Remote Lab Project Manager - Clinical Trials

ICON Strategic Solutions; Mexico; On-site; PHP 1,058,574 - 2,117,148; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme,

Life assurance

Country-specific benefits

Job summary

ICON plc is seeking a Project Manager, Laboratory to design and analyze clinical trials, interpret complex medical data, and advance innovative therapies. This home-based role in Mexico focuses on coordinating project and programme management delivery, resolving issues, and developing team capability.

You will serve as the primary Sponsor contact, attend sponsor meetings, and manage 10-15 studies in compliance with Good Clinical Practice, communicating progress with sponsors and providing

Qualifications

• Bachelor's degree in a life sciences or healthcare field is required.
• Experience in project management within laboratory or clinical research settings is required.
• Strong communication and interpersonal skills are essential for sponsor meetings and team collaboration.
• Ability to manage multiple studies concurrently while adhering to regulatory standards.

Responsibilities

• Coordinate project and programme management delivery, resolve issues, and develop team capability.
• Act as the Sponsor's main contact for ICON services and day-to-day study management.
• Attend and represent ICON at Sponsor meetings and provide regular management reports to Sponsors.
• Manage 10-15 studies in accordance with Good Clinical Practice.
• Provide ICOLAB support to sponsor personnel.

Skills

Project management

Communication skills

Interpersonal skills

Team leadership

Education

Bachelor's degree in life sciences or healthcare

Job description

ICON plc is seeking a Project Manager, Laboratory to design and analyze clinical trials, interpret complex medical data, and advance innovative therapies. This home-based role in Mexico focuses on coordinating project and programme management delivery, resolving issues, and developing team capability.

You will serve as the primary Sponsor contact, attend sponsor meetings, and manage 10-15 studies in compliance with Good Clinical Practice, communicating progress with sponsors and providing