Participant Recruitment Coordinator - FTC

Germany

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Not SpecifiedCompensation

Entry Level & New GradExperience Level

Part TimeJob Type

UnknownVisa

Biotechnology, Healthcare, PharmaceuticalsIndustries

Requirements

Candidates should have experience utilizing various tech tools such as Calendly, Docusign, Medi2data, Dial Pad, Florence, and Sealed Envelope. Experience in patient onboarding and setup, including running screening calls and patient follow-up, is required. Proven experience in maintaining a tracking system and executing follow-up procedures is necessary. The ideal candidate will possess high agency, a bias for action, and the ability to adhere to protocol timelines while remaining flexible. Fluency in German is also a requirement for this role.

Responsibilities

The Participant Recruitment Coordinator will conduct all participant-facing tasks to ensure a positive trial experience and excellent data accuracy within the Citrus platform. This role involves overseeing data collection and in-person processes like MRI scans, maintaining and updating participant trackers and the Investigator Site File (ISF), and assisting the Principal Investigator (PI) with daily trial implementation. Responsibilities also include responding to CRO queries and data queries, escalating safety, data integrity, or operational issues to the appropriate teams, and reporting Adverse Events (AEs) and Serious Adverse Events (SAEs). The coordinator will collaborate with trial teams for seamless participant experiences, contribute to team discussions by sharing participant feedback, and suggest process improvements. They will also engage in cross-functional work with Clinical Operations, keeping the Trial Lead (TL) and Study Team Manager (STM) updated, and informing other Participant Recruitment Coordinators (PRCs) of trial status.

Skills

Participant Recruitment

Clinical Trials

Patient Onboarding

Calendly

Docusign

Medi2data

Dial Pad

Florence

Sealed Envelope

German Language

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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