Clinical Project Manager

Job Title: Clinical Project Manager - Oncology

Location:

• US (East Coast) or UK
• Remote role, with travel as needed

Overview:
Join a dynamic, small biotechnology company focused on innovative early-phase oncology treatments. As a Clinical Project Manager, you will lead the planning, execution, and management of clinical trials, leveraging your oncology expertise to drive successful study outcomes. This company offers a collaborative culture where you will work closely with internal and external teams, ensuring adherence to GCP, regulatory guidelines, and company policies across early-phase oncology trials.

Strategic Responsibilities:

• Develop and implement comprehensive clinical trial plans, including timelines, budgets, and resource allocation
• Establish effective patient recruitment strategies to meet enrollment targets
• Build strong partnerships with clinical sites, investigators, and cross-functional teams
• Represent the company at relevant oncology industry events and conferences

Operational Responsibilities:

• Oversee end-to-end execution of early-phase oncology trials, ensuring adherence to protocols
• Collaborate with internal teams (medical, regulatory, data management) and external partners
• Ensure timely and accurate collection, entry, and reporting of clinical data in compliance with GCP
• Manage clinical trial documentation, site monitoring activities, and regulatory submissions
• Identify potential risks and deviations, implementing corrective and preventive actions as needed

Leadership:

• Mentor and guide junior team members, fostering a collaborative and innovative work environment
• Promote continuous learning and development in oncology clinical trial practices
• Attract and retain top talent with a passion for oncology and clinical operations

Qualifications:

• 4+ years of experience as a Clinical Project Manager in oncology trials, with a focus on early-phase studies
• Strong background in working within small/medium biotechnology environments
• Independent, self-driven worker with excellent communication and project management skills
• In-depth knowledge of GCP and regulatory requirements for clinical trials
• Proven ability to manage clinical operations from startup to study closeout, including patient recruitment and site management

This is a fantastic opportunity to contribute to groundbreaking oncology research at a small biotech company. If you are passionate about oncology and clinical operations, and thrive in a close-knit, collaborative environment, we'd love to hear from you.

Contact:
Nicole Crowley

ncrowley@i-pharmconsulting.com