Idoven is hiring a

Clinical Program Manager

Madrid, Spain
Full-Time
Remote

About us

Idoven is on a mission to prevent heart disease with AI-powered cardiology. With our breakthrough technology to analyze the heart, we help find patients in need of treatment, improve confidence in the accuracy of diagnosis, and get life-saving therapies to patients more quickly and safely.

This is a unique opportunity. With the backing of top-tier global investors, including Insight Partners, Northzone and the European Commision (EIC and Horizon H2020), you'll have the responsibility and resources to shape the creation of a game-changing product that can save millions of lives.

Idoven has been honored with numerous awards, including recognition from UCSF as one of the the best new health applications of AI, CB Insight's top 150 in digital health, the European Seal of Excellence, Best Startup at MEDICA (world's largest medical event), Most Disruptive Startup and Best Health Startup at South Summit, and the Healthy Longevity Catalyst Award from the U.S. National Academy of Medicine.

About you

The Clinical Program Manager is responsible for the design, management, execution of the assigned clinical studies / projects for regulatory submission or evidence generation, in support of the development of artificial intelligence algorithms in the cardiology space to impact the next generation of patient care, to achieve team-level goals.

What will you do

  • Design clinical study protocols with the support of the Team Manager, and develops the project plan in consultation with Idoven clinical team and under the supervision of the Team Manager
  • Ensure the execution of assigned clinical studies with the goal of adhering to target timelines, budget and quality
  • Ensure the clinical studies are audit-ready at all times (e.g. project team training records, central files, system validation, etc.)
  • Medical oversight during trials and functions as SME for scientific and medical questions during the trials
  • Support all investigators and centres involved in multi-centre studies
  • Prepare the documentation required for Ethics Committee approvals under the supervision of the Team Manager
  • Conduct on-site visits to support qualifications, training on implementation and conduct of study protocols
  • Provide oversight of clinical projects to ensure safety concerns and/or adverse events or trends in Field Events Reporting are identified and appropriate responses are developed and executed
  • Be involved in control of device distribution and allocation
  • Evaluate clinical data in preparation of study summary reports for presentations, publications and submissions
  • Engage with Key Opinion Leaders to collect their input as needed for the clinical project

Requirements

What you need to succeed

  • Minimum of 2 years directly supporting clinical research or similar experience in a medical/scientific area
  • Proven expertise in the writing of clinical and non-clinical research protocols including trial design and methodology, and research publications.
  • Experience running multi-centre studies from start to end
  • Proficient knowledge of medical terminology in cardiology
  • Expertise with Good Clinical Practices (GCPs) and regulatory compliance for clinical trials (e.g. applicable ISO Standards, CE Mark)
  • Bachelor’s degree in Statistics, Science, Engineering or related field. Phd is a strong asset.
  • Spanish and English are a must. Other European languages are highly valued.
  • Excellent time management, planning, and organizational skills

Benefits

🚀 Be part of one of the most disruptive startups in HealthTech and AI and make a difference

🏆 Personal and professional growth as part of a fast-growing, international team

🎧No corners cut in having the best tech equipment to do your job

🙋 Flexible remote working environment, where you can choose to work from home and come to our Madrid office whenever you want to

💸 Flexible Remuneration. We give you the flexibility to consume your benefits (from meals, transportation, kindergarten, training) directly from your payroll and receive tax benefits

🧑🏻‍⚕️ Private medical insurance

📚 Training budget

🌴 23 holidays, your birthday off, and December 24th and 31st half days to celebrate!

😎 Regular team events and Thursday happy hours

And much more!

At IDOVEN, we believe in hiring top talented people like you - ambitious, forward thinkers who want to make a difference in the world and have an impact. Apply now via the apply button or contact us via [email protected] .

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