Remote Early-Phase Clinical Project Manager

Parexel; Colorado; Remote; USD 110,000 - 135,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending & Health Savings

Work/Life Balance

401(k) with Company match

Pet Insurance

Job summary

Parexel is seeking a Project Manager, Early Phase to join our team in a remote capacity, based in CA, TX, or CO. You will lead Parexel and sponsor teams in developing tailored operational and logistical strategies for early phase trials, ensuring delivery on time and within budget.

You will be accountable for maintaining compliance with ICH-GCP and regulations, and you will own sponsor relationships while guiding cross-functional teams through the full study life cycle.

Qualifications

• Bachelor's degree in a science-related field is required.
• 2 years of Project Management experience with Parexel or 3–5 years in related fields.
• Early phase experience; site-level experience is highly preferred.
• Experience coordinating clinical trials; knowledge of ICH-GCP preferred.
• Proficiency in Microsoft Office products.

Responsibilities

• Own sponsor relationships, serve as main contact and communicate progress, risks, and solutions.
• Lead sponsor and project team meetings to align objectives, responsibilities and timelines.
• Lead study start-up activities including site selection, contract and budget review, and regulatory approvals.
• Manage project financials, budgets, revenue recognition, milestones and invoicing.
• Monitor timelines, recruitment, data cleaning, CTMS tracking, and provide performance feedback.

Skills

Project management

Clinical research

Cross-functional leadership

Budgeting

Communication

Education

Bachelor's degree in science-related field

Tools

Microsoft Office

CTMS

Job description

Parexel is seeking a Project Manager, Early Phase to join our team in a remote capacity, based in CA, TX, or CO. You will lead Parexel and sponsor teams in developing tailored operational and logistical strategies for early phase trials, ensuring delivery on time and within budget.

You will be accountable for maintaining compliance with ICH-GCP and regulations, and you will own sponsor relationships while guiding cross-functional teams through the full study life cycle.