Pharmaceutical Project Manager - Clinical Trials

Placements24; Riverton (UT); Remote; USD 120,000 - 180,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Retirement plan

Bonuses

Job summary

Placements24 is seeking an accomplished Pharmaceutical Project Manager specializing in clinical trials for a remote-first role. Responsibilities include planning, executing, and closing trials across Phases I–IV, with cross-functional leadership and external vendor management.

You will ensure adherence to GCP and regulatory standards while delivering trials on time and within budget. The candidate should have a scientific degree, 7+ years of trial management experience, PMP certification is

Qualifications

• Bachelor’s degree in a scientific field (e.g., Pharmacy, Biology, Chemistry) or related field.
• PMP certification is highly desirable for seniority and regulatory oversight.
• Minimum 7 years of pharmaceutical project management experience with clinical trials.

Responsibilities

• Lead planning, execution, and close-out of multiple clinical trials from Phase I through IV.
• Develop detailed project plans with timelines, budgets, and risk management.
• Manage cross-functional teams and external vendors (CROs, central labs).
• Ensure GCP, ICH, and regulatory compliance; monitor CAPAs.
• Prepare status reports for senior management and stakeholders.
• Manage budgets and track expenditures to meet financial objectives.

Skills

PMP certification

Leadership

Communication

Negotiation

Remote work

Project management

MS Project

JIRA

EDC systems

Education

Bachelor's degree in a scientific discipline

PMP certification

Tools

MS Project

JIRA

EDC systems

Job description

About the Role

Our client, a pioneering biopharmaceutical company focused on developing breakthrough therapies, is seeking an accomplished Pharmaceutical Project Manager specializing in clinical trials to join their esteemed team. This role is primarily remote, offering the flexibility to work from anywhere while driving critical clinical trial projects forward. The successful candidate will be responsible for the planning, execution, and successful completion of complex clinical trials, ensuring they are delivered on time, within budget, and in compliance with all regulatory requirements. You will manage cross-functional teams, coordinate with external vendors, and serve as a key liaison between R&D, clinical operations, and regulatory affairs. This is an exceptional opportunity to play a vital role in bringing innovative medicines to patients globally, all within a remote-first operational framework.

Key Responsibilities

• Lead the planning, execution, and close-out of multiple clinical trials from Phase I through IV.
• Develop detailed project plans, including timelines, budgets, resource allocation, and risk management strategies.
• Manage cross-functional project teams, including clinical operations, data management, biostatistics, regulatory affairs, and medical affairs.
• Oversee the selection and management of external vendors, such as Contract Research Organizations (CROs) and central laboratories.
• Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements.
• Monitor project progress, identify deviations, and implement corrective and preventive actions (CAPAs).
• Prepare and present project status reports to senior management and stakeholders.
• Manage project budgets and track expenditures to ensure financial objectives are met.
• Facilitate effective communication among all project team members and stakeholders.
• Contribute to the continuous improvement of project management processes and best practices within the organization.

Requirements

• Bachelor's degree in a scientific discipline (e.g., Pharmacy, Biology, Chemistry) or related field.
• PMP certification is highly desirable.
• A minimum of 7 years of experience in pharmaceutical project management, with a strong focus on clinical trial management.
• Proven track record of successfully managing multiple complex clinical trials through all phases.
• In-depth knowledge of GCP, ICH guidelines, and regulatory submission processes.
• Experience with CRO and vendor management.
• Excellent leadership, communication, organizational, and negotiation skills.
• Proficiency in project management software (e.g., MS Project, JIRA) and electronic data capture (EDC) systems.
• Ability to manage projects effectively in a fully remote setting.
• Strong analytical and problem-solving abilities.
• Demonstrated ability to work collaboratively in a dynamic team environment.

Benefits

Our client offers a highly competitive salary, excellent health, dental, and vision insurance, a generous retirement savings plan, and performance-based bonuses. We provide extensive opportunities for professional development, including leadership training and exposure to cutting-edge clinical research. Employees benefit from a flexible, remote-first work environment, a culture that values innovation and collaboration, and the profound satisfaction of contributing to life-saving medical advancements. This role allows you to impact global health from your chosen location.