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Quality Assurance Auditor - Clinical Research Cliantha Research Saint Petersburg, FL Job Details Full-time $26 - $30 an hour 20 hours ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance Flexible schedule Life insurance Qualifications Teamwork Interpersonal skills Customer service Pharmaceutical regulatory compliance ICH guidelines Attention to detail Conflict management Desktop applications Organizational skills Data-driven problem-solving Research data analysis Computer skills Research regulatory compliance FDA regulations Quality assurance experience within healthcare Full Job Description Cliantha Research is seeking a dedicated and detail-oriented Quality Assurance Auditor to join our team. This is an in-person position and you must come to work in office. This is NOT a remote position! This role is crucial in ensuring that all clinical trials and research activities comply with regulatory standards and Good Clinical Practice (GCP) . The ideal candidate will possess a strong background in clinical research, excellent analytical skills, and a thorough understanding of FDA regulations. This position involves overseeing documentation, patient monitoring, and ensuring compliance throughout the clinical development process. Must understand all GCP princiaples! Duties Job Description / Roles and Responsibilities for

Job Title:

1) Prepare and conduct routine internal audits of projects conducted at the site as scheduled. These audits are intended to assess Cliantha Research site's compliance with Good Regulated Practices, Quality System Documents (such as SOPs), study protocols, pertinent industry regulations and guidelines; they include, but are not limited to, the following: i. Pre-study (documentation) audits ii. In-process (procedures and documentation) audits iii. Post-study (documentation) audits iv. Statistics and/or pharmacokinetics v. Clinical study reports vi. Data management audits vii. CDISC audits viii. Trial Master File audits ix. Validation reports 2) Review protocols, informed consent forms, source document templates/logs and other project-specific documentation not otherwise reviewed formally in an audit. 3) Prepare and conduct external audits for clinical trial projects to ensure compliance with SOP, Protocol, ICH GCP, quality system and applicable regulatory requirements 4) Prepare and conduct routine process/system audits, as well as audits of validation and/or qualification of computerized systems and facilities. 5) Prepare and conduct qualification audits of 3rd party vendors that provide goods and/or services that support GxP activities at Cliantha Research. 6) Keep QA Management up to date with findings and follow up on corrective actions. 7) Perform adequate and timely follow-up of audits, and issue Quality Assurance statements/certificates for audits conducted. 8) Create Quality Plans, Audit Plans or Audit Checklists for assigned projects. 9) Coordinate with site QA management in the submission and effective maintenance of quality-related data for the development and tracking of quality metrics. 10) Assist in the hosting of sponsor representatives (monitors, auditors, etc.), IRB personnel and regulatory (e.g.

FDA, EMA, HC

) inspectors. 11) Assist the site and QA management in the identification of quality process improvement opportunities and in the development of new processes, documentation and other tools. 12) Work with the Quality Assurance group in the development/revision and implementation of Standard Operating Procedures as required. 13) Assist with the archiving of study documents, as needed 14) Ensure compliance with appropriate Cliantha Research SOP's, GCP (&/or GLP if applicable) and ICH guidelines. 15) Keep personal training file updated on a regular basis. 16) Work in a safe manner that does not endanger yourself or co-workers. 17) Uphold the company mission statement and conduct yourself at all times in a respectful and business-like manner. Be a positive role model for all staff and interact with colleagues in a collaborative way. 18) Execute other duties as may be required. Any Additional responsibility given by Head of the Department /

Management Qualifications:

• Minimum of Bachelor of Arts or Science Degree in a related field or sufficient equivalent relevant training and experience as judged by the site QA management.
• A minimum of five years experience in a Quality auditing role or equivalent clinical experience in the clinical research industry.
• Expert knowledge of, and remaining current with, regulatory requirements pertaining to clinical and/or pre-clinical research (HPFB, FDA, EMA, MHRA, as well as GCP, GxP, etc.).
• Extensive experience in quality review (QC/audit) of documents, processes and systems in various phases of clinical/pre-clinical trials that will enable only minimal training on the clinical audit program at Cliantha Research.
• Attention to detail and the ability to spot inconsistencies a must.
• Executes job responsibilities with very minimal supervision; instead, provides some degree of supervision/mentorship to other staff.
• Ability to understand and follow basic scientific research protocol and procedure.
• Well-developed analytical and problem solving skills, and have the ability to analyze and interpret scientific data.
• Proactively identifies problems and helps others with problem solving.
• Decisive, good decision making skills, able to provide leadership to others in response to situations and to escalate more critical decisions when relevant
• Highly effective interpersonal, customer service and conflict resolution skills.
• Advanced proficiency in the use of personal computers and relevant software applications.
• Excellent organizational skills, detail oriented, efficient and able to multi-task and prioritize effectively
• Strong written and verbal communication skills
• Excellent interpersonal skills

Job Type:

Full-time Pay:

$26.00 - $30.00 per hour

Benefits:

401(k) Dental insurance Flexible schedule Health insurance Life insurance Paid time off Vision insurance

Work Location:

In person