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Clinical Research Data Analyst
London, United Kingdom (Hybrid)
Responsibilities:
- Review patient records sourced from various Electronic Health Record (EHR) systems, adhering to provided eligibility criteria, and adeptly map eligible patients with appropriate clinical studies.
- Develop comprehensive summaries based on reviewed patient records and furnish insightful reports on assigned charts.
- Collaborate with external stakeholders, including academic institutions and private enterprises, to initiate novel assignments and
projects to amplify the scope of clinical research.
- Play an integral role in the formulation and documentation of new or refined departmental protocols and guidelines.
- Execute market-based data-driven analyses to identify industry trends and patterns, facilitating the achievement of outcome-based deliverables.
- Analyze and evaluate clinical data to assist in the preparation of strategic presentations, client meetings and project reviews.
Role Requirements:
- Minimum of 2 years of pertinent experience within the clinical/pharmaceutical domain.
- Agility in swiftly navigating across diverse therapeutic domains and indications.
- Proficiency in clinical research methodologies, encompassing regulatory prerequisites and ICH/GCP standards.
- Demonstrated capability in project management from a medical/clinical standpoint, with a proven ability to resolve intricate clinical, medical, and operational challenges.
- Proficiency in the handling and analysis of clinical data.
- Robust project management acumen, coupled with the ability to prioritize tasks and manage multiple responsibilities concurrently.
- Exemplary organizational prowess with acute attention to detail.
- Effective written and verbal communication skills.
- Proficiency in utilizing MS Office suite.
- Flexibility to adapt to evolving project demands and reallocate focus as necessary.