Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. Primary Responsibilities * Under direction of the study coordinator or ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. Primary Responsibilities * Under direction of the study coordinator or ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. Primary Responsibilities * Under direction of the study coordinator or ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. Primary Responsibilities * Under direction of the study coordinator or ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. Primary Responsibilities * Under direction of the study coordinator or ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. Primary Responsibilities * Under direction of the study coordinator or ...
Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities * Coordinate patient visits to clinic. Organize ...
New
Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities * Coordinate patient visits to clinic. Organize ...
New
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. Primary Responsibilities * Under direction of the study coordinator or ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. Primary Responsibilities * Under direction of the study coordinator or ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. This is a full-time position supporting second-shift operations. Primary ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. This is a full-time position supporting second-shift operations. Primary ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. This is a full-time position supporting second-shift operations. Primary ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. This is a full-time position supporting second-shift operations. Primary ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. This is a full-time position supporting second-shift operations. Primary ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. This is a full-time position supporting second-shift operations. Primary ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. This is a full-time position supporting second-shift operations. Primary ...
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. This is a full-time position supporting second-shift operations. Primary ...
Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities * Coordinate patient visits to clinic. Organize ...
Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities * Coordinate patient visits to clinic. Organize ...
Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities * Coordinate patient visits to clinic. Organize ...
Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities * Coordinate patient visits to clinic. Organize ...
Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities * Coordinate patient visits to clinic. Organize ...
Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities * Coordinate patient visits to clinic. Organize ...
Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities * Coordinate patient visits to clinic. Organize ...
Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities * Coordinate patient visits to clinic. Organize ...
Under the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including processing ...
Under the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including processing ...
Position SummaryUnder the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including ...
Position SummaryUnder the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including ...
Assistant Clinical Research
Milwaukee, WI · On-site
Position Summary Under the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including ...
Assistant Clinical Research
Milwaukee, WI · On-site
Position Summary Under the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including ...
You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ...
You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ...
You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ...
You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ...
You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ...
You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ...
As a Clinical Research Nurse - Home Visits (PRN) , you'll provide high-quality nursing care ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...
As a Clinical Research Nurse - Home Visits (PRN) , you'll provide high-quality nursing care ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...
Clinical Research Assistant information
See Racine, WI salary details
$7.66 - $10.90
7% of jobs
$10.90 - $14.14
2% of jobs
$16.01 is the 25th percentile. Wages below this are outliers.
$14.14 - $17.38
27% of jobs
The median wage is $19.06 / hr.
$17.38 - $20.61
26% of jobs
$23.20 is the 75th percentile. Wages above this are outliers.
$20.61 - $23.85
16% of jobs
$23.85 - $27.09
9% of jobs
$27.09 - $30.33
7% of jobs
$30.33 - $33.56
4% of jobs
$33.56 - $36.80
1% of jobs
$36.80 - $40.04
0% of jobs
$40.04 - $43.28
0% of jobs
$7
$21
$43
How much do clinical research assistant jobs pay per hour?
As of Jul 19, 2026, the average hourly pay for clinical research assistant in Racine, WI is $21.30, according to ZipRecruiter salary data. Most workers in this role earn between $16.25 and $24.33 per hour, depending on experience, location, and employer.
What are Clinical Research Assistants?
Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.
Is CRC an entry level position?
A Clinical Research Assistant (CRA) is often considered an entry-level position in clinical research, suitable for individuals with a bachelor's degree in a related field. The role typically involves supporting study coordination, data collection, and regulatory documentation, with some positions requiring prior internship or related experience. Advancement may require additional certifications or experience in clinical trial management or specific therapeutic areas.
What are the key skills and qualifications needed to thrive as a Clinical Research Assistant, and why are they important?
To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.
What Does a Clinical Research Assistant Do?
A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.
What are some common challenges Clinical Research Assistants face when coordinating multiple studies simultaneously?
Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.
What qualifications do I need to be a clinical research assistant?
A clinical research assistant typically needs a bachelor's degree in health sciences, biology, or a related field. Relevant skills include attention to detail, organizational abilities, and familiarity with clinical trial protocols and data management tools. Some positions may require certification such as the Certified Clinical Research Professional (CCRP).
