Clinical Program Manager

hace 4 semanas


Madrid, Madrid, España Idoven A tiempo completo
About Us

At Idoven, we're revolutionizing cardiology with AI-powered technology. Our mission is to prevent heart disease by analyzing the heart and providing life-saving therapies to patients more quickly and safely.

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

Idoven has been recognized for its excellence, receiving awards from UCSF, CB Insights, the European Seal of Excellence, and the Healthy Longevity Catalyst Award from the U.S. National Academy of Medicine.

About You

We're seeking a Clinical Program Manager to design, manage, and execute clinical studies and projects for regulatory submission or evidence generation. This role will support the development of artificial intelligence algorithms in cardiology to impact patient care.

Key Responsibilities:

  • Design clinical study protocols and develop project plans in consultation with the Idoven clinical team.
  • Ensure the execution of assigned clinical studies, adhering to target timelines, budget, and quality.
  • Provide medical oversight during trials and serve as a subject matter expert for scientific and medical questions.
  • Support investigators and centers involved in multi-center studies.
  • Prepare documentation for Ethics Committee approvals.
  • Conduct on-site visits to support qualifications, training, and implementation of study protocols.
  • Provide oversight of clinical projects to ensure safety concerns and adverse events are identified and addressed.
  • Control device distribution and allocation.
  • Evaluate clinical data for study summary reports.
  • Engage with Key Opinion Leaders for input on clinical projects.
Requirements

To succeed in this role, you'll need:

  • Minimum 2 years of experience directly supporting clinical research or a similar medical/scientific area.
  • Proven expertise in writing clinical and non-clinical research protocols, including trial design and methodology.
  • Experience running multi-center studies from start to end.
  • Proficient knowledge of medical terminology in cardiology.
  • Expertise in Good Clinical Practices (GCPs) and regulatory compliance for clinical trials.
  • Bachelor's degree in Statistics, Science, Engineering, or a related field. A 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

As a member of our team, you'll enjoy:

  • Personal and professional growth in a fast-growing, international environment.
  • The best tech equipment to do your job.
  • A flexible remote working environment.
  • Flexible remuneration with tax benefits.
  • Private medical insurance.
  • A training budget.
  • 23 holidays, your birthday off, and December 24th and 31st half days.
  • Regular team events and Thursday happy hours.


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