Clinical Research Associate II

Zohorecruit; Louisville (KY); On-site; USD 52,000 - 76,000; Full time

Job summary

Zohorecruit in Louisville, KY is seeking a Clinical Research Support professional to assist in design, monitoring, and documentation for multiple trials. You will coordinate site initiation, regulatory materials, and study logistics to ensure compliance with US and international guidelines.

Qualified candidates have 1–3 years of clinical research experience, knowledge of GCPs, and strong communication skills.

Qualifications

• BA/BS, RN, BSN or equivalent required.
• 1-2 years of clinical research experience or training.
• Basic knowledge of GCPs.
• Excellent written and verbal communication skills.

Responsibilities

• Assist in design and preparation of protocols and case report forms.
• Generate clinical SOPs, policies, charters, and plans according to US and international guidelines.
• Participate in the evaluation of potential clinical sites according to established criteria of acceptability.
• Procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions.
• Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
• Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions.
• Prepare site visit reports with identification of key accomplishments, key issues for resolution and recommendations for follow-up actions for assigned study sites.
• Conduct study termination visits, obtain final reports from investigators, and participate in the preparation of final reports for regulatory submission.
• Assist with the maintenance of clinical archive and electronic files.
• Other tasks as assigned.

Skills

Attention to detail

Multitasking

Communication skills

Education

BA/BS or RN (BSN) or equivalent

Job description

Louisville, United States | Posted on 03/12/2026

• Industry Pharma/Biotech/Clinical Research
• Work Experience 1-3 years
• State/Province Kentucky
• Country United States

Job Description

Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team.

• Participate and assist in design and preparation of protocols and case report forms.
  
• Generate clinical SOPs, policies, charters, and plans according to US and international guidelines.
  
• Participate in the evaluation of potential clinical sites according to established criteria of acceptability.
  
• Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions.
  
• Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
  
• Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions.
  
• Prepare site visit reports with identification of key accomplishments, key issues for resolution and recommendations for follow-up actions for assigned study sites.
  
• Conduct study termination visits, obtain final reports from investigators, and participate in the preparation of final reports for regulatory submission.
  
• Assist with the maintenance of clinical archive and electronic files.
  
• Other tasks as assigned.
  

Requirements

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• BA, BS, RN, BSN or equivalent
  
• Basic knowledge and adherence to GCPs
  
• 1-2 years of clinical research experience or equivalent experience or training
  
• Strong attention to detail
  
• Ability to multi-task
  
• Unquestionable integrity and highest ethical standards
  
• Excellent written and verbal communication skills