What is the difference between Clinical Research Assistant vs Clinical Research Coordinator?
| Aspect | Clinical Research Assistant | Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plus | Requires a bachelor's degree; certifications such as CCRP or CCRC are common |
| Work Environment | Assists in data collection, patient scheduling, and administrative tasks in clinical trial settings | Manages study protocols, patient recruitment, and regulatory compliance in clinical trial sites |
| Employer & Industry | Hospitals, research institutions, pharmaceutical companies | Hospitals, research centers, pharmaceutical companies |
Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.
How much money do clinical research assistants make?
Clinical research assistants typically earn a median annual salary of around $45,000 to $55,000, depending on experience, location, and the complexity of the research environment. Entry-level positions may start lower, while those with specialized skills or certifications can earn higher wages.
What do clinical research assistants do?
Clinical research assistants support the conduct of clinical trials by collecting and managing data, preparing study materials, and ensuring compliance with protocols and regulations. They often work under the supervision of investigators and may use electronic data capture systems, requiring attention to detail and knowledge of Good Clinical Practice (GCP) guidelines.
More about Clinical Research Assistant jobs
- How to Become a Clinical Research Assistant
- What are the benefits of becoming a Certified Clinical Research Assistant?
- Is being a Clinical Research Assistant a good job?
- What is the career progression of a Clinical Research Assistant?
- What Is a Clinical Research Assistant and How to Become One
- Clinical Research Assistant Job Description Sample Template
What are the most commonly searched types of Clinical Research jobs in Racine, WI? The most popular types of Clinical Research jobs in Racine, WI are:
What job categories do people searching Clinical Research Assistant jobs in Racine, WI look for? The top searched job categories for Clinical Research Assistant jobs in Racine, WI are:
What cities near Racine, WI are hiring for Clinical Research Assistant jobs? Cities near Racine, WI with the most Clinical Research Assistant job openings:
Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 9 days ago
Medical College Of Wisconsin rating
7.7
Based on 28 frontline employees who took The Breakroom Quiz
228th of 555 rated colleges and universities
Job description
Summary
Assist study coordinators by providing administrative and data collection support for clinical research studies.
Primary Responsibilities
Knowledge - Skills - Abilities
Qualifications
Appropriate experience may be substituted for education on an equivalent basis.
Minimum Required Education: High School Diploma
Minimum Required Experience: 3 years
Required Certification/Licensure(s): CITI training within 90 days of hire
Physical Requirements
Work requires occasionally lifting moderate weight materials, standing, or walking continuously.
Work Environment
Occasional exposure to dust, noise, temperature changes, or contact with water or other liquids. Work is performed in an environmentally controlled environment.
Sensory Acuity
Ability to detect and translate speech or other communication required. May occasionally require the ability to distinguish colors and perceive relative distances between objects.
Why MCW?
For a brief overview of our benefits see: Benefits Overview
For a full list of positions see: MCW Careers
At MCW all of our endeavors, from our internal operations to our interactions with our partners, are driven by our shared organizational values: Caring - Collaborative - Curiosity - Inclusive - Integrity - Respect. We are committed to fostering an inclusive environment that values diversity in backgrounds, experiences, and perspectives through merit-based processes and in alignment with all applicable laws. We believe that embracing human differences is critical to realize our vision of a healthier world, and we recognize that a healthy and thriving community starts from within. Our values define who we are, what we stand for and how we conduct ourselves at MCW. If you believe in embracing individuality and working together according to these principles to improve health for all, then MCW is the place for you. For more information, please visit our institutional website.
MCW as an Equal Opportunity Employer and Commitment to Non-Discrimination:
The Medical College of Wisconsin (MCW) is an Equal Opportunity Employer. We are committed to fostering an inclusive community of outstanding faculty, staff, and students, as well as ensuring equal educational opportunity, employment, and access to services, programs, and activities, without regard to an individual's race, color, national origin, religion, age, disability, sex, gender identity/expression, sexual orientation, marital status, pregnancy, predisposing genetic characteristic, or military status. Employees, students, applicants or other members of the MCW community (including but not limited to vendors, visitors, and guests) may not be subjected to harassment that is prohibited by law or treated adversely or retaliated against based upon a protected characteristic.
Assist study coordinators by providing administrative and data collection support for clinical research studies.
Primary Responsibilities
- Under direction of the study coordinator or principal investigator, conduct research activities to include visit study participant homes, community centers and other community settings to interview, administer surveys, recruit, and enroll and follow-up with study participants as directed.
