Clinical Project Manager (US)

Alimentiv

$95K — $159K *
US-AnywhereRemote in Raleigh, NC
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Health Sciences or Clinical Research.
  • 1-3 years of experience in clinical study management.
  • Strong communication skills and self-motivation.
  • Attention to detail with a focus on collaborative relationships.
  • Commitment to continuous learning and team building.
  • Fluent in English (reading, writing, speaking).

Responsibilities

  • Manage all stages of clinical research projects from planning to completion.
  • Ensure compliance with regulations and corporate policies through collaboration with experts.
  • Maintain operational, financial, and regulatory integrity.
  • Develop training materials and handle regulatory submissions as needed.
  • Oversee data, documents, and tools related to project management.
  • Prepare project reports and investigator updates throughout the project life cycle.
  • Act as the primary client/sponsor liaison, managing expectations and queries.

Benefits

  • Home-based working conditions for flexibility.
  • Occasional travel for on-site engagements.
Full Job Description
Project Management

  • Manage the planning, execution, progress and completion of assigned clinical research projects.
  • Work with functional experts to ensure all project activities comply with applicable regulations, guidelines, and corporate policies.
  • Maintain operational, financial and regulatory integrity and safety.
  • Develop and/or participate in the development of project communications, training, regulatory submissions and/or audits and selection of third party vendors as required.


Documents and Tools

  • Manage a cross-functional team to ensure the appropriate creation, delivery, maintenance and disposal of all related data, documents, equipment and tools, including protocols, SOPs, informed consent forms, case report forms and instructions.
  • Prepare investigator updates and other project related reports as required to support the proper conduct and execution throughout the life cycle of assigned projects.


Project Team Performance

  • Identify, assign and monitor the completion of interdisciplinary project tasks that include site monitoring, CRF and database development and revision, data collection, patient safety/adverse event management, document management, statistical analysis and/or final report writing and publications.
  • Ensure task completion performance meets or exceeds quality standards and sponsor/client, project and regulatory expectations and guidelines.


Client/Sponsor Support

  • Act as primary liaison throughout the project life cycle ensuring client/sponsor expectations are appropriately managed by addressing and resolving queries/issues, planning and executing all project meetings, assisting with site and patient recruitment strategies and materials, assisting with the development of stakeholder training and by regularly providing sponsor/client with project status and update reports.


Qualifications

  • Applicants should have a minimum of a Bachelor's Degree in a relevant field of study (Health Sciences, Clinical Research preferred) and 1-3 years of experience in clinical study management
  • The successful candidate must exhibit the following skills: self-motivation with strong communication skills and a commitment to achieving positive results.
  • Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results.
  • Ability to engage in continuous learning and self-development.
  • Ability to continually foster teamwork.
  • Fluent in reading, writing, and speaking of English


Working Conditions

  • Home Based
  • Occasional travel


$95,500 - $159,000 a year

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