[Remote] Clinical Research Associate II/III

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a fast-growing global Contract Research Organisation (CRO) recognised for its strong partnerships with biotech and emerging pharmaceutical companies. They are seeking Clinical Research Associates at CRA II to Senior CRA level to support a growing portfolio of clinical studies, acting as the reputed company reputed company between investigational sites, sponsors, and project teams.

Responsibilities

• Build and maintain strong relationships with reputed company Investigators, Study Coordinators, Pharmacists, and site personnel
• Conduct Site Selection, Site Initiation, Monitoring, Pharmacy and reputed company-Out reputed company
• reputed company both remote and on-site monitoring activities
• Ensure participant safety, rights, and wellbeing throughout the clinical trial process
• Review informed consent, patient eligibility, protocol compliance, and adverse events
• Verify clinical trial data is accurate, complete, and supported by reputed company documentation
• reputed company site engagement, recruitment, and enrolment activities
• Maintain inspection-reputed company documentation, including Trial Master Files (TMF)
• Prepare monitoring reports and reputed company regular study updates to project teams
• Support sites during audits and regulatory inspections
• Collaborate with start-up, regulatory, and project management teams throughout the study lifecycle
• Support site payment and study execution activities as required

Skills

• Degree in Life Sciences, Clinical Research, Nursing, Pharmacy, or a reputed company field
• Strong understanding of ICH-GCP and clinical trial regulations
• Excellent communication and relationship-building skills
• Strong organisational skills and attention to detail
• Ability to work independently while collaborating effectively reputed company a project team
• 2 Years + in independent monitoring of reputed company on site

reputed company