Manager, Clinical Project Delivery

Immunome • $144K — $167K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 4+ years in clinical project management or clinical trial experience in biotech/pharma.
  • Experience supporting clinical trial vendors, including CROs and central labs.
  • Knowledge of study timeline development and enrollment forecasting methodologies.
  • Experience managing Trial Master Files.
  • Familiarity with clinical development, trial design, and global regulatory frameworks (ICH-GCP, FDA, EMA).
  • Experience supporting CROs across the trial lifecycle.
  • Knowledge of project management practices; PMP Certification is a plus.

Responsibilities

  • Support cross-functional clinical study teams throughout the trial lifecycle.
  • Assist in developing, tracking, and reporting study-level timelines for assigned trials.
  • Maintain accurate enrollment graphs and dashboards for informed decision-making.
  • Monitor project delivery metrics and drive corrective actions for at-risk studies.
  • Facilitate planning, execution, and delivery of clinical trials on time and within budget.
  • Identify operational risks and implement strategies for successful trial delivery.
  • Promote a culture of accountability, collaboration, and continuous improvement.

Benefits

  • Opportunity to work on innovative clinical trials in a dynamic environment.
  • Collaborative culture that values accountability and continuous improvement.
  • Hands-on experience with cross-functional teams and vendor management.
  • Support for professional development and potential PMP certification.
  • Engagement in a mission-driven organization focused on impactful healthcare solutions.
Full Job Description
Position Overview

The Manager, Clinical Project Delivery provides hands-on operational support for the execution of one or more of Immunome's clinical trials, supporting cross-functional clinical trial delivery from planning and initiation through completion-to help ensure studies are executed on time, within budget, and in compliance with regulatory requirements and corporate objectives.

This role contributes to study-level timeline management, helps maintain enrollment projections, supports budget management and vendor performance oversight for assigned trials.

The Manager, Clinical Project Delivery may support one or more studies under the guidance of an Associate Director or above.

Responsibilities

Clinical Project Delivery
  • Support cross-functional facilitation of clinical study teams through the trial lifecycle.
  • Assist with study-level timeline development, tracking, and reporting for assigned trials.
  • Help develop and maintain enrollment graphs and dashboards, ensuring accuracy and timely updates to inform decision-making.
  • Help monitor project delivery metrics (timelines, milestones, enrollment, budget adherence, vendor KPIs) and drive corrective action when studies are at risk.
  • Support cross-functional planning, execution, and delivery of assigned clinical trials on time, within budget, and to quality standards.
  • Help identify operational risks and implement mitigation strategies to ensure successful trial delivery.
  • Champion a culture of accountability, collaboration, and continuous improvement.


Vendor Management
  • Support CRO and Central lab vendor relationships and oversight for assigned studies.
  • Assist with vendor identification, selection, contracting, and onboarding activities in support of Finance, Legal, and clinical study teams.
  • Help monitor vendor performance against contractual obligations, operational timelines, and quality and performance metrics.
  • May support governance meetings, oversight activities, issue escalation, and resolution to ensure timely and effective trial execution.


Quality Assurance and Regulatory Compliance
  • Help ensure adherence to ICH-GCP, FDA, EMA, and global regulatory requirements for assigned trials.
  • May work with Quality Assurance and the Clinical Study Team to ensure ongoing inspection-readiness and implement corrective actions as needed.
  • Support data integrity and consistent trial conduct across assigned trials.


Cross-Functional Collaboration
  • Participate in cross-functional alignment of program objectives and study execution plans.
  • Support cross-functional teams to help identify and mitigate study delivery risks.


Budget and Resource Management
  • Work with CPD and Finance to support management and forecasting of study-level budgets, including change orders, ensuring alignment with corporate priorities and program timelines as assigned.
  • Assist with financial oversight for vendor and study-related activities.
  • Help track and report on budget adherence for assigned studies.


Qualifications
  • Bachelor's degree with at least 4+ years of clinical project management and/or clinical trial experience in the biotechnology or pharmaceutical industry, or an equivalent combination of education and experience.
  • Demonstrated experience supporting clinical trial vendors, including CROs and central labs.
  • Working knowledge of study timeline development, enrollment forecasting and tracking methodologies, and trial risk management.
  • Demonstrated experience supporting management of Trial Master Files.
  • Working knowledge of clinical development, trial design, and global regulatory frameworks (ICH-GCP, FDA, and EMA).
  • Experience supporting CROs and other vendors across the trial lifecycle.
  • Working knowledge of project management practices; PMP Certification a plus.


Knowledge and Skills
  • Ability to effectively work cross-functionally and build relationships with stakeholders without direct authority.
  • Effective communication, negotiation, and interpersonal skills.
  • Detail-oriented with an analytical approach to problem-solving.
  • Ability to prioritize and manage multiple tasks and projects in a fast-paced, dynamic environment.
  • Highly professional, adaptable, and accountable.


Washington State Pay Range

$144,114-$167,693 USD

About Immunome

Immunome is a biotechnology company that develops next-generation cancer immunotherapies. The company's proprietary discovery engine identifies novel cancer targets and develops antibody-based therapies to treat cancer. Immunome's lead product candidate, IMM-BCP-01, is a first-in-class cancer immunotherapy that targets a novel cancer antigen. The company is headquartered in Philadelphia, Pennsylvania.
Learn more about Immunome
Size
20 employees
Market Cap
$33.6 million
Industry
NASDAQ

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