Remote Early-Phase Clinical Project Manager

Parexel; Topeka (KS); 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 strategies for early phase clinical trials, ensuring on-time, on-budget delivery and regulatory compliance.

You will own sponsor relationships, guide cross-functional teams through the study lifecycle, manage study budgets, and contribute to operational excellence in early phase clinical research.

Qualifications

• Bachelor's degree in a science-related field required or equivalent.
• 2 years of Project Management experience with Parexel or 3–5 years in related fields.
• Early phase experience; site-level experience preferred.
• Knowledge of ICH-GCP and pharmaceutical industry regulations.
• Proficiency in Microsoft Office products.

Responsibilities

• Own sponsor relationship and communicate progress, risks, and solutions.
• Lead sponsor and project team meetings to align objectives and timelines.
• Participate in pre-award strategy and bid defense activities.
• Lead start-up activities including site selection, budget review, and regulatory approvals.
• Direct internal and sponsor kick-off meetings and ensure scope and delivery expectations.

Skills

Clinical research

Project management

Cross-functional leadership

ICH-GCP knowledge

Microsoft Office

Education

Bachelor's degree in a science-related field

Tools

CTMS

Microsoft Excel

Microsoft Word

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 strategies for early phase clinical trials, ensuring on-time, on-budget delivery and regulatory compliance.

You will own sponsor relationships, guide cross-functional teams through the study lifecycle, manage study budgets, and contribute to operational excellence in early phase clinical research.