Clinical Research Associate 1
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
In Vitro Diagnostics CRA conducting clinical research studies for ICON, a global healthcare intelligence and clinical research organisation. Monitoring trials, validating product claims, and supporting regulatory submissions.
Responsibilities:
- Deliver clinical trial monitoring work to a high standard
- Ensure studies are conducted according to study protocols, operating procedures, and good clinical practice
- Validate product performance claims
- Supply data for critical regulatory submissions
- Define the functional and clinical utility of investigational products
- Understand and implement federal regulations
- Help roll out SOPs to ensure studies adhere to FDA regulations, GCP, IVD directives, and client policy
- Work closely with the clinical trial team and stakeholders
- Contribute to initiating, monitoring, and completing clinical research studies for in vitro diagnostics
Requirements:
- University degree in medicine, science, or equivalent
- Relevant in vitro diagnostics experience, ideally from a laboratory background
- Practical knowledge of in vitro diagnostics and clinical trial processes
- Excellent written and verbal communication in English
- Good social skills enabling timely handling of queries
- Willingness to travel as required from a UK base, occasionally internationally
- 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
- Reasonable accommodations during the recruitment process
Similar Jobs
Cybersecurity Research Specialist
Cybersecurity research specialist evaluating AI-generated vulnerability, exploit, and defensive-security reasoning for 24-MAG. Developing expert benchmarks for advanced AI cybersecurity capabilities.
Clinical Research Associate I
Clinical Research Associate advancing AbbVie’s innovative medicines through clinical-trial site monitoring. Supporting investigator sites, recruitment, compliance, data integrity, and patient safety across the US.
Research Regulatory Specialist – National Center for Clinical Trials
Research Regulatory Specialist supporting IRB, FDA, and clinical-trial compliance for Advocate Health’s National Center for Clinical Trials. Preparing submissions, maintaining audit-ready records, and training research staff.
Research Solutions Analyst
Research Solutions Analyst delivering legal, regulatory, litigation, and competitive intelligence for Eversheds Sutherland, a global law firm. Building automated monitoring and AI-enabled knowledge solutions for attorneys and business professionals.
Clinical Research Associate II/Sr
Clinical Research Associate monitoring clinical trial sites for Parexel, a global CRO delivering life-changing medicines. Managing site relationships, documentation, compliance, and audit readiness across studies.
Lead Clinical Research Associate
Lead Clinical Research Associate overseeing country-level trial quality, compliance, monitoring, and clinical teams for PSI, a contract research organization. Providing remote study oversight across clinical research activities in Colombia.
Lead Clinical Research Associate
Lead clinical research trials for PSI, a contract research organization, across Peru and regional teams. Oversee monitors, compliance, data integrity, training, audits, and study delivery remotely.
Lead Clinical Research Associate
Lead Clinical Research Associate overseeing country-level trial quality, compliance, monitoring, and team coordination remotely for PSI, a contract research organization.
Clinical Research Associate
Clinical Research Associate monitoring early-development clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Conducting site visits, ensuring ICH-GCP compliance, and maintaining data integrity and patient safety.
Clinical Research Associate II
Clinical Research Associate monitoring clinical studies for Precision for Medicine, a CRO integrating trial execution with scientific, laboratory, and data-science expertise. Coordinating site setup, regulatory submissions, initiation visits, compliance, and risk mitigation across Belgium and the Netherlands.
Clinical Research Associate II
Clinical Research Associate monitoring clinical trials in Belgium for a life-sciences CRO. Ensuring compliant site execution, study progress, regulatory submissions, and risk mitigation.
Research Specialist
Research Specialist responsible for creating client reports and market research for US Sales Enablement team. Engaging with diverse teams and mentoring junior analysts for effective project delivery.
Clinical Research Associate II
Clinical Research Associate II responsible for global study implementation in Germany. Join AbbVie to improve global healthcare managing clinical trials in a dynamic research environment.
Clinical Research Associate II – Full-time, 24-month fixed-term
Clinical Research Associate II at AbbVie leading global drug studies in Germany. Managing study execution, coordination, and compliance for clinical trials through collaborative efforts.
Compliance Research Associate
Compliance Research Associate responsible for executing research projects for the Democratic National Committee. Focused on social media research and vetting using LexisNexis databases.
Technical Research and Development Specialist – R&D
Technical Research & Development Specialist handling R&D assessments for Australian professional services firm. Engaging in technical uncertainty discovery and analysis through AI-assisted workflows.
Research Analyst
Research Analyst supporting community-engaged research, program evaluation, and quality improvement initiatives. Focus on Federally Qualified Health Centers and improving health outcomes and equity.
Quantitative Research Associate, International Development
Quantitative Research Associate supporting international development projects by managing data and conducting analyses. Collaborating with major international donors for innovative policy designs.
Senior Clinical Research Associate
Senior Clinical Research Associate managing drug trials for an innovative life sciences company. Responsible for oversight, support, and documentation throughout clinical trial processes.
Clinical Research Associate – Internal Site Management
Clinical Research Associate ensuring Good Clinical Practice compliance through site monitoring for clinical trials. Collaborating with cross-functional teams and managing site communications effectively.