Associate Clinical Research Medical Director CRM

Role Summary

Associate Clinical Research Medical Director CRM — Remote.

Responsibilities

• Accountable for all country clinical/medical aspects associated with Development and prioritized research programs/trials by providing clinical strategic and tactical leadership as the Country Clinical Development representative.
• Gathers, informs, and acts on clinical/medical/scientific insights for clinical trial concept sheets/protocols, Informed Consent Forms (ICFs) and other relevant clinical documents to optimize clinical trial implementation.
• Drives the identification and involvement of qualified investigators with greatest recruitment potential, identifies clinical recruitment hurdles and drives clinical recruitment activities to overcome these hurdles.
• Accountable for adherence to safety standards and clinical data quality in the country by providing general clinical/medical support for trial related safety findings.
• In close collaboration with other country functions (e.g., clinical trial operations, Medical Affairs and Patient Engagement) actively contributes to successful allocation, fast clinical trial start-up, timely recruitment, early identification of potential delays, and development and implementation of mitigation plans.

Qualifications

• Advanced degrees required; M.D., M.D. equivalent, Ph.D., or Pharm.D.
• Cardiology Subspecialty or Cardiovascular clinical trial experience preferred
• Ability to manage a study from the scientific/medical/clinical perspective, and a demonstrated capability to problem solve and mediate complex scientific/clinical/medical/operational issues.
• Ability to lead effectively by communicating well, motivating a cross- functional team, and handling and delegating responsibilities.
• Agility to move quickly across different therapeutic areas and indications.
• Demonstrated problem-solving skills and comfort with complexity.
• Ability to prepare and deliver high quality presentations.
• Ability to travel up to 30%
• Ideally, 3 years of clinical development experience in the pharmaceutical industry or clinical practice.
• Sound understanding of the overall clinical development process, and ICH/GCP principles.

Skills

• Clinical development planning
• Site start-up execution
• Investigator engagement and recruitment strategy
• Regulatory and safety knowledge
• Cross-functional leadership and collaboration
• Scientific/medical communication and training

Education

• Advanced degrees required; M.D., M.D. equivalent, Ph.D., or Pharm.D.