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Clinical Trial Startup Jobs (NOW HIRING)

Novocure

Clinical Trial Lead

Wayne, PA · On-site

$147K - $190K/yr

Clinical Trial Lead Hybrid / Full Time / Chesterbrook, PA At Novocure, we're working to extend the ... Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the ...

Sitelabs

Clinical Trial Coordinator

Miami, FL · On-site

$55K - $70K/yr

Role Overview The Clinical Trial Coordinator is responsible for implementing and supporting ... Experience in a startup, healthcare technology, or rapid-scale environment. * Bilingual Spanish ...

Sitelabs

Clinical Trial Coordinator

Orlando, FL · On-site

$55K - $70K/yr

Role Overview The Clinical Trial Coordinator is responsible for implementing and supporting ... Experience in a startup, healthcare technology, or rapid-scale environment. * Bilingual Spanish ...

SiteLabs

Clinical Trial Coordinator

Miami, FL · On-site

$55K - $70K/yr

Role Overview The Clinical Trial Coordinator is responsible for implementing and supporting ... a startup, healthcare technology, or rapid-scale environment. • Bilingual Spanish/English is a ...

Intuitive

Clinical Trial Manager

Sunnyvale, CA · On-site

The Clinical Trial Manager (CTM) will manage the day-to-day planning and execution of clinical ... startup, training, equipment logistics, data management, and operational issue resolution. Clinical ...

Intuitive

Clinical Trial Manager

Sunnyvale, CA · On-site

The Clinical Trial Manager (CTM) will manage the day-to-day planning and execution of clinical ... startup, training, equipment logistics, data management, and operational issue resolution. Clinical ...

Aditum Bio

Senior Clinical Trial Manager

Cambridge, MA · On-site

Strong understanding of clinical trial startup, execution, closeout, and vendor management in global or multi-center studies. * Working knowledge of ICH-GCP, FDA, EMA, and other applicable clinical ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Drive study startup activities, including feasibility, site selection, and timelines. * Manage activities of Phase 1 and 2 clinical trial investigators with a focus on the US to ensure compliance ...

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Clinical Trial Startup information

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How much do clinical trial startup jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for clinical trial startup in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What are some common challenges faced during the clinical trial startup phase and how can they be managed?

One of the main challenges during the clinical trial startup phase is navigating complex regulatory requirements and ensuring timely ethics committee approvals. Delays can also occur due to contract negotiations with sites and gathering essential documentation. Proactively engaging with stakeholders, maintaining clear communication, and leveraging project management tools help mitigate these issues. Collaboration with cross-functional teams, such as regulatory affairs, legal, and clinical operations, is essential for keeping the process on track and ensuring a smooth study launch.

What are the key skills and qualifications needed to thrive in clinical trial startup, and why are they important?

To excel in Clinical Trial Startup, you need a solid understanding of clinical research processes, regulatory requirements, and project management, often supported by a degree in life sciences or a related field. Familiarity with electronic trial master files (eTMF), clinical trial management systems (CTMS), and GCP certifications is highly valuable. Strong organizational skills, attention to detail, and effective cross-functional communication help ensure smooth site activations and compliance. These competencies are crucial for minimizing delays and ensuring the successful and ethical launch of clinical trials.

What is the difference between Clinical Trial Startup vs Clinical Trial Coordinator?

AspectClinical Trial StartupClinical Trial Coordinator
CredentialsBachelor's degree, industry-specific knowledgeBachelor's degree, often certifications in clinical research
Work EnvironmentPlanning phase, project management, cross-functional teamsMonitoring trials, data collection, site communication
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, hospitals, clinical research organizations

While both roles are essential in clinical research, Clinical Trial Startup focuses on initiating and planning new trials, including site selection and regulatory setup. In contrast, Clinical Trial Coordinators manage ongoing trial activities, ensuring protocol adherence and data accuracy. Understanding these differences helps clarify career paths and job expectations in the clinical research industry.

What is clinical trial startup?

Clinical trial startup refers to the initial phase of setting up a clinical research study before patient enrollment begins. This process includes activities such as protocol development, site selection, regulatory submissions, contract negotiations, ethics committee approvals, and preparing trial materials. The goal is to ensure all the necessary legal, regulatory, and logistical requirements are met, so the study can start smoothly and on time. Efficient trial startup is crucial for minimizing delays and optimizing the overall timeline of a clinical trial.
More about Clinical Trial Startup jobs
What cities are hiring for Clinical Trial Startup jobs? Cities with the most Clinical Trial Startup job openings:
What states have the most Clinical Trial Startup jobs? States with the most job openings for Clinical Trial Startup jobs include:
What job categories do people searching Clinical Trial Startup jobs look for? The top searched job categories for Clinical Trial Startup jobs are:
Clinical Trial Startup jobs near you
Infographic showing various Clinical Trial Startup job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Trial Manager/Senior Clinical Trial Manager

Oruka Therapeutics

Waltham, MA • On-site

Full-time

Re-posted 3 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