with Key Opinion Leaders (KOLs)/ sites / patients organizations and key contact point for these throughout the study.
- Interact/train new investigators to work on the client clinical trials
- Attend key therapeutic trainings/meetings and/or industry trainings

**QUALIFICATIONS**:
**You are**:

- A CRA with a minimum of 2+ years of monitoring experience in UK.
- Excellent verbal and written communication in English
- Operate effectively within an international and rapidly changing environment
- Ability to supervise monitoring and related activities in a clinical trial
- Ability to have scientific discussions with Investigators and Site Personnel
- BA/BS Degree required

Pay: From £50,000.00 per year

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