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Clinical Research Iv Jobs (NOW HIRING)

Alcanza Clinical Research

Clinical Research Coordinator

Sugar Land, TX · On-site

$21.75 - $29/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Coordinator Department: Operations Employment Type: Full Time Location: Olympus ... We have established a strong presence across Phase I-IV studies and several therapeutic areas ...

Alcanza Clinical Research

Clinical Research Coordinator

Methuen, MA · On-site

$25.25 - $33.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

We have established a strong presence across Phase I-IV studies and several therapeutic areas ... The Clinical Research Coordinator under the direction of the Site Manager/Director and the ...

Alcanza Clinical Research

$23.50 - $31.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

We have established a strong presence across Phase I-IV studies and several therapeutic areas ... The Clinical Research Coordinator under the direction of the Site Manager/Director and the ...

Headlands Research

Clinical Research Coordinator

Lake Worth, FL

$21.50 - $28.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Mondays through Fridays, 8:30am - 4:30pm Location: Onsite in Lake Worth, FL (no capabilities for remote or hybrid work) Reports to: Clinical Research Manager Benefits: Our benefits package for ...

Headlands Research

Clinical Research Coordinator

Lake Worth, FL

$21.50 - $28.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Mondays through Fridays, 8:30am - 4:30pm Location: Onsite in Lake Worth, FL (no capabilities for remote or hybrid work) Reports to: Clinical Research Manager Benefits: Our benefits package for ...

Alcanza Clinical Research

Clinical Research Nurse

Decatur, GA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Nurse Department: Operations Employment Type: Full Time Location: Accel Research ... We have established a strong presence across Phase I-IV studies and several therapeutic areas ...

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Clinical Research Iv information

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How much do clinical research iv jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for clinical research iv in the United States is $44.13, according to ZipRecruiter salary data. Most workers in this role earn between $36.30 and $52.40 per hour, depending on experience, location, and employer.

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

AspectClinical Research IVClinical Research Coordinator
Required CredentialsBachelor's degree, often with clinical or scientific background; certifications like CCRPHigh school diploma or equivalent; often some college or certification in clinical research
Work EnvironmentPharmaceutical companies, CROs, or research institutions; often in clinical trial sitesResearch sites, hospitals, clinics; direct interaction with patients and study teams
Employer & Industry UsageUsed in clinical trial management, often with more responsibilitiesUsed in patient recruitment, data collection, and study coordination

Clinical Research IV professionals typically have more advanced education and handle higher-level responsibilities in managing clinical trials, while Clinical Research Coordinators focus on day-to-day trial operations and patient interactions. Both roles are essential in the clinical research process but differ in scope and experience requirements.

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

To thrive as a Clinical Research IV, you need advanced knowledge of clinical trial design, regulatory compliance, and data management, typically supported by a relevant degree and significant experience in clinical research. Expertise in clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as SOCRA or ACRP are often required. Strong leadership, analytical thinking, and effective communication distinguish top performers in this role. These skills ensure rigorous study conduct, regulatory adherence, and successful collaboration across multidisciplinary research teams.

What is a Clinical Research IV?

A Clinical Research IV is an advanced-level clinical research professional who manages and oversees complex clinical trials and research projects. They are typically responsible for coordinating all aspects of the study, ensuring compliance with regulatory requirements, mentoring junior staff, and serving as a liaison between investigators, sponsors, and regulatory agencies. Clinical Research IVs often have several years of experience and may contribute to protocol development, data analysis, and publication of research findings. Their role is crucial in ensuring the integrity and success of clinical studies.

What are some typical challenges faced by Clinical Research IV professionals, and how can they be addressed?

Clinical Research IV professionals often encounter challenges such as managing complex, multi-site trials, ensuring regulatory compliance, and coordinating large, interdisciplinary teams. To address these, strong organizational skills, clear communication, and a proactive approach to problem-solving are essential. Leveraging project management tools and maintaining up-to-date knowledge of industry regulations can also help streamline processes and ensure successful study outcomes.
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Clinical Research Iv jobs near you
Infographic showing various Clinical Research Iv job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $91,797 per year, or $44.1 per hour.

Clinical Research Coordinator

Alcanza Clinical Research

Roslindale, MA

$25.50 - $33.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 6 days ago

Job description

Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in  MA, NH, MI, VA, SC, FL, GA and AL. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.  

Key Responsibilities
In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: 
  • Screening of patients for study enrollment;
  • Patient consents;
  • Patient follow-up visits;
  • Documenting in source clinic charts;
  • Entering data in EDC and answers queries;
  • Obtaining vital signs and ECGs;
  • May perform basic lab procedures per protocol, such as:  blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; 
  • Requesting and tracking medical record requests;
  • Updating and maintaining logs, chart filings; 
  • Maintaining & ordering study specific supplies;
  • Scheduling subjects for study visits and conducts appointment reminders;
  • Building/updating source as needed;
  • Conducting monitoring visits and resolves issues as needed in a timely manner;
  • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
o    Filing SAE/Deviation reports to Sponsor and IRB as needed;
o    Documenting and reporting adverse events;
o    Reporting non-compliance to appropriate staff in timely manner;
o    Maintaining positive and effective communication with clients and team            
       members;
o    Always practicing ALCOAC principles with all documentation;
  • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
  • Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;
  • Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed;
  • Assist with training of new research assistants and coordinators;
  • Assist with scheduling and planning for visit capacity for assigned studies;
  • May set up, train and maintain all technology needed for studies;
  • May assist with study recruitment, patient enrollment, and tracking as needed;
  • May handle more complex study assignments and volumes;
  • May participate in community outreach / education events;
  • Maintaining confidentiality of patients, customers and company information,       and;
  • Performing all other duties as requested or assigned.


Skills, Knowledge and Expertise
Minimum Qualifications:  A Medical Assistant diploma, LPN/LVN, EMT credential AND 1+ years of clinical research coordination experience, OR an equivalent combination of education and experience, is required.  Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred.  CCRC or CCRP credential and BLS certification preferred. Bi-lingual (English / Spanish) proficiency is a plus.  

 Required Skills: 
  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
  • Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
  • Strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills. 
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines. 

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. 
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.