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Clinical Trial Startup Project Manager Jobs (NOW HIRING)

Intuitive

Clinical Trial Manager

San Carlos, CA · On-site

... startup, training, equipment logistics, data management, and operational issue resolution. Clinical ... Strong project management skills (planning, prioritization, stakeholder management) with the ...

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... This role is pivotal in ensuring key project deliverables, primarily from CROs and vendors, are met ...

Intuitive

Clinical Trial Manager

San Carlos, CA · On-site

... startup, training, equipment logistics, data management, and operational issue resolution. Clinical ... Strong project management skills (planning, prioritization, stakeholder management) with the ...

Aditum Bio

Senior Clinical Trial Manager

Cambridge, MA · On-site

Strong understanding of clinical trial startup, execution, closeout, and vendor management in ... Strong organizational, project management, analytical, and problem-solving skills with exceptional ...

Medasource

Clinical Trial Budget Analyst

Sacramento, CA · On-site +1

$62/hr

Study startup and activation support. * Budget amendment management. * Financial records and ... Clinical research finance, budgeting, or project management certifications may be beneficial but ...

Kardigan

Clinical Trial Manager

Princeton, NJ · On-site

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... This role is pivotal in ensuring key project deliverables, primarily from CROs and vendors, are met ...

Peptilogics

Senior Clinical Trial Manager

Pittsburgh, PA · On-site +1

Position Overview The Senior Clinical Trial Manager (Sr CTM) oversees the planning, execution, and ... startup, monitoring, site management, and close-out activities * Anticipate project needs and take ...

Aerogen Pharma Limited

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials ... project management skills, as well as a deep understanding of the regulations and ethical ...

Verastem

Clinical Trial Manager

Boston, MA · On-site

$100K - $125K/yr

Works with senior Clinical Operations members to lead the clinical project team members in the ... Global Phase 3 clinical trial management experience * Minimum of 3 years of clinical trial ...

Peptilogics

Senior Clinical Trial Manager

Pittsburgh, PA · On-site

Position Overview The Senior Clinical Trial Manager (Sr CTM) oversees the planning, execution, and ... startup, monitoring, site management, and close-out activities * Anticipate project needs and take ...

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How much do clinical trial startup project manager jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical trial startup project manager in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

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For Clinical Trial Startup Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Clinical Trial Startup Project Manager job openings in the United States as of June 2026, with employment types broken down into 98% Full Time, and 2% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Manager/Senior Clinical Trial Manager

Waltham, MA • On-site

Oruka Therapeutics
See more jobs at Oruka Therapeuticsexternal

Full-time

Re-posted 4 days ago

Job description

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 www.orukatx.com
As we build our core team, we're 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: Clinical Trial Manager/Senior Clinical Trial Manager
Location: Hybrid 3 days/week if located near office in Waltham, MA or Menlo Park, CA will be required. Remote may be considered.
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 www.orukatx.com
As we build our core team, we're 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.
Role Overview:
Will ensure trial compliance, regulatory alignment, and operational efficiency while collaborating with cross-functional teams to advance Oruka's clinical pipeline. Independently manage the clinical trial by effectively planning and executing the study to ensure quality of deliverables within the specified budget and timeframe. May serve as the clinical functional lead and lead clinical trial initiatives for Oruka's cutting-edge dermatology treatments.
Key Responsibilities:
  • Clinical Trial Management:
    • Lead and manage multiple clinical trials from initiation through to completion, ensuring adherence to study timelines and budgets.
    • Collaborate with investigators, vendors, and cross-functional teams to ensure study execution and operational excellence.
    • Oversee the preparation and review of trial-related documentation, including protocols, informed consent forms (ICFs), case report forms (CRFs), and study reports.
    • In partnership with Program Management, develop and drive cross functional study timelines related to trial setup and execution.
  • Team Leadership:
    • Drive the cross functional internal study team ensuring appropriate alignment, risk management and coordination across all participating functions.
    • Successfully interface with Data Management, Biostatistics and Clinical Development to ensure seamless monitoring and data cleaning initiatives to meet study deliverables and timelines
    • Foster a collaborative team environment focused on operational efficiency and continuous improvement.
  • Regulatory and Compliance Oversight:
    • Ensure that clinical trials are conducted in compliance with all applicable regulations, including FDA, EMA, and ICH-GCP guidelines.
    • Support the preparation and submission of clinical trial applications, including INDs, NDAs, and other regulatory documents with functional leads.
    • Manage interactions with Regulatory Affairs and external vendors to ensure timely submissions and approvals.
  • Budget and Resource Management:
    • Develop and manage clinical trial budgets, ensuring efficient use of resources and timely financial reporting.
    • Monitor and control trial costs to ensure alignment with project forecasts and company objectives.
    • Negotiate contracts and budgets with clinical vendors and investigators.
  • Vendor and Site Management:
    • Oversee the selection and management of clinical vendors (CROs, laboratories, etc.) and ensure they meet performance expectations.
    • Develop strong relationships with clinical sites and external partners to ensure aggressive site startup, high-quality data collection and trial conduct.
    • Perform risk assessment and management, addressing issues proactively to mitigate operational issues.

Qualifications:
  • Bachelor's or Master's degree in life sciences or a related field.
  • 5-7+ years of experience in clinical operations, with a focus on managing complex clinical trials.
  • Expertise in GCP and regulatory requirements.
  • Strong leadership and team management skills.

Compensation:
  • An appropriate financial package will be developed for the successful candidate to include a competitive base salary and equity, with a performance-related bonus opportunity.
  • The anticipated salary range for Manager level is $146,000 - $161,000 and Sr. Manager level is $161,000 - $187,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Oruka is a multi-state employer and this salary range may not reflect positions that work in other states.

Job Location:
  • Hybrid 3 days/week if located near office in Waltham, MA or Menlo Park, CA will be required. Remote may be considered.

We're looking forward to hearing how you can contribute to our team and mission. Join us in shaping the future of our company and making a real impact every day.
Salary Range for the Role
$146,000-$187,000 USD
What We Offer:
  • A chance to be part of a vibrant startup culture where your work can directly impact bringing new medicines to patients.
  • Competitive salary and benefits package.
  • A supportive and inclusive team environment where everyone is encouraged to bring their authentic selves to work.
  • Opportunities for professional growth and development.

Apply