Project Coordinator I, Phase I

Fortrea is a global contract research organization providing clinical development, patient access, and technology solutions across multiple therapeutic areas. The Project Coordinator I will support Phase I clinical trials by coordinating study activities, maintaining documentation, tracking timelines, managing clinical systems, and collaborating with internal teams, external sites, and vendors.

Tags

Health Care

Life Science

Pharmaceutical

Artificial Intelligence (AI)

Accounting

Human Resources

Healthcare

Publishing

Biopharma

Bookkeeping and Payroll

Employment

Freelance

Responsibilities

Coordinate and support delivery of Phase I clinical trials, including external site studies

Develop and maintain key study documents (project plans, communication plans, risk registers)

Track timelines, milestones, and study progress to ensure successful execution

Lead and support study meetings, including agendas, minutes, and follow-up actions

Manage systems such as CTMS and eTMF, ensuring accuracy and compliance

Act as a key point of contact for internal teams and external sites

Support feasibility, start-up activities, and vendor coordination

Contribute to continuous improvement initiatives and help mentor junior team members

Benefits

Remote work based in the United States

Work on cutting-edge early phase studies at the forefront of drug development

Collaborate with experienced teams in a high-impact, fast-paced environment

Gain exposure to the full lifecycle of clinical trials

Grow your career within a global clinical research organization

AI-powered talent hiring platform for life sciences, pharma, and IT.

London, England, GBR

https://lifelancer.com

Total Funding

$0.68M

2025-03-01

Pre Seed· $0.24M

2024-03-01

Pre Seed· $0.11M

2023-03-01

Pre Seed· $0.12M

Leadership Team

Jayesh Pandya

Co-Founder & CEO

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Qualifications

All candidates must reside in the United States

Degree in life sciences or related field (or equivalent experience)

2–3 years of clinical research experience, ideally in early phase studies

Experience supporting project management or study coordination

Knowledge of GCP/ICH guidelines and clinical trial processes

Strong organizational, communication, and problem-solving skills

This role does not provide sponsorship

2–3 years of clinical research experience, ideally in early phase studies.

Required skills

Clinical Research, Early-Phase Clinical Studies, Study Coordination, Clinical Practice (GCP), ICH Guidelines, Clinical Trial Processes

Preferred skills

Project Management

Experience

2-3 years