Clinical Project Manager

🔥 0 minutes ago

🌐 United States, Canada – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote

🌲 North Carolina, Ohio, +2 more states – Remote

🌲 North Carolina – Remote 🏈 Ohio – Remote 🔔 Pennsylvania – Remote 🤠 Texas – Remote

💵 $95.5k - $159k / year

⏰ Full Time

🟢 Junior

🏥 Clinical Operations

👻 Ghost score 1%

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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Alimentiv

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2020

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Alimentiv is a specialty contract research organization focused on gastrointestinal (GI) and liver diseases. With over 30 years of experience, Alimentiv offers a comprehensive range of clinical research and imaging services, including clinical trial management, site management, regulatory affairs, and precision medicine. The company is at the forefront of medical research and development, providing state-of-the-art imaging solutions and actionable biomarker insights. Alimentiv supports the development of GI compounds and is active in more than 60 countries, working with a network of medical and operational experts to accelerate clinical trials and patient recruitment.

📋 Description

• Lead the planning, execution, monitoring, and completion of assigned clinical research projects • Coordinate cross-functional project teams and ensure compliance with regulations, industry guidelines, corporate policies, and quality standards • Oversee project operations, budgets, regulatory requirements, and patient safety • Manage essential clinical study documents, data, equipment, and tools, including protocols, SOPs, informed consent forms, and CRFs • Assign, track, and oversee site monitoring, database development, data collection, adverse event management, statistical analysis, and clinical study reporting • Serve as the primary point of contact for sponsors and clients • Manage expectations, resolve project-related issues, and maintain effective communication • Organize and facilitate project meetings, prepare investigator updates, and provide project progress and status reports • Support site and patient recruitment strategies, stakeholder training, and study-related communication materials • Participate in regulatory submissions, audits, and third-party vendor selection • Monitor team performance, project milestones, and deliverable quality

🎯 Requirements

• Bachelor's degree in a relevant field, preferably Health Sciences, Clinical Research, or a related discipline • 1–3 years of experience in clinical study management, with exposure to clinical research project coordination and execution • Strong understanding of clinical research processes, regulatory requirements, quality standards, and study documentation practices • Excellent project management and organizational skills • Ability to coordinate multiple tasks, track deliverables, and meet project deadlines • Strong written and verbal communication skills • Ability to interact effectively with sponsors, clients, investigators, and cross-functional teams • Ability to build collaborative working relationships and coordinate interdisciplinary project activities • Exceptional attention to detail and commitment to accuracy, compliance, and high-quality outcomes • Strong problem-solving skills and ability to proactively identify and address project challenges • Commitment to continuous learning, professional development, and adapting to evolving requirements • Fluency in English, including reading, writing, and speaking • Ability to work in a home-based environment and travel occasionally as required • Resumes must be submitted in English

🏖️ Benefits

• Performance-Based Incentive Program / Short-Term Incentive Plan (STIP) • Education Reimbursement program for full-time employees • Monthly Cell Phone and Remote Work Allowance (dependent on role eligibility) • One time office setup allowance • Working while visiting program – up to 4 weeks per year • Flexible Summer Hours Program from May – September • Employee referral incentive • Alimentiv Trust benefits after one year of employment, with permanent membership after 5 years • Optional formal mentorship program (Alimentorship) • Country/region annual social events in person • Leadership development programs for people leaders • Social committee and other optional initiatives • Additional benefits may be available depending on the country of employment and local policies and eligibility