Impactful Clinical Research Associate - Sweden

ThermoFisher Scientific; Sweden; Remote; SEK 520,000 - 750,000; Full time

Job summary

PPD, part of Thermo Fisher Scientific, is seeking a Clinical Research Associate to monitor sites and ensure data integrity across studies. You will apply risk-based monitoring, SDR/SDV review, regulatory compliance, and communicate findings to the clinical team.

Education, English fluency and a science degree are required; you should be comfortable with ICH-GCP, EU/FDA regulations, and have a valid driver’s license.

Qualifications

• University degree in science field.
• Understanding of ICH-GCP, EU and FDA requirements.
• Fluency in English.
• Valid driver's license.

Responsibilities

• Monitors investigator sites using risk-based approach and identifies corrective actions.
• Ensures data accuracy through SDR, SDV and CRF review during monitoring activities.
• Assesses investigational product via inventory and records review.
• Documents observations in reports per timelines and standards.
• Escalates issues to clinical management and follows through to resolution.
• Participates in investigator payments and in team issue resolution.
• Participates in investigator meetings to identify qualified sites.
• Initiates sites per protocol, ensuring compliance with regulatory requirements.

Skills

Monitoring skills

ICH-GCP knowledge

English fluency

Problem solving

Risk-based monitoring

Communication

Team collaboration

Attention to detail

Education

University degree in science

Tools

Microsoft Office

Job description

PPD, part of Thermo Fisher Scientific, is seeking a Clinical Research Associate to monitor sites and ensure data integrity across studies. You will apply risk-based monitoring, SDR/SDV review, regulatory compliance, and communicate findings to the clinical team.

Education, English fluency and a science degree are required; you should be comfortable with ICH-GCP, EU/FDA regulations, and have a valid driver’s license.