Manager, Project Management

Eclinicalsolutions; United States; Remote; USD 150,000 - 165,000; Full time

Job summary

Eclinicalsolutions is seeking a senior Lead Project Manager to guide a team delivering clinical data and biometrics services across complex trials. You will oversee study start-up through database lock, ensuring reliable execution and strong client communication.

Fluency in managing cross-functional teams, risk management, and adherence to ICH/GCP, 21 CFR Part 11 are essential. This role supports a remote-friendly culture with emphasis on delivering high-quality programs.

Qualifications

• Bachelor’s degree or equivalent experience required.
• PMP certification preferred.
• Extensive project management experience in clinical/biomedical/software settings.

Responsibilities

• Lead project managers and oversee delivery across trial programs.
• Coordinate cross-functional delivery with sponsors, CROs, and vendors.
• Identify and manage risks related to data quality, timelines, and staffing.
• Maintain client relationships and drive continuous improvement in delivery.

Skills

Leadership

Program management

Communication

Stakeholder management

Risk management

Microsoft Office

Education

Bachelor’s degree

PMP certification

Tools

Microsoft Project

Collaboration platforms

Job description

Role overview

Lead project managers delivering clinical data and biometrics services across complex clinical trial programs. This role combines people leadership with oversight of high-profile client work, coordinating delivery from study start-up through database lock and support for regulatory submissions. Success depends on reliable execution, clear client communication, and continuous improvement in a regulated environment.

Responsibilities

• Coach, mentor, and assess project managers, reinforcing consistent project management practices and delivery standards.
• Oversee complex trial projects and ensure plans align with protocols, client expectations, and applicable regulations.
• Coordinate dependencies across electronic data capture, interactive response technology, sponsors, contract research organizations, biostatistics, and data review.
• Identify and manage risks involving data quality, timelines, staffing, and external vendors.
• Guide study start-up planning, clarifying schedules, cross-functional responsibilities, and accountability.
• Maintain transparent client relationships, address issues early, and use lessons from completed studies to improve delivery.

Requirements

• Extensive project management experience; the listing prefers 10 or more years in clinical, biomedical, or software settings.
• The listing prefers at least five years in pharmaceuticals, biotechnology, or equivalent senior consulting work, and three or more years leading people.
• Strong knowledge of clinical trial methods and lifecycle, ICH/GCP guidance, 21 CFR Part 11, and CRO, IRT, and EDC delivery models.
• Demonstrated ability to manage complex clinical data or trial programs using established project management methods.
• Strong communication, negotiation, stakeholder management, and judgment in ambiguous or high-pressure client situations.
• Comfort with Microsoft productivity and project tools, collaboration platforms, and operational systems.

A bachelor’s degree or equivalent experience and PMP certification are preferred.

Benefits and work setup

• The listing gives a U.S. pay range of $150,000–$165,000.
• The employer describes an inclusive, people-focused culture and recognition for remote work.