Mid Level Clinical Trial Manager Jobs
Mid level clinical trial manager jobs go to professionals ready to own trial protocols end to end, coordinate cross-functional teams, and resolve site-level issues with minimal oversight. Openings run across Biotechnology & Pharmaceuticals, Healthcare & Medical Services, and Science & Research, with 31% remote or hybrid availability, and employers like Medpace, Iqvia, and Moderna hiring at this level now.
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You’ve done this before — now do it with more ownership. You’ll run the TMF for your studies end-to-end, work directly with CROs to resolve problems before they become problems, and help the CTAs around you get better at the job.
Position Description
You’ll independently own key operational pieces of our trials — from TMF integrity to vendor coordination — and mentor junior team members along the way.
The Opportunity
- Own the study TMF plan end-to-end: development, tracking, and archiving of Essential Documents across the trial lifecycle
- Lead quality reviews of the TMF and resolve discrepancies directly with the CRO
- Draft and finalize study documents — plans, manuals, CRFs, and patient materials — with minimal oversight
- Serve as a go-to resource for junior CTAs, providing informal mentorship and process guidance
- Independently manage clinical supply and lab sample coordination, flagging risks before they escalate
- Own data reconciliation issues across systems, looping in Data Management only when needed
- Represent Clinical Operations at portions of team meetings and Investigator Meetings
- Help shape training materials and SOPs used across the broader CTA team
What You’ll Bring
- Bachelor’s degree (BS/BA) or equivalent combination of education and work experience in a science-related field
- 3–5+ years of Clinical Operations or clinical research-related experience
- Demonstrated ownership of a TMF or vendor relationship from start to finish
- Comfortable resolving routine CRO/vendor issues independently before escalating
- Experience mentoring or informally guiding junior team members
- Excellent verbal and written communication skills
- Proficiency with MS Word, Excel, Outlook, and PowerPoint
Salary Range: $134,500 - $146,600 annually
The posted range applies to roles based in the San Francisco Bay Area and reflects local market conditions. Where an offer lands within that range depends on the candidate’s relevant experience, technical expertise, and how their background aligns with the role’s requirements.
Location: Onsite - Brisbane, CA
Fit with Nurix Culture and Values
- Strong team orientation; highly collaborative
- Solutions and results-oriented focus
- Hands-on approach; resourceful and open to diverse points of view
About Nurix Therapeutics
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease.
You’ve done this before — now do it with more ownership. You’ll run the TMF for your studies end-to-end, work directly with CROs to resolve problems before they become problems, and help the CTAs around you get better at the job.
Position Description
You’ll independently own key operational pieces of our trials — from TMF integrity to vendor coordination — and mentor junior team members along the way.
The Opportunity
- Own the study TMF plan end-to-end: development, tracking, and archiving of Essential Documents across the trial lifecycle
- Lead quality reviews of the TMF and resolve discrepancies directly with the CRO
- Draft and finalize study documents — plans, manuals, CRFs, and patient materials — with minimal oversight
- Serve as a go-to resource for junior CTAs, providing informal mentorship and process guidance
- Independently manage clinical supply and lab sample coordination, flagging risks before they escalate
- Own data reconciliation issues across systems, looping in Data Management only when needed
- Represent Clinical Operations at portions of team meetings and Investigator Meetings
- Help shape training materials and SOPs used across the broader CTA team
What You’ll Bring
- Bachelor’s degree (BS/BA) or equivalent combination of education and work experience in a science-related field
- 3–5+ years of Clinical Operations or clinical research-related experience
- Demonstrated ownership of a TMF or vendor relationship from start to finish
- Comfortable resolving routine CRO/vendor issues independently before escalating
- Experience mentoring or informally guiding junior team members
- Excellent verbal and written communication skills
- Proficiency with MS Word, Excel, Outlook, and PowerPoint
Salary Range: $134,500 - $146,600 annually
The posted range applies to roles based in the San Francisco Bay Area and reflects local market conditions. Where an offer lands within that range depends on the candidate’s relevant experience, technical expertise, and how their background aligns with the role’s requirements.
Location: Onsite - Brisbane, CA
Fit with Nurix Culture and Values
- Strong team orientation; highly collaborative
- Solutions and results-oriented focus
- Hands-on approach; resourceful and open to diverse points of view
About Nurix Therapeutics
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease.
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- Biotechnology & Pharmaceuticals
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- Science & Research
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Mid Level Clinical Trial Manager Jobs: Frequently Asked Questions
How do I get a mid level clinical trial manager job?
Position your experience around direct trial ownership, not just support tasks. Highlight protocols you managed from startup through closeout, vendor relationships you led, and any regulatory submissions you contributed to. Applications that show concrete responsibility for timelines, budgets, or site performance stand out. Tailor your materials to the therapeutic area and phase focus listed in each job description.
Which companies hire mid level clinical trial managers?
Companies hiring mid level clinical trial managers right now include Medpace, Iqvia, and Moderna, based on current listings on Migrate Mate as of September 2026. Hiring at this level comes primarily from contract research organizations, mid-size biotechs, and large pharmaceutical sponsors running active Phase II and Phase III programs.
Are there remote mid level clinical trial manager jobs?
Yes, though most roles still include periodic site travel. About 31% of mid level clinical trial manager openings are remote or hybrid as of September 2026, reflecting industry adoption of remote monitoring models. Fully on-site roles tend to be concentrated at sponsor sites running early-phase or complex device trials.
How do I move up to a mid level clinical trial manager role?
The path typically runs through demonstrated ownership rather than time alone. Build it by taking lead responsibility on a protocol or site activation, completing a Good Clinical Practice certification, and accumulating measurable results like on-time enrollment or clean audit records. Volunteering for cross-functional projects and mentoring newer coordinators signals readiness for the accountability mid level roles require.
Which industries hire the most mid level clinical trial managers?
Mid Level clinical trial manager roles concentrate in Biotechnology & Pharmaceuticals, Healthcare & Medical Services, and Science & Research, based on current listings on Migrate Mate as of September 2026. Those sectors drive hiring at this level because they run the highest volumes of interventional studies requiring experienced managers who can operate with limited oversight across multiple active sites.