Inactive
A

Alimentiv

Runs clinical trials for digestive disease treatments

Director: Clinical Study Management - Project Management

Clinical Research OperationsPosted on Nov 2
Full-timeNo salary listed

About the Job

Requirements

  • An undergraduate university degree (Bachelor or Honors Bachelor) and at least 10 years of related experience and training or continuous ongoing development, or a college diploma/degree and at least 15 years of related experience.
  • Deep experience in the contract research organization industry with full-service project management leadership, coaching and leading a team.
  • Phase II experience is required.
  • Significant financial resource management experience, including participation in budget setting, autonomous expenditure or revenue-generation decisions within company policy, or financial processing, reconciliation and reporting.

Responsibilities

  • Provide leadership and oversight for global activities and timelines related to full-service clinical trial execution, including oversight of project management and project finance teams.
  • Participate in developing and implementing organizational strategies, technologies and best practices for customer service, staff development, quality information management reporting, and divisional goals.
  • Develop and improve policies and processes; oversee product quality, compliance monitoring, staff resource planning, and staff and contractor performance management.
  • Represent project and finance teams to sponsors and clients throughout the project life cycle.
  • Ensure team members deliver high-quality, timely service and maintain service delivery processes in accordance with corporate and industry best practices and regulatory requirements and guidelines.
  • Support Business Development by assisting with bid development and defense as required.
  • Participate in operational planning and advocate for the functional area and its stakeholders.
  • Guide departmental planning and implementation, translating strategic plans into measurable short- and long-term operational goals and targets.
  • Oversee or participate in project development with sponsors and functional directors to negotiate and deliver quality products; assess resource, financial and safety requirements; assign resources; oversee trial conduct and information and data confidentiality; and help project teams troubleshoot and resolve issues while aligning work with corporate objectives.
  • Ensure sufficient project-level staffing and maintain utilization targets.
  • Represent project operations on cross-department planning initiatives.
  • Ensure functional areas are adequately staffed with qualified personnel and support managers and leaders with work allocation, resource planning, staff allocation, training and development, employee engagement, team development, and performance management, including staff evaluation, performance improvement and lost-time management.
  • Represent the project operations team at client meetings.
  • Represent project operations at business development meetings, including bid defenses, general capabilities discussions and scientific conferences.
  • Attend and present at investigator meetings as needed.
  • Collaborate with the leadership team to improve project services, minimize organizational risk, meet regulatory and industry standards, and promote programs that support organizational growth in clinical research and research services.
  • Plan, manage, advocate and report for the department during budget and annual operational review processes, in conjunction with the senior leadership team.
  • Maintain knowledge of financial and regulatory risks and requirements related to department service delivery and direct development of methods to review, monitor and manage them.
  • Work with Business Development to prepare budgets and proposal text for requests for proposal, requests for information and statements of work.
  • Oversee change order development for full-service projects and ensure project costs are realized in line with work performed.

Desired Qualifications

  • Phase III experience is highly desirable.
  • Experience in gastrointestinal clinical trial project management is highly desirable.

About the Company

Alimentiv

Runs clinical trials for digestive disease treatments

Alimentiv runs clinical trials for pharmaceutical and biotechnology companies developing treatments for gastrointestinal diseases. Its contract research services cover study design, site monitoring and regulatory submissions, with medical imaging used to measure how patients respond to treatment. The company combines central image reading with tissue analysis and biomarker testing through sister laboratory AcelaBio. Sponsors pay for trial execution, scientific consulting and statistical services that support drug development from early studies through regulatory review. Founded in 1986, Alimentiv is headquartered in London, Ontario, and operates internationally.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
London, Canada
Founded
1986

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