Remote Clinical Research Associate II/Senior Opportunity
We are seeking an experienced and skilled Clinical Research Associate II/Senior to join our team in a remote capacity. As a Clinical Research Associate, you will be responsible for conducting on-site monitoring visits at investigator sites to ensure compliance with Good Clinical Practices (GCP) and applicable regulatory requirements.
Key Responsibilities:
* Conduct on-site monitoring visits to investigate sites, ensuring adherence to GCP and regulatory requirements.
* Maintain strong relationships with investigators, site staff, and other stakeholders to facilitate successful study execution.
* Monitor and manage the progress of studies, identifying and mitigating potential risks and issues.
* Collaborate with cross-functional teams to develop strategies for addressing site-level issues.
* Evaluate clinical trial documentation, reports, and other deliverables for accuracy and timeliness.
Requirements:
* Bachelor's degree in healthcare/life science or related field.
* Significant experience as a Clinical Research Associate from a CRO, pharmaceutical, or biotechnology setting.
* Minimum 2+ years of independent monitoring experience.
* Oncology experience is preferred.
* Excellent communication and interpersonal skills for effective collaboration.
Preferred Qualifications:
* Advanced degree (Master's or Doctoral level) in healthcare/life science or related field.
* Certification in Clinical Research Associate (CRA) or related fields.
* Experience working with electronic data capture (EDC) systems and clinical trial technologies.
Benefits:
* Competitive salary.
* Car allowance.
* Bonus opportunities.