Senior CRA - Oncology & Hematology | Remote

Worldwide Clinical Trials; Barcelona; Remote; EUR 60,000 - 80,000; Full time

Job summary

Worldwide Clinical Trials in Spain is seeking a Senior Clinical Research Associate to protect patient safety, ensure data quality, and adhere to GCP, regulations, protocols, and SOPs. You will own full monitoring lifecycle from qualification to close-out, mentor CRAs, and collaborate with study teams while traveling to investigative sites about 8-10 days per month.

This home-based role requires English and local language fluency, and a strong background in clinical research and two to three

Qualifications

• MD/Pharmacy with CRA experience of 3+ years, or equivalent science degree with 5+ years CRA experience.
• Strong knowledge of FDA/EU regulations, ICH guidelines, and SOPs.
• Excellent communication and leadership abilities, with willingness to travel.

Responsibilities

• Lead site qualification, initiation, interim monitoring, management, and close-out activities.
• Protect patient safety and data integrity by reviewing informed consent and safety information, conducting source document verification, reviewing CRFs, and supporting timely query resolution.
• Guide sites in protocol adherence, Investigator Site File maintenance, regulatory and ethics documentation, investigational product accountability, and ongoing study requirements.
• Coordinate CRAs as a Lead CRA on global studies and provide mentoring, training, accompanied visits, and practical guidance to less experienced colleagues and site staff.
• Partner with Project Management and study teams to evaluate deliverables, study milestones, site performance, and monitoring activities.
• Develop monitoring plans, study-specific tools, templates, and training materials as requested to support consistent study delivery.
• Review site visit reports and provide feedback while maintaining site documentation for the Trial Master File.
• Contribute your clinical monitoring expertise to study team and investigator meetings, bid defenses, and the design of protocols and CRFs.

Skills

CRA experience

Regulatory knowledge

Communication

Leadership

EDC/IxRS

Travel readiness

Education

MD or Pharmacy qualification

Nursing or related science degree

Tools

Microsoft Office

IxRS

EDC systems

Job description

Worldwide Clinical Trials in Spain is seeking a Senior Clinical Research Associate to protect patient safety, ensure data quality, and adhere to GCP, regulations, protocols, and SOPs. You will own full monitoring lifecycle from qualification to close-out, mentor CRAs, and collaborate with study teams while traveling to investigative sites about 8-10 days per month.

This home-based role requires English and local language fluency, and a strong background in clinical research and two to three