Mid Level Clinical Research Assistant Jobs
Mid level clinical research assistant jobs call for professionals ready to take full ownership of study protocols, coordinate across investigator teams, and keep trials on track with minimal supervision. Openings run across Education, Healthcare & Medical Services, and Biotechnology & Pharmaceuticals, with 30% remote or hybrid availability, and employers like Emory University, University of Miami, and Revival Research Institute hiring at this level now.
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Showing 5 of 162+ Mid Level Clinical Research Assistant jobs
Location:
Toledo Hospital
Department:
Vascular Surgery
Weekly Hours:
40
Status:
Full time
Shift:
Days (United States of America)
Job Summary:
As the Clinical Research Scientist, you implement investigator-initiated clinical research studies through collaboration with physicians, researchers, and research staff.
You will develop hypotheses, research methodology, study design, statistical analysis, writing and publication of results.
The above summary is intended to describe the general nature and level of work performed by the positions. It should not be considered exhaustive.
REQUIREMENTS
- Education: PhD Required
- Skills: Statistical, analysis background with experience in SQL databases, experience in medical writing. Strong inter-personal skills both written and verbal required, effective verbal and written communication skills in English required. Ability to perform statistical analyses, including sample size estimation, for study design and analysis of results.
- Years of Experience: 5 years experience in scientific research methodology and design and data analysis. Proven track record of manuscript preparation and publication. Experience working in medical/healthcare setting.
PREFERRED REQUIREMENTS
- Education: PhD
- Skills: Sponsored clinical trial experience desired and familiarity with clinical setting, medical terminology, and knowledge of vascular disease. Excellent computer skills including Epic EMR, Red Cap, and experience with using large datasets preferred. Healthcare experience related to cardiovascular disease processes.
- Years of Experience: 5+ years
Benefits:
We provide flexible benefits that include compensation and programs to help you take care of your family, your finances and your personal well-being. It’s what makes us one of the best places to work, and helps our employees live and work to their fullest potential.
Qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, religion, sex/gender (including pregnancy), sexual orientation, gender identity or gender expression, age, physical or mental disability, military or protected veteran status, citizenship, familial or marital status, genetics, or any other legally protected category. In compliance with the Americans with Disabilities Act Amendment Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a job with ProMedica, please contact employment@promedica.org
Equal Opportunity Employer/Drug-Free Workplace
Location:
Toledo Hospital
Department:
Vascular Surgery
Weekly Hours:
40
Status:
Full time
Shift:
Days (United States of America)
Job Summary:
As the Clinical Research Scientist, you implement investigator-initiated clinical research studies through collaboration with physicians, researchers, and research staff.
You will develop hypotheses, research methodology, study design, statistical analysis, writing and publication of results.
The above summary is intended to describe the general nature and level of work performed by the positions. It should not be considered exhaustive.
REQUIREMENTS
- Education: PhD Required
- Skills: Statistical, analysis background with experience in SQL databases, experience in medical writing. Strong inter-personal skills both written and verbal required, effective verbal and written communication skills in English required. Ability to perform statistical analyses, including sample size estimation, for study design and analysis of results.
- Years of Experience: 5 years experience in scientific research methodology and design and data analysis. Proven track record of manuscript preparation and publication. Experience working in medical/healthcare setting.
PREFERRED REQUIREMENTS
- Education: PhD
- Skills: Sponsored clinical trial experience desired and familiarity with clinical setting, medical terminology, and knowledge of vascular disease. Excellent computer skills including Epic EMR, Red Cap, and experience with using large datasets preferred. Healthcare experience related to cardiovascular disease processes.
- Years of Experience: 5+ years
Benefits:
We provide flexible benefits that include compensation and programs to help you take care of your family, your finances and your personal well-being. It’s what makes us one of the best places to work, and helps our employees live and work to their fullest potential.
Qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, religion, sex/gender (including pregnancy), sexual orientation, gender identity or gender expression, age, physical or mental disability, military or protected veteran status, citizenship, familial or marital status, genetics, or any other legally protected category. In compliance with the Americans with Disabilities Act Amendment Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a job with ProMedica, please contact employment@promedica.org
Equal Opportunity Employer/Drug-Free Workplace
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Find JobsMid Level Clinical Research Assistant Job Market
Who's Hiring
- Emory University17
- University of Miami5
- Revival Research Institute5
- Retina Consultants of Texas4
- University of Alabama, Birmingham4
Top Industries Hiring
- Education51
- Healthcare & Medical Services46
- Biotechnology & Pharmaceuticals15
- Science & Research12
- Medical Devices6
Mid Level Clinical Research Assistant Jobs: Frequently Asked Questions
How do I get a mid level clinical research assistant job?
Position your application around ownership, not just participation. Highlight studies where you managed regulatory submissions, coordinated site activities, or resolved protocol deviations independently. Employers at this level want to see that you can carry a trial from startup through close-out with limited hand-holding. Tailor your resume to show scope, not just tasks, and use specific outcomes like enrollment rates or audit results to demonstrate impact.
Which companies hire mid level clinical research assistants?
Companies hiring mid level clinical research assistants right now include Emory University, University of Miami, and Revival Research Institute, based on current listings on Migrate Mate as of August 2026. Hiring at this level covers contract research organizations, academic medical centers, and mid-size biotech and pharmaceutical companies that need experienced coordinators capable of running studies with limited oversight.
Are there remote mid level clinical research assistant jobs?
Yes, though availability depends on the type of work involved. About 30% of mid level clinical research assistant openings are remote or hybrid as of August 2026, concentrated in roles focused on data management, regulatory coordination, and sponsor liaison work rather than hands-on patient-facing duties. Site-based trials typically require in-person presence at the clinical site.
How do I move up to a mid level clinical research assistant role?
The path to mid level is built through progressive ownership. Start by volunteering for more complex tasks on the studies you already support, such as managing IRB submissions, training newer coordinators, or taking the lead on subject recruitment. Earning a credential like the ACRP CCRC and documenting measurable contributions, such as how many subjects you enrolled or how quickly a site reached readiness, accelerates that transition.
Which industries hire the most mid level clinical research assistants?
Mid Level clinical research assistant roles concentrate in Education, Healthcare & Medical Services, and Biotechnology & Pharmaceuticals, based on current listings on Migrate Mate as of August 2026. These sectors drive demand because they run the highest volumes of regulated clinical trials, require experienced coordinators to maintain protocol compliance, and depend on mid level staff to bridge the gap between entry-level support and senior project oversight.