Skip to main content
cGxPjobs.com
Log inSign up

Back

Jobs at Odyssey Therapeutics

Showing 5 JobsSort by:

Senior Director, Clinical Operations

  • Odyssey Therapeutics

    • Remote
    • Massachusetts

Principal Scientist/Associate Director, Process Chemistry

  • Odyssey Therapeutics

    • On-site
    • Boston, MA

Executive Director, Biologics DMPK & Translational Sciences

  • Odyssey Therapeutics

    • On-site
    • Boston, MA

Clinical Trial Manager II

  • Odyssey Therapeutics

    • On-site
    • Boston, MA

Director/Senior Director, IT

  • Odyssey Therapeutics

    • On-site
    • Boston, MA

1–5 of 5 jobs

Senior Director, Clinical Operations

  • Odyssey Therapeutics

Open in New Tab

Remote

$176,554 - 220,692/ Year

Bio-Pharma

Pre-Clinical

  • Posted on:

Job Description

Summary

We are seeking an experienced Senior Director, Global Clinical Development Operations to provide leadership and strategic direction for the operational execution of Odyssey's clinical development programs. Reporting to the VP, Global Clinical Development Operations and working closely with the designated Program Leader and cross-functional leadership, you will ensure alignment and accountability for program execution and operate effectively within a matrix organization.This is a senior role responsible for establishing the clinical operations strategy for studies and ensuring the successful execution of complex clinical trials across the development portfolio.

Responsibilities
  • Provide strategic and operational leadership for Odyssey's clinical development programs, with particular accountability for the successful execution of Phase 3 clinical trials.
  • Own clinical trial patient recruitment and enrollment strategy and performance, proactively identifying barriers to enrollment and mobilizing cross-functional teams, investigators, CROs, and other partners to resolve blockers and keep studies on track.
  • Translate clinical development strategy into clear, executable operational plans, ensuring programs are delivered with the highest standards of quality, patient safety, data integrity, and operational rigor.
  • Partner closely with Clinical Development and cross-functional leaders to shape study strategy, assess operational feasibility, anticipate risks, and identify opportunities to accelerate development.
  • Provide strategic oversight of CROs, vendors, investigators, and other external partners, ensuring accountability for timelines, budgets, quality, and deliverables.
  • Proactively identify and resolve complex operational challenges, providing clear recommendations and communicating program progress, risks, and resource needs to senior and executive leadership.
  • Help build and evolve a high-performing, scalable Clinical Operations organization, including directly managing and developing talent, establishing effective processes and ways of working, and preparing the organization to support Odyssey's growing pipeline.
  • Serve as a senior Clinical Operations leader and trusted partner to cross-functional collaborators.
  • Contribute to broader clinical development and organizational strategy as Odyssey advances its pipeline and grows as a company.
Qualifications

Required:

  • Bachelor's degree in a scientific, medical, nursing, or other relevant discipline; advanced degree preferred.
  • 12+ years of progressive clinical operations experience in the biotechnology or pharmaceutical industry.
  • Significant, hands-on experience leading Phase 3 clinical trials, including demonstrated success taking studies through execution and key late-stage milestones.
  • Demonstrated experience leading complex, global, multi-center clinical development programs.
  • Proven ability to develop and execute clinical operations strategies at the program and/or portfolio level.
  • Extensive experience overseeing CROs, vendors, consultants, investigators, and clinical sites.
  • Strong knowledge and practical application of ICH/GCP guidelines and applicable clinical research regulations.
  • Demonstrated experience managing clinical trial budgets, timelines, resources, risks, and operational performance.
  • Proven ability to operate effectively in a fast-paced, evolving biotech environment with a high degree of autonomy and accountability.
  • Demonstrated leadership experience, including the ability to develop talent, build teams, and influence across a matrix organization.
  • Exceptional strategic thinking, judgment, problem-solving, and decision-making skills.
  • Excellent written, verbal, and executive communication skills.
  • Strong ability to influence and collaborate cross-functionally without relying solely on formal authority.
  • Demonstrated commitment to patient safety, data quality, and operational excellence.



Preferred:

  • Experience leading clinical development programs in autoimmune and/or inflammatory diseases.
  • Experience with small-molecule and/or protein therapeutic development.
  • Experience supporting regulatory submissions and health authority interactions.
  • Experience building Clinical Operations capabilities within a growing biotech organization.
  • Experience establishing clinical operations processes, systems, governance models, and organizational infrastructure.
  • Experience managing multiple programs or trials simultaneously within a growing portfolio.
Education

Degree

Bachelor

Specialization

Scientific/medical/nursing
Experience:

13-16 yrs

  • Skills:
  • Phase 3 clinical trials
  • Global clinical trial management
  • CRO oversight
  • Clinical Trial Budget Management
  • Patient Recruitment Strategy
  • Clinical Operations Strategy
  • talent development
  • Job Type:
  • Full-time
  • Shift Type:
  • 8 hour shift
  • Monday to Friday
  • Day shift

Compensation

  • Benefits:
  • 401K
  • 401K Match
  • Medical, Dental, Vision
  • Additional:
  • Base Salary

Job ID:

CGXP_26_34167

© cGxP Tech, Inc. All rights reserved.