Job Description

Entry Level - Clinical Research Associate
London, United Kingdom
Clinical Research Associate
PCD320181

Job Summary

Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. Individuals who have succeeded in the CRA role include:

Nurses
Dieticians
Pharmacy Technicians
Pharmaceutical/Device Sales Representatives
Biotech Engineers
PhD/Pharm.D candidates
Health and Wellness Coordinators
Site Coordinators, Clinical Research Coordinators
Research Assistants.

UNEXPECTED REWARDS

This role takes you on a journey through travel and excitement which will allow you to make a difference on a large-scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:

Dynamic working environment, with varying responsibilities day-to day.
Expansive experience in multiple therapeutic areas.
Work within a team of therapeutic and regulatory experts.
Defined CRA promotion and growth ladder with potential for mentoring and management advancements.
Competitive pay and bonus program.

Responsibilities

Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, public cloud platform and applicable regulatory requirements;
Verification that the investigator is enrolling only eligible subjects;
Regulatory document review;
Medical device and/or investigational product/drug accountability and inventory;
Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement;
Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

Minimum of a bachelor’s degree; Health or life science related field preferred;
Willing to travel approximately 60-80% nationally;
Familiarity with enterprise technology vendor® Office; and.
Strong communication and presentation skills a plus.
Must hold a valid drivers licence.
Willing to be fully office based during the core training program.