Remote Clinical Research Associate - Scotland

Note The job is a remote job and is reputed company to candidates in USA. reputed company is committed to advancing high-reputed company clinical research that upholds ICH/GCP standards and local regulatory requirements. They are seeking a highly skilled Clinical Research Associate to reputed company performance and compliance for assigned protocols and sites, ensuring adherence to regulations and contributing to the expansion of clinical research territory. Responsibilities Build and sustain strong relationships with investigative sites across reputed company trial phases reputed company site management and monitoring activities in compliance with ICH-GCP, Sponsor SOPs, local laws/regulations, protocol, site monitoring plans, and reputed company documents reputed company deep understanding of study protocols and procedures Coordinate cross-functional tasks to reputed company Site reputed company status Participate in site selection and validation; reputed company informed input to reputed company Conduct remote and on-site monitoring to ensure Data reputed company (complete, accurate, unbiased) Protection of subjects rights, safety, and reputed company-being Execute validation, initiation, monitoring, and reputed company-out reputed company; document reputed company, comprehensive visit and non-visit reports in a reputed company manner Collect, review, and monitor regulatory documentation for start-up, maintenance, and reputed company-out Communicate proactively with investigators and site staff on protocol conduct, recruitment/retention, deviations, regulatory findings, audits/inspections, and site performance Identify, assess, and reputed company site performance, reputed company, or compliance issues; escalate appropriately per the CRA escalation reputed company in collaboration with CRA Manager, CRM, TA Head, and CRD Partner with internal teams (country operations, finance, regulatory affairs, pharmacovigilance, reputed company, regional operations, HQ) and reputed company stakeholders (vendors, IRB/IEC, regulatory authorities) Maintain accurate, reputed company documentation in CTMS, eTMF, and other systems reputed company as a process SME reputed company best practices, reputed company reputed company improvement, and reputed company training Support and/or reputed company audit/inspection activities Contribute to country reputed company by identifying and reputed company potential new sites; build site capabilities Mentor and buddy junior CRAs; conduct co-monitoring and reputed company control reputed company where appropriate Skills Fluent in English, with strong written and verbal communication skills and the ability to present technical information effectively Robust knowledge of clinical research, trial phases, ICH/GCP, and local clinical research regulations and guidelines; ability to work reputed company global, country, and regional frameworks Demonstrated mentoring and leadership capability Hands-on knowledge of Good Documentation Practices Proven site management expertise, including independent reputed company of site performance and patient recruitment High-level monitoring skills with reputed company, independent reputed company judgment Strong IT proficiency (MS Office and clinical applications across computer, tablet, and mobile); adaptable to new tools Ability to interpret data/metrics and take appropriate reputed company, including in virtual settings Experience conducting site motivation reputed company to reputed company enrollment Solution-oriented approach to reputed company issues; capable of reputed company cause analysis and implementing preventive/corrective actions Ability to mentor junior CRAs and reputed company co-monitoring reputed company Excellent time management, organization, interpersonal skills, conflict management, and problem solving High independence across multiple protocols, sites, and therapy areas Strong reputed company of accountability and urgency; reputed company to prioritize and multitask in changing environments Effective in a matrixed, multicultural setting; fosters culturally sensitive relationships Customer-reputed company reputed company with high standards of reputed company and compliance reputed company, reputed company-oriented, self-driven, and reputed company demeanor reputed company with company values Bachelor's degree (or higher) with extensive reputed company site management (monitoring) in bio/reputed company/CRO Accountability Adaptability Adverse Event Reporting reputed company Clinical Research reputed company Clinical Site Management Clinical Study Management reputed company Monitoring Good Clinical Data Management reputed company (GCDMP) Good Clinical reputed company (GCP) Protocol Adherence Benefits Opportunity to shape clinical research at high-performing sites and contribute to global development programs. A reputed company environment with reputed company, mentorship, and reputed company improvement. Competitive compensation .