Jr. Clinical Trials Data Specialist
TempusSalary not specified
Full Time
Entry Level & New Grad, Junior (1 to 2 years)
Not SpecifiedCompensation
Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Clinical Trials, Healthcare Technology, BiotechnologyIndustries
Requirements
Candidates should have 3+ years of experience developing systems and procedures to store, organize, validate, and manage clinical trial data in an academic or commercial setting, and thrive in a startup environment. They should also enjoy working in a multidisciplinary team and bring creative thinking, attention to detail, and empathy for patients to data management, with experience in CDISC standards (SDTM) being a plus.
Responsibilities
The Data Manager will become an expert on the electronic data capture (EDC) capabilities of Citrus, act as the data management lead for multiple trials simultaneously, ensure the highest quality outcome data for a trial from an early design stage, create and contribute to trial design documents (data management plans), design CRFs and questionnaires for efficient and user-friendly data collection, develop processes to test trial implementation and support clinical operations with user acceptance testing (UAT), support ongoing live trials with data-related expertise (data queries, change control), and provide data extracts and reports.
Skills
Data Management
Clinical Trials
Data Validation
Data Organization
CDISC standards
SDTM
Electronic Data Capture (EDC)
Data Management Plans
CRF Design
User Acceptance Testing (UAT)
Data Queries
Data Extracts
Reporting
Lindus Health
Accelerates clinical trials for life sciences
About Lindus Health
Lindus Health focuses on speeding up clinical trials to help patients access new treatments more quickly. The company operates differently from traditional contract research organizations (CROs) by using a fixed-price model for studies and milestone-based payments, which aligns their incentives with those of their clients. Lindus Health combines a skilled clinical operations team with a specialized software platform and access to a vast database of 30 million Electronic Health Records. They handle all aspects of clinical studies, including designing the study, recruiting patients, capturing clinical data, monitoring progress, and managing projects. With their approach, Lindus Health has successfully assisted over 90 sponsors in conducting clinical trials across the US, UK, and Europe, completing them up to three times faster than conventional CROs and often delivering results ahead of schedule.
London, United KingdomHeadquarters
2021Year Founded
$23MTotal Funding
SERIES_ACompany Stage
Biotechnology, HealthcareIndustries
51-200Employees
Benefits
Health Insurance
Unlimited Paid Time Off
Flexible Work Hours
Mental Health Support
Enhanced Parental Leave
Professional Development Budget
Cycle to work scheme
Stock Options
Regular team events
A new laptop as your main workstation
Risks
AI-driven diagnostics could challenge Lindus Health's market position in clinical trials.
Rapid pathogen evolution in infectious disease trials requires continuous adaptation and innovation.
Demand for diverse patient populations may strain recruitment capabilities in less diverse regions.
Differentiation
Lindus Health accelerates trials using a unique software platform and 30 million EHRs.
They offer fixed-priced quotes and milestone-based payments, aligning incentives with clients.
Their 'All-in-One CRO' solutions cater to specific therapeutic areas like cardiovascular and infectious diseases.
Upsides
Decentralized trials align with Lindus Health's patient-centric approach, enhancing participant reach.
AI integration in trials complements their goal of accelerating clinical trial timelines.
Wearable technology in trials supports continuous monitoring, beneficial for cardiovascular studies.
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