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Parexel

End-to-end clinical trials and regulatory consulting

Event Manager - Meeting Services, Pharmaceutical Congress/Conference

Project ManagementConfirmed live in the last 24 hours
Full-timeLondon, UKNo salary listedRemote

About the Job

Requirements

  • Proven conference and event organization experience in an agency setting.
  • Relevant experience in the pharmaceutical, clinical research, or healthcare industry.
  • Demonstrated ability to manage meetings on time and to a high standard of quality.
  • Strong understanding of international congress logistics.
  • Professional communication skills and a client-focused approach.
  • Strong problem-solving and organizational abilities.
  • Technical expertise with meeting management tools and registration software.
  • Proficiency with Word, Excel, and PowerPoint.
  • Flexible approach and willingness to work in matrix environments.

Responsibilities

  • Lead congress delivery across all operational phases from an agency perspective on behalf of a client.
  • Oversee delegate travel and international meeting logistics.
  • Conduct site visits and manage on-site delivery.
  • Recommend venues and ensure compliance with industry guidelines.
  • Lead project planning and maintain oversight of deliverables.
  • Manage supplier communication and proactively resolve issues.
  • Meet tight deadlines and provide quality control guidance.
  • Manage client expectations and scope changes.
  • Attend and lead client meetings and provide regular status updates.
  • Identify opportunities for follow-on business.
  • Ensure accurate project scoping and budget management.
  • Monitor profitability and financial compliance.
  • Communicate cost implications to management.
  • Maintain expertise in virtual meeting platforms and registration tools.
  • Stay current on industry knowledge, standard operating procedures, and the supplier landscape.
  • Work with minimal supervision and provide cover for the Senior Specialist.

Desired Qualifications

  • A Bachelor's degree is preferred but not essential.

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

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