Clinical Lead, Healthcare

Role Description

Piper Companies is seeking a Clinical Lead to join an innovative organization within the clinical research and biotechnology industry for a fully remote, permanent opportunity. The Clinical Lead will provide operational leadership for regional clinical trial activities, partnering with project teams and study stakeholders to ensure successful execution of study start-up, site management, regulatory oversight, and monitoring activities across multiple locations.

• Oversee site feasibility assessments, site identification efforts, and site selection activities for regional and global clinical studies.
• Coordinate ethics committee and regulatory submission activities, ensuring documentation is complete and approvals are obtained within required timelines.
• Partner with project leadership to manage investigational product logistics, including import/export documentation, permits, and distribution planning.
• Lead clinical research associate (CRA) meetings, provide ongoing study oversight, and support communication of key project updates and action items.
• Serve as a primary point of contact for sponsors and internal stakeholders, delivering study progress updates and helping resolve operational challenges.

• Extensive experience conducting advanced clinical monitoring and site management activities across multiple study locations.
• Demonstrated leadership experience with the ability to coach, mentor, and support clinical operations teams.
• Strong knowledge of clinical trial processes, regulatory requirements, and site management best practices.
• Excellent organizational, communication, and stakeholder management skills in a fast-paced environment.
• Bachelor's degree in Life Sciences, Nursing, or a related field preferred.

Salary Range: $145,000-$165,000/year (USD) + 8% on target annual bonus

Comprehensive Benefits:
Medical, Dental, Vision, sick leave if required by law, and 401K

clinical research, clinical trials, clinical lead, clinical operations, site management, clinical monitoring, regulatory submissions, ethics committee submissions, feasibility studies, study start-up, investigational product management, project management, CRO, GCP, ICH guidelines, sponsor communication, CRA leadership, biotechnology, life sciences, clinical development, regulatory compliance, stakeholder management, risk management, protocol adherence, study oversight, monitoring activities, clinical study execution, site activation, data quality, operational leadership, drug development, global studies, regional studies, clinical research associate, trial management, communication skills, mentoring, coaching, healthcare research.

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