CLINICAL RESEARCH ASSOCIATE

Lusynco; Ahmedabad District; On-site; INR 373,000 - 734,000; Full time

Benefits offered by this job

Health insurance

Job summary

Refined Reports Data in Ahmedabad is seeking a Clinical Research Associate for in-person work. You will handle trial setup, site management, IP materials, and inventory checks to ensure protocol adherence.

The role requires extensive travel and a Bachelor’s in biological sciences; familiarity with FDA regulations, SOPs, and ICH-GCP is essential. Health insurance is included as a benefit.

Qualifications

• Education: Bachelor's degree in biological science or related field.
• Understanding of the pharmaceutical industry, terminology, practices, and FDA regulations/practical implementation.
• Travel availability to travel extensively and on short notice.

Responsibilities

• Trial setup & management: write trial protocols, identify/evaluate/close trial sites, order and track IP materials, and conduct inventory reconciliation.
• Site supervision & training: train site staff on therapeutic areas and documentation, conduct regular site visits, coordinate meetings, and write visit reports.
• Ethics & regulatory compliance: liaise with ethics committees and regulatory authorities, ensuring strict adherence to SOPs, local regulations, and ICH-GCP guidelines.
• Patient & data care: protect subject confidentiality and verify proper IP dispensing/administration according to protocol.

Skills

Verbal communication

Written communication

Workload management

Education

Bachelor's degree in biological science or related field

Tools

MS Word

Excel

PowerPoint

Job description

Clinical Research AssociateRefined Reports Datais hiring aClinical Research Associatefor in-person work in Ahmedabad.
Key Details- Company:Refined Reports Data

• Location:Ahmedabad, Gujarat
• Employment Type:Full-time, Permanent, Fresher
• Pay:₹3,72,572.86 – ₹7,33,555.00 per year
  Requirements- Education:Bachelor’s degree in biological science or a related field.
• Knowledge:Understanding of the pharmaceutical industry, terminology, practices, and FDA regulations/practical implementation.
• Skills:Strong verbal/written communication, computer proficiency (MS Word, Excel, PowerPoint), and workload management skills.
• Travel:Ability and availability to travel extensively and on short notice.
  Responsibilities- Trial Setup & Management:Write trial protocols, identify/evaluate/close trial sites, order and track investigational product (IP) materials, and conduct inventory reconciliation.
• Site Supervision & Training:Train site staff on therapeutic areas and documentation, conduct regular site visits, coordinate meetings, and write visit reports.
• Ethics & Regulatory Compliance:Liaise with ethics committees and regulatory authorities, ensuring strict adherence to SOPs, local regulations, and ICH-GCP guidelines.
• Patient & Data Care:Protect subject confidentiality and verify proper IP dispensing/administration according to protocol.
  Benefits- Health insurance