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Associate Research Coordinator Jobs (NOW HIRING)

City of Hope

Assoc Clinical Research Coord

Duarte, CA · On-site

$25.50 - $33.75/hr

Associate Clinical Research Coordinator Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life ...

Cleveland Clinic

Research Coordinator II

Cleveland, OH · On-site

$72K/yr

Three years of experience as a Research Coordinator I OR Associate's or Bachelor's Degree in Healthcare or a science-related field with one year of experience * Demonstrated proficiency with a ...

Mayo Clinic

Clinical Research Coordinator

Rochester, MN · On-site

$27.99 - $41.98/hr

Associate's in Clinical Research from an accredited academic institution without experience OR ... Graduate or diploma from a study coordinator training program is preferred. * One year of clinical ...

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Associate Research Coordinator information

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$21.5K

$80.6K

$112.5K

How much do associate research coordinator jobs pay per year?

As of Jun 15, 2026, the average yearly pay for associate research coordinator in the United States is $80,570.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,000.00 and $99,500.00 per year, depending on experience, location, and employer.

Do you need a degree to be a CRC?

A Certified Research Coordinator (CRC) typically does not require a specific degree, but many employers prefer candidates with a bachelor's degree in health sciences, nursing, or a related field. Relevant experience, strong organizational skills, and knowledge of clinical research protocols are also important for this role.

How does an Associate Research Coordinator typically collaborate with principal investigators and study participants during a research project?

As an Associate Research Coordinator, you play a central role in facilitating communication between principal investigators, study staff, and participants. You will often schedule and organize participant visits, ensure adherence to study protocols, and relay important updates or issues to the research team. Building strong working relationships and maintaining clear, consistent communication are essential, as you’ll be responsible for coordinating logistics, collecting and managing data, and addressing participant questions or concerns throughout the study.

Is CRA an entry level job?

A Clinical Research Associate (CRA) role is typically considered an entry-level or early-career position in clinical research, often requiring a bachelor's degree in a related field. Some employers may prefer candidates with relevant internships or certifications, but many CRAs start with minimal experience and receive on-the-job training.

What is the difference between Associate Research Coordinator vs Research Assistant?

AspectAssociate Research CoordinatorResearch Assistant
Required CredentialsBachelor's degree, some roles may prefer or require a master'sTypically a bachelor's degree or ongoing education
Work EnvironmentInvolved in coordinating research activities, data management, and liaising with teamsAssists with data collection, literature reviews, and supporting research tasks
Employer & Industry UsageUsed in academic, clinical, and industry research settingsCommon in academic labs, clinical trials, and research institutions

The Associate Research Coordinator generally has more responsibilities in coordinating research projects and managing data, often requiring more experience or education. Research Assistants typically support research activities through data collection and administrative tasks. Both roles are essential in research settings but differ in scope and level of responsibility.

What are the key skills and qualifications needed to thrive as an Associate Research Coordinator, and why are they important?

To thrive as an Associate Research Coordinator, you need a solid background in research methodologies, data collection, and regulatory compliance, often supported by a bachelor's degree in a scientific or health-related field. Familiarity with electronic data capture systems, Institutional Review Board (IRB) processes, and tools like Microsoft Excel or REDCap is common. Outstanding organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating study activities and collaborating with diverse teams. These abilities ensure research projects run smoothly, adhere to protocols, and yield reliable, high-quality data.

What does an Associate Research Coordinator do?

An Associate Research Coordinator supports the planning, implementation, and management of research studies. Their responsibilities often include recruiting and enrolling study participants, collecting and managing data, ensuring compliance with protocols, and coordinating with research teams. They play a key role in maintaining accurate records, scheduling study visits, and assisting with regulatory documentation. The position requires strong organizational, communication, and analytical skills to ensure the smooth running of research projects.

Which is better, CRA or CRC?

