Cardiovascular Clinical Development Director

ClinLab Solutions Group

Massachusetts

On-site

USD 250,000 - 400,000

Full time

36 hours ago
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Job summary

ClinLab Solutions Group in Suffolk County, MA, is seeking a physician leader to head cardiovascular clinical development. You will drive strategy, trial design, regulatory engagement, and cross-functional execution to advance cardiovascular programs.

The role requires an MD/DO with cardiology board eligibility, 10+ years in clinical research, and a proven record of leading multi-phase programs across regions, with strong GCP/ICH knowledge and authority interactions.

Qualifications

  • MD or DO with board certification in Cardiology.
  • 10+ years in clinical research and drug development.
  • Proven ability to design and run multi-phase programs across regions.
  • Strong knowledge of GCP, ICH, global regulatory requirements.
  • Experience leading cross-functional teams and engaging with regulators.
  • Excellent analytical, strategic, and communication skills.
  • Experience authoring clinical and regulatory documents and submissions.

Responsibilities

  • Develop and implement long-term cardiovascular clinical development strategies.
  • Lead design, execution, and oversight of clinical trials across phases.
  • Provide medical leadership and scientific guidance to cross-functional teams.
  • Oversee safety data assessment and risk mitigation with pharmacovigilance.
  • Contribute to regulatory submissions and health authority interactions.
  • Collaborate with R&D, clinical operations, biostatistics, regulatory affairs, and commercial.
  • Engage with investigators and key opinion leaders to inform program direction.
  • Stay current on scientific advances and therapeutic area trends.

Skills

Leadership
Regulatory experience
Cross-functional leadership
Strategy
Communication

Education

MD or DO

Job description

ClinLab Solutions Group in Suffolk County, MA, is seeking a physician leader to head cardiovascular clinical development. You will drive strategy, trial design, regulatory engagement, and cross-functional execution to advance cardiovascular programs.

The role requires an MD/DO with cardiology board eligibility, 10+ years in clinical research, and a proven record of leading multi-phase programs across regions, with strong GCP/ICH knowledge and authority interactions.

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