- Coordinate patient visits to clinic. Organize study participant charts and files, and distribute to appropriate location.
- Coordinate research related projects such as mailings, participant contact information, patient visits and focus groups
- Collect samples from patients as needed. Process and transport samples as directed.
- Collect required data from study coordinators and research nurses. Code and enter onto clinical research forms and into computerized database.
- Order and maintain log of stipend checks and/or gift certificates to be distributed to study participants. Verify accuracy of bills and stipends.
- Provide general clerical support to nurses and investigators. Compose letters to study participants.
- Provide writing and editorial assistance in the preparation of grants, manuscripts and other study related reports. Assist with the creation of brochures, flyers and educational materials. Conduct literature searches.
- Translate oral and written communication to and from English, if required.
- Other duties as assigned.
Knowledge - Skills - Abilities
- Knowledge of biology, chemistry, mathematics, documentation, and records management.
- Data utilization, complex problem solving, critical thinking, resource management, and writing skills.
Qualifications
Appropriate experience may be substituted for education on an equivalent basis.
Minimum Required Education: High School Diploma
Minimum Required Experience: 3 years
Required Certification/Licensure(s): CITI training within 90 days of hire
Physical Requirements
Work requires occasionally lifting moderate weight materials, standing, or walking continuously.
Work Environment
Occasional exposure to dust, noise, temperature changes, or contact with water or other liquids. Work is performed in an environmentally controlled environment.
Sensory Acuity
Ability to detect and translate speech or other communication required. May occasionally require the ability to distinguish colors and perceive relative distances between objects.
Why MCW?
- Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental. Along with Flexible Spending options
- 403B Retirement Package
- Competitive Vacation and Paid Holidays offered
- Tuition Reimbursement
- Paid Parental Leave
- Employee & Family Assistance Program (EFAP)
- Pet Insurance
- On campus Fitness Facility, offering onsite classes
- Additional discounted rates on items such as: Select cell phone plans, local fitness facilities, Milwaukee recreation and entertainment etc.
For a brief overview of our benefits see: Benefits Overview
For a full list of positions see: MCW Careers
At MCW all of our endeavors, from our internal operations to our interactions with our partners, are driven by our shared organizational values: Caring - Collaborative - Curiosity - Inclusive - Integrity - Respect. We are committed to fostering an inclusive environment that values diversity in backgrounds, experiences, and perspectives through merit-based processes and in alignment with all applicable laws. We believe that embracing human differences is critical to realize our vision of a healthier world, and we recognize that a healthy and thriving community starts from within. Our values define who we are, what we stand for and how we conduct ourselves at MCW. If you believe in embracing individuality and working together according to these principles to improve health for all, then MCW is the place for you. For more information, please visit our institutional website.
MCW as an Equal Opportunity Employer and Commitment to Non-Discrimination:
The Medical College of Wisconsin (MCW) is an Equal Opportunity Employer. We are committed to fostering an inclusive community of outstanding faculty, staff, and students, as well as ensuring equal educational opportunity, employment, and access to services, programs, and activities, without regard to an individual's race, color, national origin, religion, age, disability, sex, gender identity/expression, sexual orientation, marital status, pregnancy, predisposing genetic characteristic, or military status. Employees, students, applicants or other members of the MCW community (including but not limited to vendors, visitors, and guests) may not be subjected to harassment that is prohibited by law or treated adversely or retaliated against based upon a protected characteristic.
What Medical College Of Wisconsin employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Medical College of Wisconsin
Sourced by ZipRecruiter
The Medical College of Wisconsin (MCW) is an industry-leading educational institution located in Milwaukee, WI, US. Being part of the medical and health services sector, MCW's primary mission is to educate and train the next generation of healthcare professionals. MCW offers a wide array of degrees and programs within medical and health sciences, covering everything from medical, graduate, pharmacy and health sciences studies, to continuing professional developments and community engagement initiatives. Founded in 1893, MCW boasts a rich, well-entrenched history in shaping the medical education landscape locally and globally. The institution's core values of knowledge-changing life underline its dedication to incorporating innovative approaches in education and research, commitment to diversity and inclusion, service to the community, integrity, stewardship, and collaboration.
Industry
Health care and social assistance
Company size
5,001 - 10,000 Employees
Headquarters location
Milwaukee, WI, US
Year founded
1893