Remote Clinical Project Manager — Lead Global Trials

Pharmavise Corporation; United States; Remote; USD 110,000 - 150,000; Full time

Benefits offered by this job

Paid holidays

Paid Time Off (PTO)

Medical insurance

Healthy work-life balance

Job summary

Pharmavise Consulting Corporation seeks a Clinical Project Manager to lead and manage all aspects of clinical trials remotely in the U.S. You will ensure compliance with GCP/ICH, timelines, budgets, and SOPs while coordinating cross-functional teams, sites, CROs, and sponsors.

The role requires 5+ years in clinical research with 2+ years in project management, strong communication skills, and proficiency with CTMS, MS Project, and MS Office.

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field (Master’s or PMP certification a plus).
• Minimum of 5 years of experience in clinical research, including 2+ years in a project management role.
• Proven ability to manage multi-site and/or global studies across various phases (Phase I–IV).
• Strong understanding of GCP, ICH guidelines, and clinical trial regulatory requirements.

Responsibilities

• Develop, manage, and oversee clinical trial project plans including timelines, milestones, budgets, and resource allocation.
• Serve as the primary liaison between internal teams, clinical research sites, CROs, vendors, and external partners.
• Lead cross-functional team meetings and coordinate study activities such as site selection, study start-up, monitoring, and close-out.
• Ensure adherence to GCP, ICH guidelines, regulatory standards, and company SOPs throughout study conduct.
• Monitor progress against timelines and budget; proactively identify risks and implement mitigation strategies.
• Oversee vendor performance and manage contract deliverables for CROs, central labs, data management providers, etc.
• Track clinical trial metrics and prepare regular status reports for internal leadership and/or sponsors.
• Support regulatory and audit readiness, including contributing to study documentation and inspection preparation.
• Participate in protocol development, CRF design, and review of key trial documents (e.g., ICF, SAP, CSR).

Skills

Project management

Leadership

Communication

GCP/ICH knowledge

Education

Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field

PMP certification (plus)

Tools

CTMS

MS Project

Microsoft Office Suite

Job description

Pharmavise Consulting Corporation seeks a Clinical Project Manager to lead and manage all aspects of clinical trials remotely in the U.S. You will ensure compliance with GCP/ICH, timelines, budgets, and SOPs while coordinating cross-functional teams, sites, CROs, and sponsors.

The role requires 5+ years in clinical research with 2+ years in project management, strong communication skills, and proficiency with CTMS, MS Project, and MS Office.