Remote Senior Clinical Project Manager — Global Trials Leader

Zachary Piper Solutions; United States; Remote; USD 160,000 - 175,000; Full time

Benefits offered by this job

Health benefits

Vision benefits

Dental benefits

PTO & Paid holidays

Job summary

Piper Companies is seeking a Senior Clinical Project Manager to support a growing biotechnology and clinical research organization. The role is fully remote and ideal for an experienced clinical operations leader with a track record managing global clinical trials across multiple therapeutic areas.

Responsibilities include directing Phase I–IV trials, liaising with sponsors and CROs, and overseeing timelines, budgets, and study milestones.

Qualifications

• 8+ years of clinical project management experience.
• Experience across Cardiovascular, MASH, Hepatology, Obesity and Dermatology.
• Strong knowledge of ICH-GCP guidelines and FDA regulations.
• Experience managing CROs, vendors, budgets, timelines, and multinational studies.
• Bachelor's degree required; advanced degree preferred.

Responsibilities

• Direct the planning, execution, and oversight of Phase I-IV clinical trials.
• Serve as the liaison between sponsors, CROs, sites, vendors and stakeholders to drive study objectives.
• Monitor trial progress, identify operational risks and implement mitigation strategies.
• Oversee study timelines, enrollment metrics, vendor activities, and financial tracking.
• Lead cross-functional study teams through protocol implementation, database lock, and closeout.

Skills

Clinical PM

ICH-GCP knowledge

Budget management

Vendor management

Education

Bachelor's degree in Life Sciences or related field

Advanced degree preferred (MS/PhD)

Job description

Piper Companies is seeking a Senior Clinical Project Manager to support a growing biotechnology and clinical research organization. The role is fully remote and ideal for an experienced clinical operations leader with a track record managing global clinical trials across multiple therapeutic areas.

Responsibilities include directing Phase I–IV trials, liaising with sponsors and CROs, and overseeing timelines, budgets, and study milestones.