Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
ICON plc

Project Manager, Laboratory

ICON plc

. Coordinate project and programme management delivery .

Posted 10/9/2026full-timeRemote • MexicoMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in project management within clinical research, ensuring compliance with Good Clinical Practice while effectively communicating with sponsors and managing multiple studies. Capable of analyzing clinical trials and interpreting complex medical data to support innovative treatments.

Highest-signal resume keywords
Project ManagementGood Clinical PracticeClinical Trial DesignCommunication SkillsOrganizational Skills

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Project ManagementClinical Trial DesignData AnalysisRegulatory ComplianceStudy Documentation Management
Soft Skills
Interpersonal SkillsDetail-OrientedProfessional Communication
Industry Keywords
Clinical ResearchLife SciencesHealthcareSponsor MeetingsStudy Management

About the role

Key responsibilities & impact
  • Coordinate project and programme management delivery
  • Resolve issues and develop team capability
  • Act as the Sponsor's main contact person regarding ICON services, including day-to-day management of studies
  • Attend and represent ICON at Sponsor meetings
  • Manage 10-15 studies in accordance with Good Clinical Practice
  • Communicate study progress to Sponsors in a responsible and professional manner
  • Provide Sponsors with regular management reports
  • Provide ICOLAB support to sponsor personnel
  • Design and analyse clinical trials, interpret complex medical data, and contribute to innovative treatments and therapies

Requirements

What you’ll need
  • Bachelor's degree in a relevant field such as life sciences or healthcare
  • Previous experience in project management within a laboratory or clinical research setting
  • Strong communication and interpersonal skills, with the ability to represent the company at sponsor meetings
  • Ability to manage multiple studies concurrently while ensuring adherence to regulatory standards and guidelines
  • Detail-oriented with strong organizational skills to effectively manage study documentation and timelines
  • Legal right to work in the country where the role is based

Benefits

Comp & perks
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways