Participant Recruitment Coordinator - FTC

Reposted 13 Days Ago
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Sweden
Junior
Healthtech
The Role
The Participant Recruitment Coordinator manages participant interactions for clinical trials, ensuring a positive experience and data accuracy, while overseeing tracking systems and collaborating with trial teams.
Summary Generated by Built In

🍊Our mission 

We're powering biology's century with radically faster, more reliable clinical trials. Every new treatment needs clinical trials to prove safety and efficacy, but today's infrastructure is stuck in the past- driving up cost, causing delays and ultimately meaning new treatments don’t get to patients. We're fundamentally changing that- not just being a "better CRO," but transforming how people think about developing new treatments, so patients can access breakthrough treatments faster.

Our impact speaks for itself: Since March 2021, we've powered 100+ clinical trials involving tens of thousands of patients. We recently raised a $55M Series B from Balderton Capital, alongside backing from Creandum, Firstminute, Seedcamp, and Visionaries.

🍊What's it like to work here?

When you join us, you’ll experience:

  • High-Impact, Mission-Driven Work: Lindus Health is disrupting an outdated industry, giving you the chance to directly improve patients’ lives and see tangible results from your work.

  • Fast-Paced Growth & Ownership: We recognise hard work and outcomes over anything else. You’ll take on real responsibility, work across different areas, and actively shape the company’s success.

  • Collaborative, No-Ego Culture: Work with smart, driven people in a supportive and informal environment. At Lindus we break down silos, fun is a core value, and creativity is encouraged.

Ready to power biology's century? We'd love to hear from you.

🍊About the role 

We’re looking for a Swedish speaking Participant Recruitment Coordinator to join our Clinical Operations team on a Fixed Term Contract to support the growth of our team and manage the participant interactions of our trials.  

🍊About you 

We'd like to hear from you if...

  • You have experience in utilising various tech tools; bonus if these include Calendly, Docusign, Medi2data, Dial Pad, Florence and Sealed Envelope 

  • You have experience in patient onboarding and set up; including running screening calls and patient follow up 

  • You have experience of maintaining a tracking system and executing follow-up procedures 

  • You have high agency and a bias for action and are able to adhere to protocol timelines and able to be flexible in response to work priorities and issues 

  • You are passionate and curious about our mission; changing how the healthcare industry operates and how new health treatments are developed 

  • You want to learn what life is like at a high-growth, mission-driven VC funded startup 

You belong here! If your experience and interests match with some of the above, we want you to apply.

🍊What you’ll focus on
  • Conduct all participant facing tasks, ensuring a positive trial experience and excellent data accuracy within our platform, Citrus

  • Oversee data collection and in-person processes (e.g. MRI scans) are conducted smoothly

  • Maintain and update participant trackers and Investigator Site File (ISF)

  • Assist PI with day-to-day trial implementation and respond to CRO queries

  • Respond to any CRO data queries

  • Escalate safety, data integrity or trial operational issues to the TL/CRO team

  • Reporting AEs and SAEs

  • Collaborate effectively with trial teams to ensure seamless participant experiences throughout the trial journey

  • Contribute to team discussions by sharing participant feedback and suggesting process improvements

  • Cross Functional working with Clin Ops - keeping TL and STM  updated at all times and other PRCs aware of trial status

🍊What we offer (EU)
  • 20 days holiday allowance per annum (pro rata’d to length of contract)

  • Enhanced Parental Leave - 16 weeks at full pay for primary caregivers and 6 weeks at full pay for secondary caregivers (at 1 year of employment)

  • Please note you will not be required to join company off sites or company wide meetings in this role.

🍊Our hiring process
  • We believe hiring should be transparent, respectful of your time, and give you a real feel for what Lindus Health is like. Here's what to expect:

    • Online Logical Reasoning and Problem Solving test (20 minutes)

    • Initial conversation with Sarah, our ClinOps Talent Partner (20 minutes)

      Get to know each other, discuss the role, and answer any questions about Lindus

    • Technical/functional interview with two members of our Clinical Operations team (45 minutes)

      This will include a task you’ll need to prepare in advance of the interview and talk to

    • Values interview with 2 team members of leadership (30 minutes)

      A chance to get to know each other and explore how our values align

We will only contact you from lindushealth.com email addresses. Please check the spelling of emails which appear to come from Lindus Health carefully before responding. We will never ask for your financial information over email.
We are an equal opportunity employer committed to building a diverse and inclusive workforce. We evaluate all candidates based solely on their skills, experience, and qualifications relevant to the role. We do not discriminate on the basis of race, ethnicity, religion, gender, gender identity, sexual orientation, age, disability, veteran status, or any other legally protected status

Top Skills

Calendly
Citrus
Dial Pad
Docusign
Florence
Medi2Data
Sealed Envelope
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The Company
HQ: London
109 Employees

What We Do

Lindus Health is an anti-CRO running radically faster, more reliable clinical trials for life science pioneers.

We do this thanks to a commercial model that aligns incentives (fixed-price quotes per study, with milestone-based payments), marrying a world-class clinical operations team with our unique software platform, and access to 30 million Electronic Health Records. We handle the end-to-end execution of clinical studies, including design, patient recruitment, clinical data capture, monitoring and project management.

We have helped over 100 sponsors run entire clinical studies across the US, UK, and Europe up to 2x faster than traditional CROs

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