Senior Clinical Research Associate, Medical Device
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Senior CRA monitoring orthopedic medical-device trials for ICON Strategic Solutions. Overseeing sites, compliance, data integrity, and trial execution across Midwest/West regions.
Responsibilities:
- Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
- Lead clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement
- Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
- Conduct site visits to assess site performance, resolve issues, and support successful trial execution
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Provide training and guidance to site staff and other CRAs
- Build and maintain relationships with site personnel and stakeholders
- Manage multiple sites and projects simultaneously
Requirements:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- 3-5 years of CRA monitoring experience in CRO/pharma environments
- Strong CRA experience managing complex protocols
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously
- Expertise in monitoring practices, data integrity, and site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills
- Willingness to travel as required (approximately 60%)
- Limited Canadian travel may be required
- Legal right to work in the country where the role is based
Benefits:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Similar Jobs
Business Development Director – Clinical Research
Business Development Director driving CRO sales and strategic accounts for Ergomed, a clinical research and pharmaceutical services group. Developing partnerships across the UK and Nordic markets.
Clinical Research Associate II – French Speaking
Clinical Research Associate monitoring rare disease and oncology trials for Ergomed, a specialist clinical research organization. Conducting site visits, verifying investigator readiness, training staff, and supporting regulatory submissions.
Senior Clinical Research Associate
Senior Clinical Research Associate managing oncology and global clinical trials for Precision for Medicine, a life sciences CRO. Conducting site monitoring, regulatory oversight, and clinical data quality activities.
Clinical Trial Manager I – Sponsor Dedicated
Clinical Trial Manager conducting clinical monitoring and site management for Syneos Health’s biopharmaceutical solutions business. Supporting regulatory compliance, data integrity, recruitment, and trial delivery.
Senior Clinical Data Manager – Sponsor Dedicated
Senior Clinical Data Manager leading sponsor-dedicated clinical data management at Fortrea. Overseeing studies, vendors, budgets, data quality, standards, and client relationships.
Senior Clinical Data Manager
Senior Clinical Data Manager supporting Biogen’s clinical trials through data review, cleaning, reconciliation, and risk management. Providing Clinical Data Management expertise across study teams and vendors.
Senior Clinical Scientist
Senior Clinical Scientist leading HIV clinical trials for ICON Strategic Solutions’ sponsor-dedicated research programs. Managing medical monitoring, protocol execution, data review, and investigator collaboration.
Senior Clinical Trial Manager
Senior Clinical Trial Manager leading early-phase trial operations for Arbor Biotechnologies’ gene-editing therapeutics. Managing sites, CROs, vendors, timelines, budgets, and study execution.
Clinical Research Associate
Clinical Research Associate monitoring clinical trials for Alira Health’s global healthcare research team. Ensuring protocol compliance, site quality, regulatory documentation, and accurate clinical data.
Clinical Research Associate
Clinical Research Associate monitoring clinical trials for Alira Health’s global research team. Ensuring protocol compliance, site quality, data integrity, and regulatory adherence.
Clinical Research Associate
Clinical Research Associate monitoring clinical trials for global healthcare company Alira Health. Ensuring site compliance, data integrity, regulatory adherence, and study quality through remote and onsite visits.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring sponsor-dedicated clinical trials for ICON. Ensuring protocol compliance, site performance, data integrity, and regulatory standards.
Clinical Research Associate
Field-based Clinical Research Associate advancing AbbVie’s innovative medicines through clinical trials. Monitoring sites, ensuring compliance, and supporting patient recruitment and data integrity.
Senior Clinical Trial Manager
Clinical Trial Manager advancing Jade Biosciences’ autoimmune disease therapies through Phase 1–3 trials. Coordinating CROs, budgets, vendors, sites, compliance, and study execution.
Local Clinical Study Manager – Eastern Europe
Clinical Study Manager overseeing oncology and onco-hematology trials for IQVIA across Eastern Europe. Leading clinical teams, site activation, monitoring, regulatory delivery, and study execution.
Senior Clinical Research Associate – CRO-Contract
Contract Senior Clinical Research Associate monitoring clinical trial sites for Lotus Clinical Research. Ensuring GCP compliance, site documentation, investigational product accountability, and study close-out.
Senior Clinical Research Associate – CRO Contract
Contract Senior Clinical Research Associate monitoring clinical-trial sites for Lotus Clinical Research. Ensuring GCP, FDA, ICH, protocol, and study-document compliance through site visits.
Associate Clinical Data Manager – FSP
Associate Clinical Data Manager supporting sponsor-dedicated clinical trials at Fortrea. Managing clinical data queries, study timelines, validation processes, and data management standards.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring sponsor-dedicated Phase I oncology trials at ICON. Managing sites, ensuring GCP compliance, and guiding clinical trial teams.
Senior Clinical Research Associate
Senior Clinical Research Associate overseeing remote Phase I oncology trial monitoring for ICON Strategic Solutions. Managing sites, compliance, data integrity, and CRA guidance.