A Clinical Research Associate (CRA) and a Clinical Research Coordinator (CRC) are both key roles in clinical trials but have different responsibilities. CRAs typically oversee multiple sites, monitor trial progress, and ensure compliance, often requiring travel and certification such as CCRP. CRCs manage day-to-day trial activities at a single site, handle patient interactions, and coordinate data collection, often working regular hours in a clinical setting.

How much does a CRC make?

A Clinical Research Coordinator (CRC) in Houston typically earns between $50,000 and $70,000 annually, depending on experience, certifications, and the employer. Salaries can vary based on the complexity of studies managed and the size of the organization.
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Associate Research Coordinator jobs near you
Infographic showing various Associate Research Coordinator job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 94% Full Time, 4% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $80,570 per year, or $38.7 per hour.
Clinical Research Coordinator

Clinical Research Coordinator

Cardiovascular Associates of America

Davenport, IA • On-site

$23 - $30.50/hr

Contractor

Posted 19 days ago

Job description

Job Title: Clinical Research Coordinator
Location: On-site position in Davenport, Iowa

About CVAUSA:

Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to advancing medical research and improving patient outcomes. As part of our expansion, we are increasing our clinical trial operations and looking for dynamic, results-driven professionals to join our team.

At CVAUSA, we are focused on innovation and excellence in cardiovascular research, and we believe the best results come from individuals who are passionate about making a difference.

The Research Coordinator will be responsible for leading the growth and development of the research program while also working with clinic staff on existing and new clinical trials. As part of CVAUSA’s national network, the Clinical Research Coordinator will have the opportunity to collaborate with teams across the country, making an impact on cardiovascular care both locally and nationwide.

Position Overview:

As a Clinical Research Coordinator, you will play a key role in managing and overseeing all aspects of clinical trials and site operations. You will have the opportunity to take ownership of your projects, driving them forward with innovation, efficiency, and excellence. This is a fantastic opportunity for an ambitious, goal-oriented individual who thrives in an independent, fast-paced environment.

Key Responsibilities:

Clinical Trial Management:
Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure that protocols are followed meticulously.

Site Operations:
Handle day-to-day site management, ensuring that all activities comply with regulatory requirements and study protocols.

Data Management:
Collect, verify, and manage clinical trial data, ensuring it is accurate and complete.

Communication & Reporting:
Act as the primary point of contact for study sponsors, participants, and other stakeholders. Provide regular updates and progress reports.

Regulatory Compliance:
Ensure all documentation, including regulatory submissions and patient records, are kept up-to-date and in compliance with ethical and legal standards.

Problem Solving & Innovation:
Identify areas for process improvement and implement solutions to drive efficiency and enhance trial operations.

What We’re Looking For:

Goal-Driven & Independent:
You thrive in an autonomous work environment and take full ownership of your responsibilities.

Innovative & Results-Driven:
You are eager to contribute to CVAUSA’s growth and bring effective solutions to the table.

Detail-Oriented & Highly Organized:
You have the ability to manage multiple tasks and deadlines without sacrificing quality.

Strong Communicator:
You can effectively communicate with stakeholders at all levels, including sponsors, site staff, and participants.

Experience & Qualifications:
  • Clinical experience in cardiovascular medicine in a licensed or clinical support role (e.g., RN, technologist, medical assistant)
  • Bachelor’s degree in a relevant field (e.g., life sciences, healthcare, or clinical research)
  • Experience managing clinical trials, leading enrollment across multiple studies, and supporting research program development
  • Strong organizational and time management skills
  • Clinical research certification (e.g., CCRP) is a plus
  • Knowledge of GCP, ICH guidelines, and regulatory requirements
Why CVAUSA?

At CVAUSA, we believe in the power of innovation and are looking for professionals eager to make an impact in cardiovascular research. As a rapidly growing organization, you will be at the forefront of cutting-edge clinical trials, contributing to improved patient outcomes.

You will work on-site in Davenport, Iowa, leading a growing cardiovascular research program while collaborating with teams nationwide. We offer competitive compensation, flexible working hours, and a supportive, dynamic environment where your contributions are valued.

If you are ambitious, innovative, and ready to take your career to the next level, we want to hear from you.

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