Research Analyst

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborating with investigators and site staff to facilitate smooth study conduct
• Performing data review and resolution of queries to maintain high-quality clinical data
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Clinical Research Associate

• Site administration and site monitoring responsibility for assigned clinical studies according to Dokumeds and Sponsor Standard Operating Procedures, legal requirements and ICH-GCP Guidelines
• Conduct of country and site feasibility
• Site initiation, routine monitoring and close-out visits
• Preparation and submissions to Ethics Committees/Regulatory Authorities
• Assistance in site contract management

Freelance Clinical Research Associate, Germany

• Execute clinical monitoring activities at clinical trial sites
• Monitor clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs
• Collaborate closely with the Country and Regional Clinical Study Teams to ensure study timelines are adhered to and required quality standards are maintained
• Identify gaps and areas for improvement and propose CAPA
• Support start-up activities
• Conduct site selection and evaluation
• Provide protocol and related study training to assigned sites
• Conduct onsite/remote pre-study, initiation, routine monitoring and closeout visits per monitoring plan
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans
• Manage sites and site performance by tracking regulatory submissions, recruitment, case report form completion, and data query resolution
• Ensure inspection readiness of study and sites

• Perform in-depth static software analysis using newly developed tools for native iOS applications
• Identify defects and anomalies in analyzed software and assess software quality attributes
• Adapt and apply analysis approaches to target platforms and implement them in practice
• Contribute original ideas and research new methods

Research Associate – Software Analysis

• Ensure real estate data collection and update of existing databases (office, industrial, retail, residential, hotel, investment etc.) to deliver regular market and economic updates
• Cooperate with other business services teams to gather, analyse, and utilize local and regional market insights, including competitive, client, and industry data, to produce market thought leadership
• Support business development activities, including presenting market updates to clients
• Undertake independent market analyses for ad-hoc reports for clients as defined by the business
• Support marketing and communication activities in line with the company content strategy defined by the Head of Business Development Services, Germany
• Contribute to C&W brand visibility through active participation in public events and social media
• Cooperate with C&W research teams in other countries and the wider EMEA team

Senior Research Analyst

• Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices
• Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through database lock, ensuring relevant timelines and quality deliverables are met
• Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
• Monitor site level AEs and SAEs and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution
• Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development and checks, when applicable

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