Senior Clinical Research Associate - UK (Oncology/CNS)

Worldwide Clinical Trials; England; Hybrid; GBP 42,000 - 58,000; Full time

Job summary

Worldwide Clinical Trials in the United Kingdom is seeking a Clinical Research Associate to manage research activities at sites participating in registries and other non-interventional studies across the full study lifecycle.

You will perform SIVs, train sites, collect regulatory documents, and support contracts/budgets, with travel required. Strong English, organization, and proficiency in MS Office, CTMS and EDC are essential.

Qualifications

• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to details.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS and EDC Systems.

Responsibilities

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, including registries and non-interventional studies.
• Identify potential sites, perform study start-up activities, support contract and budget negotiations, train sites to collect data and report safety events.
• Conduct study initiation visits (SIVs).
• Ensure compliance with informed consent, safety reporting, and regulatory requirements, mostly remotely.

Skills

Interpersonal communication

Organizational skills

Independent work

English proficiency

Education

Bachelor's degree or Nursing degree

Tools

Microsoft Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials in the United Kingdom is seeking a Clinical Research Associate to manage research activities at sites participating in registries and other non-interventional studies across the full study lifecycle.

You will perform SIVs, train sites, collect regulatory documents, and support contracts/budgets, with travel required. Strong English, organization, and proficiency in MS Office, CTMS and EDC are essential.