Remote Clinical Research Associate: Drive Life-Saving Trials

Placements24; United States; À distance; USD 75 000 - 110 000; Plein temps

Résumé du poste

Placements24 is seeking an experienced Clinical Research Associate (CRA) for a fully remote role. You will monitor trial sites, ensure data integrity and patient safety, and ensure adherence to protocols and regulatory requirements.

The ideal candidate has 3+ years’ CRA experience, strong knowledge of GCP and ICH guidelines, and proven ability to manage multiple sites remotely. Travel may be required occasionally, with a focus on delivering high-quality clinical data.

Qualifications

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field.
• Minimum 3 years of experience as a Clinical Research Associate (CRA) or equivalent.
• Thorough understanding of clinical trial processes, GCP, and ICH guidelines.
• Experience in monitoring multiple clinical trial sites.
• Excellent communication, interpersonal, and organizational skills.
• Ability to work independently and manage time effectively in a remote setting.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness to travel occasionally if required for specific site meetings or audits (though primarily remote).

Responsabilités

• Conduct site visits (initiation, monitoring, and close-out) according to protocol and company SOPs.
• Assess protocol and CRF (Case Report Form) compliance by reviewing source documents.
• Ensure the safety and rights of trial subjects are protected and that trial data are accurate, complete, and verifiable.
• Train and manage, through guidance, other appropriate individuals at the site, e.g., the Study Coordinator.
• Build and maintain a positive relationship with the site staff and investigators.
• Manage study sites, ensuring timely recruitment and data collection.
• Prepare monitoring visit reports and elevate site issues as necessary.
• Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, and all applicable local regulations.
• Oversee the quality and integrity of data submitted from clinical trial sites.

Connaissances

GCP knowledge

ICH guidelines

CTMS

EDC systems

Site monitoring

Formation

Bachelor's degree in Life Sciences

Outils

CTMS

EDC systems

Description du poste

Placements24 is seeking an experienced Clinical Research Associate (CRA) for a fully remote role. You will monitor trial sites, ensure data integrity and patient safety, and ensure adherence to protocols and regulatory requirements.

The ideal candidate has 3+ years’ CRA experience, strong knowledge of GCP and ICH guidelines, and proven ability to manage multiple sites remotely. Travel may be required occasionally, with a focus on delivering high-quality clinical data.