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Clinical Research Associate Jobs in Irmo, SC (NOW HIRING)

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$9

$33

$56

How much do clinical research associate jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for clinical research associate in Irmo, SC is $33.58, according to ZipRecruiter salary data. Most workers in this role earn between $23.56 and $42.98 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
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What are the most commonly searched types of Clinical Research jobs in Irmo, SC?

The most popular types of Clinical Research jobs in Irmo, SC are:

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What cities near Irmo, SC are hiring for Clinical Research Associate jobs?

Cities near Irmo, SC with the most Clinical Research Associate job openings:

Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Irmo, SC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $69,849 per year, or $33.6 per hour.

Research Coordinator

Columbia, SC • On-site

Midlands Neurology and Pain Associates, P.A.
See more jobs at Midlands Neurology and Pain Associates, P.A.external

Full-time

Re-posted 24 days ago

Job description

Seeking a highly organized, detail-oriented Clinical Research Coordinator to join our team and bridge the gap between innovative medical research and compassionate patient care.
As the Clinical Research Coordinator, you will manage the daily operations of our clinical trials. You will work closely with our Principal Investigators (PIs), clinical staff, and industry sponsors to ensure that all research is conducted with the highest degree of integrity, compliance, and patient safety.
Key Responsibilities:
  • Oversee the lifecycle of clinical trials from site initiation to close-out.
  • Screen, enroll, and consent eligible study participants; maintain high retention rates through excellent communication.
  • Ensure accurate and timely entry of Case Report Forms (CRFs) and maintain meticulous regulatory binders.
  • Adhere strictly to ICH-GCP guidelines, HIPAA regulations, and study-specific protocols.
  • Perform or coordinate study-related procedures (vitals, phlebotomy, ECGs, and sample processing).
  • Serve as the primary point of contact for Clinical Research Associates (CRAs) during monitoring visits and audits.
Qualifications:
  • Minimum of 2–3 years of experience in clinical research coordination.
  • Bachelor’s degree in a life science, healthcare, or related field.
  • CCRC or CCRP (ACRP/SoCRA) certification is highly preferred.
  • Proficiency with Electronic Data Capture (EDC) systems and EMR platforms.
  • Strong phlebotomy and laboratory processing skills.
  • Exceptional organizational skills with the ability to manage multiple protocols simultaneously.
  • Professional demeanor, high ethical standards, and a "patient-first" mentality.