Lead CRA, CNS/Oncology - Global Trials (Remote UK)

Remote Worker LTD.; United States; Remote; USD 79,000 - 119,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to lead monitoring activities from start-up to close-out, with potential to Lead CRA on global studies. You will mentor CRAs, contribute to monitoring strategy and work with project teams to ensure data integrity and compliance.

This home-based role supports sites across the United Kingdom, with travel about 6-8 days per month. Strong regulatory knowledge and English proficiency are essential.

Qualifications

• MD or pharmacy-related advanced degree with CRA experience.
• FDA/EU regulations, ICH guidelines, local requirements knowledge.
• Strong knowledge of two to three therapeutic areas.
• Excellent communication, interpersonal, planning and leadership skills.
• Valid passport and driving licence.
• Proficiency in spoken and written English.
• Experience in full-service monitoring preferred.

Responsibilities

• Lead monitoring activities across the study lifecycle including feasibility, pre-study, initiation, interim monitoring and site close-out.
• Serve as Lead CRA on global studies and coordinate CRAs.
• Monitor sites for protocol adherence, patient safety, data quality, informed consent and product accountability.
• Partner with sites to review CRFs, resolve data queries and manage documentation.
• Develop monitoring plans, study tools, templates and training.
• Review site visit reports and mentor less experienced staff.
• Collaborate with Project Management and study teams to evaluate milestones and documentation.
• Contribute monitoring expertise to investigator meetings and bid defenses.

Skills

CRA experience

Regulatory knowledge

English proficiency

MS Office / IxRS / EDC

Team leadership

Education

MD or pharmacy-related advanced degree

Four-year degree in life sciences

Two-year college curriculum in nursing/life sciences

Tools

IxRS

EDC systems

Microsoft Office

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to lead monitoring activities from start-up to close-out, with potential to Lead CRA on global studies. You will mentor CRAs, contribute to monitoring strategy and work with project teams to ensure data integrity and compliance.

This home-based role supports sites across the United Kingdom, with travel about 6-8 days per month. Strong regulatory knowledge and English proficiency are essential.