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Clinical Research Coordinator Jobs in Ridgefield, CT

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$15

$28

$41

How much do clinical research coordinator jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical research coordinator in Ridgefield, CT is $28.57, according to ZipRecruiter salary data. Most workers in this role earn between $23.22 and $30.87 per hour, depending on experience, location, and employer.

What is a clinical research coordinator?

A Clinical Research Coordinator (CRC) is a professional who manages and oversees clinical trials and research studies involving human participants. They are responsible for ensuring that studies are conducted according to protocol, regulatory requirements, and ethical standards. CRCs handle tasks such as recruiting participants, collecting and managing data, coordinating with research teams, and maintaining documentation. Their work is essential in advancing medical knowledge and ensuring the safety and rights of study participants.

What is a clinical research coordinator?

As a clinical research coordinator, your responsibilities and duties include overseeing research volunteers during medical trials for new drugs and medical devices. You train the volunteers and educate them about the trial and the rules they must follow. You also record data that they report and ensure they are doing the research ethically. Your job is to work with trial subjects, oversee the administration of medication or device usage, and conduct data collection accurately so that the results are as sound as possible. You must also report any unethical practices or concerns regarding trial volunteers to the doctors doing this research.

What are some common challenges faced by clinical research coordinators when managing multiple studies simultaneously?

Clinical Research Coordinators often manage several studies at once, which can present challenges in balancing timelines, documentation, and communication with various stakeholders. Keeping track of regulatory requirements, participant schedules, and data integrity for each study requires strong organizational skills and adaptability. Coordinators frequently collaborate with investigators, sponsors, and clinical staff to ensure protocol adherence and resolve issues quickly, making effective multitasking and prioritization essential to success in this role.

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

To thrive as a Clinical Research Coordinator, you need strong organizational abilities, attention to detail, and knowledge of clinical trial processes, often supported by a degree in life sciences or healthcare. Familiarity with regulatory compliance systems (such as GCP), electronic data capture (EDC) tools, and certifications like ACRP or SOCRA are typically required. Excellent communication, problem-solving, and teamwork skills enable effective coordination among investigators, sponsors, and patients. These competencies are crucial for maintaining data integrity, ensuring regulatory adherence, and supporting the overall success of clinical research studies.

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

AspectClinical Research CoordinatorClinical Research Associate
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are commonOften requires a bachelor's or master's degree; certifications like CCRP or RAC are advantageous
Work EnvironmentWorks primarily at research sites, hospitals, or clinicsWorks mainly at sponsor offices, CROs, or monitoring sites
Employer & IndustryResearch institutions, hospitals, clinicsPharmaceutical companies, CROs, biotech firms
Job FocusManages daily study activities, patient recruitment, data collectionMonitors study progress, ensures compliance, verifies data accuracy

While both roles support clinical trials, Clinical Research Coordinators handle on-site study management and patient interactions, whereas Clinical Research Associates focus on monitoring and compliance from a remote or office setting. Understanding these differences helps in choosing the right career path or job search focus.

What qualifications do you need to be a clinical research coordinator?

A clinical research coordinator typically needs a bachelor's degree in health sciences, biology, or a related field. Relevant experience in clinical settings, strong organizational skills, and knowledge of Good Clinical Practice (GCP) guidelines are also important; some positions may require certification such as the Certified Clinical Research Coordinator (CCRC).
More about Clinical Research Coordinator jobs

What are the most commonly searched types of Clinical Research jobs in Ridgefield, CT?

The most popular types of Clinical Research jobs in Ridgefield, CT are:

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The top searched job categories for Clinical Research Coordinator jobs in Ridgefield, CT are:

What cities near Ridgefield, CT are hiring for Clinical Research Coordinator jobs?

Cities near Ridgefield, CT with the most Clinical Research Coordinator job openings:

Clinical Research Coordinator jobs near you
Infographic showing various Clinical Research Coordinator job openings in Ridgefield, CT as of August 2026, with employment types broken down into 57% Full Time, and 43% Contract. Highlights an 100% In-person job distribution, with an average salary of $59,424 per year, or $28.6 per hour.

Clinical Research Coordinator

Ki Health Partners

New Haven, CT • On-site

$45K - $55K/yr

Full-time

Posted 5 days ago

Job description

About the Role:
Ki Health Partners is looking for a passionate and detail-oriented Clinical Research Coordinator to join their growing team in New Haven, CT. This is an exciting opportunity to play a meaningful role in advancing clinical research and improving patient outcomes. If you thrive in a fast-paced, science-driven environment, we want to hear from you!

Responsibilities:
  • Coordinate and manage day-to-day clinical trial operations in compliance with GCP and regulatory guidelines
  • Screen, enroll, and follow up with study participants throughout the duration of clinical studies
  • Collect, record, and maintain accurate study data using electronic data capture (EDC) systems
  • Serve as a primary point of contact for study sponsors, IRBs, and research staff
  • Prepare and submit regulatory documents, including IRB submissions, amendments, and continuing reviews
  • Monitor patient safety and report adverse events in accordance with protocol requirements
  • Support site initiation visits, monitoring visits, and audits conducted by sponsors or regulatory agencies
Requirements:
  • Bachelor's degree in life sciences, healthcare, or a related field
  • Minimum 3–5 years of experience in clinical research coordination or a similar role
  • Familiarity with FDA regulations, ICH-GCP guidelines, and IRB processes
  • Proficiency with EDC systems and clinical trial management software (CTMS)
  • SOCRA or ACRP certification (CCRP or CCRC) preferred
  • Strong organizational skills with exceptional attention to detail
  • Excellent interpersonal and communication skills for working with patients and multidisciplinary teams
About Us:
Ki Health Partners is a forward-thinking healthcare organization dedicated to driving innovation in clinical research and patient care. Our team is committed to fostering a collaborative, mission-driven culture where every employee's contributions make a real difference. At Ki Health Partners, you'll find a supportive environment that values professional growth, scientific excellence, and meaningful impact.