Clinical Project Manager

Jobgether

1d • $110,000 - $135,000 • Remote

About The Position

This role provides an opportunity to lead and manage complex clinical trials, ensuring timely and high-quality delivery while supporting patient-centered research. The Clinical Project Manager will oversee all operational aspects of assigned studies, from start-up to close-out, coordinating cross-functional teams, vendors, and stakeholders. You will manage project timelines, budgets, and resources, ensuring compliance with regulatory standards and organizational SOPs. The position requires strong communication, leadership, and problem-solving skills, as well as the ability to work independently in a semi-remote, distributed environment. Travel will be required up to 30% to support study activities and site engagement. This role offers exposure to innovative virtual and decentralized clinical trial models, providing a chance to make a meaningful impact on patient access and study outcomes.

Requirements

• Undergraduate degree in a health-related field or equivalent combination of education, training, and experience.
• 5+ years of experience in clinical research and project management, with knowledge of trial conduct, virtual/DCT trial experience preferred.
• Expertise in clinical trial management systems (CTMS) and relevant regulatory guidelines (ICH GCP).
• Strong communication, collaboration, and interpersonal skills.
• Ability to manage complex projects independently, adapt to change, and work across multiple time zones.
• Strong analytical and critical thinking skills with proactive problem-solving abilities.

Nice To Haves

• Experience in CRO, site management organization (SMO), or sponsor settings is preferred.

Responsibilities

• Lead cross-functional project teams and vendors to deliver clinical trials successfully.
• Oversee study start-up, enrollment, execution, and close-out activities.
• Serve as the primary liaison with clients, ensuring expectations, deliverables, and communication are effectively managed.
• Prepare and deliver project updates, dashboards, and reports on recruitment, KPIs, risks, protocol deviations, and other study metrics.
• Manage project resources, including forecasting, assigning tasks, approving hours, and monitoring efficiency against budget.
• Support operational plans, vendor management, site contracts, and compliance with regulatory and SOP requirements.
• Identify risks and mitigation strategies, escalate issues as needed, and document lessons learned for continuous improvement.

Benefits

• Competitive base salary ($110,000 – $135,000, annualized, depending on experience).
• Top-tier healthcare coverage including medical, dental, and vision.
• 100% 401(k) match for up to 4% of contributions with immediate vesting.
• Flexible remote work arrangements with distributed team model.
• Company-provided laptop (PC or Mac) and monthly stipend for internet and phone.
• Short- and long-term disability, life insurance, and additional wellness benefits.
• Opportunities to contribute to inclusive, patient-centered clinical research and grow in a collaborative, innovative environment.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level