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Clinical Trial Process Owner Jobs (NOW HIRING)

Jobtailor

Clinical Trial Specialist

California, MO · On-site

Contribute to process improvement and training. * Lead or participate in special initiatives and ... Clinical Trial Management * Site Monitoring * Regulatory Compliance * Clinical Research Experience

Icon plc

Clinical Trial Liaison

Blue Bell, PA · On-site

Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes. Your Profile: You will bring relevant clinical research experience, along with the ...

Aerogen Pharma Limited

Participate in the RFP and vendor selection process. * Train new clinical trial staff on study specific processes. * Other responsibilities as assigned. What education and experience are required?

C4-Therapeutics-Inc

Clinical Trial Manager

Watertown, MA · On-site

$138K - $153K/yr

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Clinical Trial Manager Full Time ...

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ · On-site

$95K - $115K/yr

Lead study startup processes, including but not limited to conduct of the clinical trial Investigator meeting together with clinical and medical leadership, site selection, and finalization of site ...

Biopharma Careers

Clinical Trial Specialist

Cincinnati, OH · On-site

$32.25 - $44/hr

Contribute to process improvement and training. * Lead and/or participate in special initiatives as ... clinical trial regulations is required. * Previous experience in medical device monitoring is ...

C4 Therapeutics Inc

Clinical Trial Manager

Watertown, MA · On-site

$138K - $153K/yr

Supporting protocol deviation identification, processing, categorization, and documentation ... Preferred: * Experience with oncology clinical trial management and/or global clinical trials.

ICON

Clinical Trial Manager

Blue Bell, PA · On-site +1

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities ... If you require reasonable accommodations during the recruitment process, please let us know or ...

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How much do clinical trial process owner jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for clinical trial process owner 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.

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Infographic showing various Clinical Trial Process Owner job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Trial Associate / Senior Project Specialist - East Coast US - FSP

Remote

Parexel
Pharmaceutical and Medicine Manufacturing • 10K+ employees
Learn more about Parexelexternal

$34.25 - $46.75/hr

Full-time

Posted 11 days ago

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Candidates must be East Coast US based.

Job Summary:

The Clinical Trial Associate (CTA) provides operational and administrative support to clinical trials throughout their lifecycle, ensuring consistency with applicable regulatory guidelines (ICH-GCP, client SOPs) and facilitates smooth execution of trial activities. Study management activities may include maintenance of information databases and trial tracking reports, coordination of clinical trial documentation and general support to ensure the successful and timely execution of clinical activities and deliverables.

Key Responsibilities:

  • Assist with organizing, updating and maintaining tracking systems and tools to support the conduct of clinical study from start-up to closeout
  • Assist with the coordination and development of study management tools, monitoring tools, study manuals and training materials and presentations
  • Schedule meetings, prepare and distribute meeting agendas, minutes, and follow-up action items for study teams
  • Set up, organize and maintain study files and shared spaces in accordance with study requirements
  • Coordinate and track study training
  • Manage study sample and supply tracking and support interactions with vendors as needed
  • Support the Study Management team with specific projects
  • Effectively communicate with study team members and in collaboration with the study team, identifies and addresses study-related issues
  • Perform routine quality checks on trial level documents to ensure completeness and accuracy
  • Supports the timely, complete and compliant archiving in the TMF
  • Participate in company, departmental and project team meetings including Investigator Meetings
  • May assist with basic financial and budget tracking activities related to the clinical trial.

Skills and Experience Required:

  • BS/BA degree or degree in healthcare field required
  • Experience supporting clinical operations activities in a similar role, 1+ years in a pharma or biotech organization or 2 years of experience in a CRO environment
  • Basic knowledge of drug development and clinical operations processes
  • Foundational knowledge of clinical trial process and supports study activities in accordance with ICH-GCP and Code of Federal regulations
  • Effective written and verbal communication skills, with the ability to work collaboratively within study teams
  • Strong organization and interpersonal skills
  • Foundational experience with eTMF systems (VeevaVault preferred) and basic knowledge of essential documents to file study documents accurately with guidance
  • Strong attention to detail
  • Able to prioritize and manage multiple tasks with competing deadlines
  • High sense of urgency and commitment to excellence in the successful execution of deliverables
  • Demonstrates ability to identify issues and escalate appropriately to support timeline adherence
  • Proficient with MS Office Suite (Excel, Word, PowerPoint) and project tracking tools

EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

What Parexel employees say

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About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

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