(Senior) Clinical Research Associate (S)CRA – home-based in Spain

Pharma Professionals; United States; Remote; USD 56,000 - 79,000; Full time

Job summary

Pharma Professionals is seeking a Senior CRA to work remotely on a full-time basis for a rapidly expanding international Clinical Research Organisation. The role involves start-up activities, monitoring visits, and collaboration with vendors from home, supporting projects in Spain.

Candidates should have at least 3 years of on-site monitoring experience, with oncology trials preferred, and fluency in English and Spanish. Willingness to travel as needed is essential to meet project needs.

Qualifications

• Minimum 3 years of on-site monitoring experience.
• Preferred experience in Oncology clinical trials.
• Ability to travel as needed to support project requirements.
• Degree or equivalent in a life science discipline.

Responsibilities

• Conduct start-up activities and monitoring visits.
• Maintain study files, write clinical trial reports and liaise with vendors.
• Review progress of projects and initiate appropriate actions to achieve objectives.
• Participate in development of protocols and Case Report Forms.
• Liaise with CPM to evaluate needs, resources and timelines.

Skills

On-site monitoring

Clinical trials

Oncology trials

Travel readiness

Life sciences degree

Fluent English

Fluent Spanish

Team communication

Education

Life sciences degree

Job description

Our Client is a rapidly growing international Clinical Research Organisation offering an experienced(Senior) CRAopportunity to work from home on full FTE as part of their team inSpain.

Responsibilities:

• Conducting start-up activities and monitoring visits
• Maintaining study files, writing clinical trial reports and liaising with vendors
• Reviewing progress of projects and initiating appropriate actions to achieve objectives
• Participation in the development of protocols and Case Report Forms
• Liaising with CPM to evaluate needs, resources and timelines

Requirements:

• Minimum 3 years of on-site monitoring experience
• Preferred experience in Oncology clinical trials
• Ability to travel as needed to support project requirements
• Degree or equivalent in a life science discipline
• Fluency in English and Spanish
• Strong communication and team work skills