Clinical Research Coordinator

We are hiring Clinical Research Coordinator.

Please let me know if you are interested or anyone who might be interested.

Client: Major Medical Device Client

Position: Clinical Research Coordinator

Duration: 5 months on W2

Location: Lufkin, TX 75904

Pay Rate: $26.00-$32.00/ Hr on W2

___________________________________________________________________________________________

Job Description

Position Summary

We are seeking an experienced Clinical Research Coordinator (CRC) to support an ongoing clinical study through data entry, query resolution, and a variety of site coordination activities.

The ideal candidate has prior CRC experience, a collaborative mindset, and the ability to work effectively with diverse stakeholders. Success in this role requires strong interpersonal skills, adaptability, diplomacy, and attention to detail.

Essential Responsibilities

• Conduct clinical studies in compliance with FDA, ICH-GCP, and applicable regulatory guidelines.
• Record patient information and test results accurately according to study protocols.
• Maintain investigational product (IP) accountability logs and related documentation, when required.
• Identify and report suspected protocol or regulatory non-compliance to appropriate site personnel.
• Ensure IRB approval is obtained before study initiation and maintain ongoing IRB compliance throughout the study.
• Build positive relationships with patients to support engagement and retention.
• Attend site initiation visits and protocol training sessions.
• Schedule patients and conduct appointment confirmation and follow-up calls, as needed.
• Complete and maintain sponsor documentation in EDC, case report forms (CRFs), and other clinical systems within required timelines.
• Organize and maintain source documents, patient files, and study records with accurate and up-to-date information.
• Follow established SOPs and clinical operating procedures.
• Assist in maintaining a clean, organized, and compliant clinical environment, including proper waste disposal when applicable.

Required Qualifications

• Bachelor's degree or an equivalent qualification in a clinical, medical, or related healthcare field.
• Minimum 2 years of experience as a Clinical Research Coordinator or in a comparable clinical research role.

Knowledge, Skills & Abilities

• Strong understanding of clinical research processes, including GCP, SOPs, informed consent, and safety monitoring.
• Ability to work independently while managing multiple priorities with strong attention to detail.
• Sound judgment and discretion when handling sensitive and complex information.
• Effective problem-solving, decision-making, negotiation, and influencing skills.
• Strong verbal and written communication skills; English proficiency is an asset.
• Excellent organizational and time management abilities.
• Proficiency with basic computer applications and electronic data capture (EDC) systems.
• Strong interpersonal skills and the ability to collaborate within a multidisciplinary team

Regards,

Vishnu Das Natesan

dvishnu@radiants.com