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Sr. Associate​/Manager Project Management & Operations

Job in Waltham, Middlesex County, Massachusetts, 02254, USA
Listing for: Oruka Therapeutics
Part Time position
Listed on 2026-08-23
Job specializations:
  • Research/Development
    Regulatory Compliance Specialist, Clinical Research
Salary/Wage Range or Industry Benchmark: 130000 - 161000 USD Yearly USD 130000.00 161000.00 YEAR
Job Description & How to Apply Below

About Us

Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases.

For more information, visit

As we build our core team, we are seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture.

Job Title:

Sr. Associate/Manager
- Project Management & Operations

Location:

Waltham, MA
- Hybrid, onsite 3 days/week is required

Position Overview:

We are seeking a highly motivated Sr. Associate/Manager to join our dynamic, growing team as we work to set a new standard in treating chronic skin diseases. This role will be pivotal in developing and managing systems to support critical early-stage and clinical development efforts.

The ideal candidate will have a technical background and experience in operational execution across cross-functional projects. This individual has the ability to work collaboratively to streamline a variety of activities, including project execution, contract negotiation, and vendor management. They should be highly organized, able to manage multiple priorities, and comfortable working in a fast-paced environment. Some experience in drug development in functions such as clinical pharmacology, translational, clinical development, or a related scientific field is preferred.

Our team values in-person collaboration, and we expect this role to work from our Waltham office three days per week. We're looking for someone who shares our passion for developing innovative medicines and is eager to make a meaningful impact.

Key Responsibilities
  • Support Clinical Pharmacology and Nonclinical program execution by assisting the Program Manager with managing development and operational activities across multiple programs.
  • Leverage project management best practices to track and execute key Clinical Pharmacology and Nonclinical initiatives.
  • Interface with preclinical vendors and service providers, to ensure projects stay on track with planned timelines and budgets.
  • Organize and facilitate internal and external project meetings, including agenda development, meeting documentation, and action item tracking.
  • Build and maintain project timelines, tracking deliverables, and key activities against strategic objectives.
  • Facilitate analysis plans, reports and other documents’ reviews and approvals in support of Clinical Pharmacology and Nonclinical program deliverables.
  • Coordinate with Legal to track and manage contracts related to project activities.
  • Contribute to continuous improvement of project management tools and processes, including templates, trackers, and information management
Qualifications
  • BS in scientific or technical field; advanced degrees (PhD, MBA, MS) preferred
  • 2-4 years of relevant experience, preferably within a nonclinical, clinical pharmacology, translational, or clinical development function in the pharmaceutical or biotech industry
  • Proficiency with standard business and project management tools, such as SharePoint, Smartsheet, MS Project, or similar
  • Ability to work independently while knowing when to elevate risks, issues, or delays
  • Excellent verbal and written communication skills, with the ability to prepare clear meeting summaries, trackers, and cross-functional messages
  • Ability to operate in a fast-paced, timeline-driven environment and to adapt to changing program priorities
  • Collaborative, team-focused, and skilled at working across various disciplines within and outside the company

Compensation:

  • An appropriate financial…
Position Requirements
10+ Years work experience
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