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Clinical Trial Unit Manager Jobs (NOW HIRING)

Elixir Associates

Clinical Trial Manager

Alameda, CA · On-site

Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program Manager I am running a team build for a clinical-stage medical device company in the Bay Area! Early ...

OCUGEN OPCO INC

Clinical Trial Manager

Malvern, PA

Position Summary The Clinical Trial Manager (CTM) is responsible for the overall operational management and execution of clinical trials from initiation through close-out. This includes leading the ...

Elixir Associates

Clinical Trial Manager

San Jose, CA · On-site

Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program Manager I am running a team build for a clinical-stage medical device company in the Bay Area! Early ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed

Elixir Associates

Clinical Trial Manager

Hayward, CA · On-site

Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program Manager I am running a team build for a clinical-stage medical device company in the Bay Area! Early ...

Elixir Associates

Clinical Trial Manager

Santa Rosa, CA · On-site

Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program Manager I am running a team build for a clinical-stage medical device company in the Bay Area! Early ...

ICON

Clinical Trial Manager

Center Square, PA · On-site

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

Elixir Associates

Clinical Trial Manager

San Mateo, CA · On-site

Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program Manager I am running a team build for a clinical-stage medical device company in the Bay Area! Early ...

Ocugen Inc

Clinical Trial Manager

Malvern, PA · On-site

Position Summary The Clinical Trial Manager (CTM) is responsible for the overall operational management and execution of clinical trials from initiation through close-out. This includes leading the ...

Elixir Associates

Clinical Trial Manager

Sunnyvale, CA · On-site

Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program Manager I am running a team build for a clinical-stage medical device company in the Bay Area! Early ...

Elixir Associates

Clinical Trial Manager

Fremont, CA · On-site

Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program Manager I am running a team build for a clinical-stage medical device company in the Bay Area! Early ...

Ocugen Opco Inc

Clinical Trial Manager

Malvern, AR · On-site

Position SummaryThe Clinical Trial Manager (CTM) is responsible for the overall operational management and execution of clinical trials from initiation through close-out. This includes leading the ...

Arcus Biosciences

Clinical Trial Manager

Hayward, CA · On-site +1

Summary The Clinical Trial Manager (CTM) will provide clinical study support to the Clinical Program Manager/Study Management Team Lead (SMTL) for one or more clinical studies, ensuring efficient ...

Arcus Biosciences

Clinical Trial Manager

Brisbane, CA · On-site +1

Summary The Clinical Trial Manager (CTM) will provide clinical study support to the Clinical Program Manager/Study Management Team Lead (SMTL) for one or more clinical studies, ensuring efficient ...

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How much do clinical trial unit manager jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for clinical trial unit 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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Infographic showing various Clinical Trial Unit Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Manager/Senior Clinical Trial Manager

San Diego, CA • On-site

Janux Therapeutics
Biotechnology Research and Development • 11 - 50 employees
Learn more about Janux Therapeuticsexternal

$140K - $178K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 4 days ago

Job description

The Senior/Clinical Trial Manager will be responsible for managing and executing operational aspects of assigned clinical trials, from study start-up to close-out, with a focus on autoimmune studies. This individual will be instrumental in managing and overseeing CROs, study vendors, and clinical trial sites, while partnering with key internal stakeholders to ensure clinical trial deliverables are completed on time, within budget, and in accordance with regulatory requirements, GCP guidelines, and internal SOPs. This position reports directly to the Senior Director of Clinical Operations and serves as an integral member of the Clinical Operations team, contributing to the development of trial strategy, executing initiatives, and ensuring the highest standards in operational delivery. This is a great opportunity to make a meaningful impact in a fast-paced, mission-driven biotech environment.
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
  • Support the successful execution of clinical trials from protocol concept to clinical study report in support of complex autoimmune programs.
  • Prepare and maintain study-related files and documentation to ensure inspection readiness.
  • Organize and lead study and departmental meetings, including minute-taking and document archiving.
  • Coordinate clinical trial equipment, supplies, and cross-functional project activities (e.g., Clinical Data Review Meetings).
  • Ensure team compliance with study-specific training and perform TMF reviews for completeness.
  • Support clinical sites in preparation for audits and inspections.
  • Assist with budget management and day-to-day clinical operations in compliance with SOPs, ICH/GCP, and regulatory requirements.
  • Track subject and site activity/metrics and perform quality checks across study components.
  • Proactively identify and escalate issues related to functional deliverables.
  • Contribute to study set-up activities including protocol/synopsis development, informed consent forms, system configuration (CTMS, IRT), regulatory submissions, and operational documentation.
  • Collaborate with CROs to ensure timely collection and archiving of TMF documents.
  • Coordinate with regulatory affairs on essential document submissions.
  • Support study close-out activities including TMF and drug reconciliation and CSR readiness.
  • Communicate effectively with study team members and work closely with Clinical Trial Managers and/or Asset Leads.
  • Participate in process improvement and quality initiatives related to study execution.
  • Other duties as deemed necessary.

REQUIRED EDUCATION, EXPERIENCE, SKILLS, AND ABILITIES
  • Bachelor's degree with at least 5 years (CTM) or 8 years (Sr. CTM) of hands-on clinical trial experience, preferably within a pharmaceutical or biotech environment. A combination of CRO and sponsor-side experience will be considered.
  • Demonstrated experience in complex autoimmune clinical trials, including trial set-up, monitoring, and close-out.
  • Strong working knowledge of ICH/GCP regulations.
  • Proficiency with electronic systems such as eTMF, CTMS, EDC, etc.
  • Ability to work independently with minimal oversight and thrive in a collaborative team environment.
  • Strong critical thinking skills, a sense of urgency, and a proactive problem-solving mindset.
  • Excellent interpersonal, written, and verbal communication skills.
  • Proficiency in MS Office and comfort with technology.
  • Minimal travel required (0 to 5%).

$140,000 - $178,000 a year
In addition to a competitive base salary ranging from $140,000 to $154,000 for Clinical Trial Manager and $160,000 to $178,000, we offer stock options, restricted stock units, a stock purchase plan (ESPP) and a target bonus. Janux also provides a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, and supplemental disability insurance. Relocation assistance may also be available.
Please note that the hourly rate range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, and internal equity.
Job Type:Full-time
Benefits:
  • Annual bonus program
  • Incentive stock option plan
  • 401k plan with flat non-elective employer contribution
  • Comprehensive medical insurance with 90-100% employer-paid premiums
  • Dental and vision insurance
  • HSA, FSA, and supplemental insurance plans (life, disability, accident, critical illness, hospital indemnity)
  • Unlimited PTO
  • Generous holiday schedule; includes summer and winter company shutdown
  • Relocation assistance

Schedule:
  • Monday to Friday

Work authorization:
  • United States (Required)

Additional Compensation:
  • Annual targeted bonus %

Work Location:
  • Hybrid preferred in San Diego office. Remote permitted upon approval, with ability to travel 25% for meetings or site visits as required.

EQUAL OPPORTUNITY EMPLOYER:
Janux Therapeutics, Inc. is an equal opportunity employer that is committed to providing a work environment free of harassment and discrimination based upon a protected category, as well as an environment free from retaliation for protected activity.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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