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[Remote] Clinical Project Manager

Remote · United Kingdom Full-time

Note: The job is a remote job and is open to candidates in USA. Alimentiv is seeking a Clinical Project Manager to oversee the planning, execution, monitoring, and delivery of clinical research projects. The role coordinates cross-functional teams, manages timelines, budgets, regulatory compliance, and study deliverables, and serves as a primary contact for sponsors and clients.

Responsibilities

  • Lead the planning, execution, monitoring, and completion of assigned clinical research projects, ensuring project objectives and deliverables are achieved
  • Coordinate cross-functional project teams to ensure activities comply with applicable regulations, industry guidelines, corporate policies, and quality standards
  • Oversee project operations, budgets, regulatory requirements, and patient safety to maintain operational and financial integrity throughout the project life cycle
  • Manage the development, maintenance, and appropriate disposal of essential clinical study documents, data, equipment, and tools, including protocols, SOPs, informed consent forms, and case report forms (CRFs)
  • Assign, track, and oversee interdisciplinary activities, including 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, proactively managing expectations, resolving project-related issues, and maintaining effective communication
  • Organize and facilitate project meetings, prepare investigator updates, and provide regular project progress and status reports to relevant stakeholders
  • Support site and patient recruitment strategies, stakeholder training initiatives, and the development of study-related communication materials
  • Participate in regulatory submissions, audits, third-party vendor selection, and other activities required to support successful project delivery
  • Monitor team performance, project milestones, and deliverable quality to ensure alignment with sponsor expectations, project requirements, and regulatory standards

Skills

  • * Bachelor's degree in a relevant field
  • 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, with the ability to coordinate multiple tasks, track deliverables, and meet project deadlines
  • Strong written and verbal communication skills, with the ability to interact effectively with sponsors, clients, investigators, and cross-functional teams
  • Demonstrated ability to build collaborative working relationships, encourage teamwork, and coordinate interdisciplinary project activities
  • Exceptional attention to detail, with a commitment to maintaining accuracy, compliance, and high-quality project outcomes
  • Self-motivated and results-oriented, with strong problem-solving skills and the ability to proactively identify and address project challenges
  • Commitment to continuous learning, professional development, and adapting to evolving project and organizational requirements
  • Fluency in English, including reading, writing, and speaking
  • Preferably Health Sciences, Clinical Research, or a related discipline

Benefits

  • Home-based opportunity with occasional travel
  • 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
  • Full-time employees become beneficiaries of the Alimentiv Trust after one year of employment, and permanent members after 5 years of employment
  • Optional formal mentorship program (Alimentorship)
  • Country/region annual social events in person
  • Leadership development programs for people leaders in accordance with your seniority
  • Social committee and several other optional initiatives designed to support you in feeling like part of the Alimentiv team

Company Overview

  • Industry-leading specialty GI contract research organization (CRO) transforming clinical trial outcomes and accelerating the development of life-changing therapies. It was founded in 1986, and is headquartered in London, Ontario, CAN, with a workforce of 501-1000 employees. Its website is https://alimentiv.com/.
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