P

Parexel

End-to-end clinical trials and regulatory consulting

Senior Project Manager

Project ManagementConfirmed live in the last 24 hours
Full-timeNo salary listedRemote

About the Job

Requirements

  • Problem-solving ability.
  • Project leadership and management knowledge.
  • Strong interpersonal and cross-cultural communication skills.
  • A client-focused approach.
  • Teamwork and collaboration skills.
  • Ability to communicate in English.
  • Project management experience.

Responsibilities

  • Serve as the client contact, confirm statements of work, budgets, requirements, and expectations, and understand the project scope and requirements.
  • As needed, arrange and facilitate client meetings to discuss needs and issues related to regulatory services and develop strategic plans.
  • Manage timelines, costs, and staffing throughout the project lifecycle, from team formation through project completion.
  • Collect information from consultants and manage schedule and resource changes.
  • Set up required systems and tools and time codes in accordance with standard operating procedures and project management plans.
  • Coordinate and attend PMDA consultations.
  • Arrange and manage training.
  • Prepare for project meetings.
  • Liaise with vendors, including interpreters, and provide the necessary files.
  • Improve project efficiency and performance.
  • Prepare, analyze, and review budget management reports.

Desired Qualifications

  • Experience in the pharmaceutical industry is preferred.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

Recently Posted Jobs

Explore more opportunities at Parexel

See more jobs