Remote Clinical Trial Project Lead | CRO

HRCRS

United States

Hybrid

USD 90.000 - 130.000

Vollzeit

vor 23 Stunden
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Heart Rhythm Clinical Research Solutions is seeking a Project Manager to lead the planning, coordination, and execution of clinical trials. You will act as the main liaison for sponsors, investigators, and stakeholders, ensuring trials progress on plan and meet regulatory standards.

The role requires 5+ years in clinical project management within CRO/biotech/pharma, strong communication, and solid PM software proficiency. Remote work with some travel may be needed across the United States.

Qualifikationen

  • Bachelor’s degree in a life science or related field; master’s preferred or relevant experience considered.
  • Minimum 5 years of clinical project management in CRO/biotech/pharma.
  • Strong understanding of clinical trials planning, execution and regulatory requirements.
  • Excellent communication and interpersonal skills; capable of managing multiple projects.

Aufgaben

  • Plan, coordinate, and oversee all stages of clinical trials from planning to closeout.
  • Ensure trials comply with protocol, SOPs, GCP, and regulatory requirements.
  • Serve as primary sponsor/investigator liaison and provide timely project updates.
  • Identify risks and implement mitigation strategies.
  • Collaborate with internal teams and vendors to meet project goals.
  • Oversee data management ensuring data integrity.

Kenntnisse

Project management
Communication
Problem solving
Stakeholder management
Regulatory understanding

Ausbildung

Bachelor’s degree in life science
Master’s degree or certification preferred

Tools

PM software

Jobbeschreibung

Heart Rhythm Clinical Research Solutions is seeking a Project Manager to lead the planning, coordination, and execution of clinical trials. You will act as the main liaison for sponsors, investigators, and stakeholders, ensuring trials progress on plan and meet regulatory standards.

The role requires 5+ years in clinical project management within CRO/biotech/pharma, strong communication, and solid PM software proficiency. Remote work with some travel may be needed across the United States.

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