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Post Masters Research Associate Jobs in Missouri

... Masters or PhD/MD/PharmD. * At least 4 plus years of onsite monitoring experience is required ... Senior Clinical Research Associate, Senior CRA, Freelance, Self-employed, Contract, Site Management ...

Emphasis will be placed on monomer synthesis, radical-based polymerization methods, post ... Founded in 1853, WashU is a leading private research university renowned for excellence in research ...

Erica Scheller has a post-doctoral opportunity in neuroskeletal biology. The fellow will conduct research projects, including development of project concepts, experimental design, data analysis ...

Location SAINT LOUIS, MO 63110 Position Summary The Cooper lab at WashU is seeking a post-doctoral research fellow with a strong background in immunology and bioinformatics to work on projects ...

Posdoctoral Fellow

Saint Louis, MO · On-site

$47K - $64K/yr

The SLU MMI department has an opening for a post-doctoral research associate. The appointee will work in a collaborative environment and have the opportunity to contribute to multiple projects.

Post Doctoral Fellow

Saint Louis, MO

$47K - $64K/yr

The research associate (postdoctoral fellow) will work closely with a large research team (including SLU Education Policy faculty and graduate students, researchers in the SLU PRiME education policy ...

Post Doctoral Fellow

Saint Louis, MO · On-site

$47K - $64K/yr

The research associate (postdoctoral fellow) will work closely with a large research team (including SLU Education Policy faculty and graduate students, researchers in the SLU PRiME education policy ...

Post Doctoral Fellow

Saint Louis, MO

$47K - $64K/yr

Louis, MO, is seeking a full-time postdoctoral research associate in the fields of tumor immunology and autoimmunity. We study the dendritic cells required to mount adaptive T cell responses in the ...

Post Doctoral Fellow

Saint Louis, MO · On-site

$47K - $64K/yr

Louis, MO, is seeking a full-time postdoctoral research associate in the fields of tumor immunology and autoimmunity. We study the dendritic cells required to mount adaptive T cell responses in the ...

Our findings highlight the importance of subcellular localization and post-translational ... For more information about the lab and our research, please visit the following websites: Working ...

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Post Masters Research Associate information

See Missouri salary details

$15

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$43

How much do post masters research associate jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for post masters research associate in Missouri is $30.52, according to ZipRecruiter salary data. Most workers in this role earn between $24.57 and $34.71 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of a Post Masters Research Associate?

As a Post Masters Research Associate, your daily tasks may include designing and conducting experiments or studies, collecting and analyzing data, and preparing research reports. You’ll often collaborate closely with principal investigators, faculty, or senior researchers, contributing your expertise to ongoing projects. The role also involves presenting findings at meetings, managing project timelines, and occasionally mentoring undergraduate or new graduate team members. This position is an excellent opportunity to gain hands-on research experience and advance your technical and analytical skills in preparation for further academic or professional advancement.

What is a Post Masters Research Associate job?

A Post Masters Research Associate is a research-focused position for individuals who have recently earned a master's degree. They typically work under the guidance of senior researchers or principal investigators, contributing to projects in academia, government labs, or industry. Responsibilities may include data collection, analysis, experimentation, and publishing research findings. This role helps build expertise and experience for those considering further education or a career in research and development.

What are the key skills and qualifications needed to thrive in the Post Masters Research Associate position, and why are they important?

To thrive as a Post Masters Research Associate, you need a relevant master's degree, strong research methodology knowledge, and proficiency in data analysis. Familiarity with statistical software (such as SPSS, R, or Python), laboratory equipment, or specialized technology is often expected depending on the discipline. Excellent written and verbal communication, critical thinking, and the ability to collaborate effectively are crucial soft skills for this role. These abilities enable you to contribute meaningfully to research projects, produce high-quality results, and work smoothly within academic or professional teams.

What are popular job titles related to Post Masters Research Associate jobs in Missouri? For Post Masters Research Associate jobs in Missouri, the most frequently searched job titles are:
Infographic showing various Post Masters Research Associate job openings in Missouri as of July 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 95% In-person, and 5% Hybrid job distribution, with an average salary of $63,489 per year, or $30.5 per hour.

Clinical Research Associate II and Senior Clinical Research Associate

ClinChoice

Other

Re-posted 24 days ago


Job description

Are you a CRA looking for the best of both worlds?

Would you like to work directly with a single sponsor while still enjoying the stability, global reach, and career development opportunities that come with working for a leading CRO? Our team calls it the best of both worlds - and we think you'll agree.

ClinChoice is a rapidly growing global contract research organization. We're currently expanding our CRA network in the Netherlands and looking for talented Clinical Research Associates (CRA II and Senior CRA) interested in partnering with some of the world's leading pharmaceutical companies in the field of biomedicine.

If that sounds like you, we encourage you to submit your resume via our website - we'd love to hear from you!

Position Overview - Clinical Research Associate
As a CRA, you'll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices. You will oversee site performance, conduct company-initiated clinical studies, and ensure high-quality deliverables through site visits, monitoring, and effective communication.

Key Requirements:

  • Willingness to travel to sites and surrounding countries (50-80% travel).

  • Fluent in Dutch (required for work in the Netherlands).

  • Prior experience in monitoring clinical trials and site management.

Join a dynamic, global team that values growth, collaboration, and making a difference in clinical research.

Skills and Qualifications:

  • Bachelor's Degree or equivalent University Degree in scientific and/or medical or paramedical disciplines; Nursing degree or relevant degree or background preferred. In some cases, an equivalency, consisting of a combination of appropriate education, training and or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
  • Up to 8 years of experience as a CRA.
  • Strong knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirements.
  • Sound knowledge of medical terminology.
  • Fluent in English and local language(s).
  • Proficiency in Microsoft Office (e.g. Word, Excel, Outlook).

Education and Experience:

  • A Bachelor Degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science, a Masters or PhD/MD/PharmD.
  • At least 4 plus years of onsite monitoring experience is required.
  • Previous medical device monitoring experience is required. Therapeutic area experience in neuro- or cardiovascular domain is also required.
  • Requires understanding and application of regulations and standards applied in clinical research areas and medical devices/combination products.
  • Relevant industry certifications preferred (i.e., CCRA, RAC, CDE).
  • Clinical/medical background - a plus.
  • Languages: Be able to converse and monitor in English and Dutch. Must be able to converse and understand the documentation, monitoring, etc. in a reasonably confident manner to monitor in that.
  • Ability to travel up to 80% of time.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

Who will you be working for?

About ClinChoice    

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.           

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology.  The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

Keywords: Senior Clinical Research Associate, Senior CRA, Freelance, Self-employed, Contract, Site Management, Monitor, Monitoring, Complex Trials, Medical Devices, Cardiology, Neurology, Open to Travel, Submissions, Ethics, Contract Research Organisation, CRO

 #LI-CM1 #LI-CONTRACT #LI-1FTE