Clinical Project Manager (US)

Alimentiv

$95K — $159K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Health Sciences or Clinical Research preferred
  • 1-3 years experience in clinical study management
  • Strong communication skills and self-motivation
  • Attention to detail and relationship-building skills
  • Commitment to continuous learning and teamwork
  • Fluent in English (reading, writing, speaking)

Responsibilities

  • Manage planning, execution, and completion of clinical research projects
  • Ensure project activities comply with regulations and corporate policies
  • Maintain operational, financial, and regulatory integrity
  • Develop project communications, training, and regulatory submissions
  • Manage cross-functional team for document and data management
  • Prepare project-related reports and investigator updates
  • Act as primary liaison for client/sponsor communication and support

Benefits

  • Home-based working conditions
  • Opportunities for occasional travel
  • Accommodations for applicants with disabilities available
  • Support for continuous learning and professional development
  • Utilization of AI tools in the hiring process for efficiency
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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