Remote CRA: Site Monitoring, Data Integrity & Compliance

Placements24; United States; Remote; USD 70.000 - 110.000; Vollzeit

Benefits dieser Stelle

Competitive salary and bonuses

Medical, dental, and vision coverage

Retirement savings plan

Generous leave and holidays

Home office equipment allowance

Flexible work schedule

Zusammenfassung

Placements24 is seeking a dedicated Clinical Research Associate for a fully remote role. You will monitor clinical trial sites, verify data integrity, and ensure regulatory compliance across multiple studies from a distributed team.

The ideal candidate holds a life science degree with at least 3 years of CRA experience, strong knowledge of GCP/ICH, and proficiency in EDC/CTMS. This remote-first role offers flexibility and opportunities for professional development.

Qualifikationen

• Bachelor's degree in life science, nursing, or related discipline.
• Minimum of 3 years of direct CRA experience.
• Knowledge of GCP, ICH guidelines, and regulatory requirements.
• Experience managing multiple trials and sites.
• Proficiency with EDC, CTMS and related software.

Aufgaben

• Conduct site visits (initiation, monitoring, close-out) via remote tools.
• Verify data accuracy and compliance using source documents and EDC.
• Ensure adherence to GCP, SOPs and study protocols.
• Serve as primary contact for assigned sites.
• Manage site recruitment and enrollment with investigators.
• Prepare study documents for regulators and IRBs/ECs.
• Monitor subject safety and report AEs/SAEs.
• Oversee study drug accountability at sites.
• Communicate with project teams (managers, data managers, investigators).

Kenntnisse

Organizational skills

Analytical abilities

Problem-solving

Communication skills

Interpersonal skills

Remote collaboration

Ausbildung

Bachelor's degree in life science or related field

Tools

EDC systems

CTMS

Clinical research software

Jobbeschreibung

Placements24 is seeking a dedicated Clinical Research Associate for a fully remote role. You will monitor clinical trial sites, verify data integrity, and ensure regulatory compliance across multiple studies from a distributed team.

The ideal candidate holds a life science degree with at least 3 years of CRA experience, strong knowledge of GCP/ICH, and proficiency in EDC/CTMS. This remote-first role offers flexibility and opportunities for professional development.