Clinical Project Manager – Contract

🔥 13 hours ago

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥 Clinical Operations

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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ProTrials Research Inc.

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 1996

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

ProTrials Research Inc. is a clinical research organization (CRO) headquartered in the United States, offering a wide range of services to the pharmaceutical, biotechnology, and medical device industries. The company provides quality-driven site management, clinical monitoring, project management, data management, and supportive clinical development services. With a focus on therapeutic areas such as oncology, ophthalmology, central nervous system, infectious diseases, women's health, and medical devices & diagnostics, ProTrials is dedicated to delivering high-quality clinical research. Their services include project management, clinical operations, quality assurance, medical and regulatory support, and they also act as a functional service provider, emphasizing virtual trials and remote monitoring capabilities.

📋 Description

• Lead all clinical study operations, including strategic/tactical planning, organization, and direction of study projects • Oversee clinical project timelines, reports, budgets, monitoring, site and vendor management, clinical supplies, and data collection • Facilitate communication between sponsor, study team, and functional groups • Manage, motivate, mentor, and delegate responsibilities to study team members • Provide financial oversight of study budgets, including out-of-scope tracking • Collaborate with senior management on study updates, progress, resourcing, sponsor issues, and health status • Develop, maintain, and distribute project plans throughout the study lifecycle • Manage studies in compliance with GCP, SOPs, regulatory requirements, and project-specific plans • Assess resourcing and training needs and implement training plans • Track study risks, escalate issues, and adjust timelines as needed • Oversee outside vendor activities and deliverables

🎯 Requirements

• RN or Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training and previous CRA experience • Outstanding interpersonal, oral, and written communication skills • Proven effectiveness as a team leader • Prior experience successfully managing multifaceted studies from inception through implementation and completion • Outstanding organizational and time management skills • Experience managing projects in a virtual environment • Demonstrated ability to lead by example and encourage team members to seek solutions independently • Proficiency in Microsoft Word, Excel, and PowerPoint are required • Experience with MS Project and OneNote a plus