Clinical Research Assistant

Airvin Skills; Hyderabad, Chennai, Bengaluru; Presencial; INR 300.000 - 500.000; Jornada completa

Descripción de la vacante

Airvin Skills in Hyderabad (India) is seeking a Clinical Research Assistant to support planning, execution, and documentation of clinical studies under supervision. Responsibilities include data entry, regulatory filing, consent processes, and coordinating lab logistics within GCP-compliant frameworks.

The role emphasizes attention to detail, organization, and clear communication with study teams, sites, and sponsors. Fresh graduates with life sciences backgrounds are welcome to apply.

Formación

• Bachelor's degree or equivalent in life sciences, pharmacy, nursing, or related field.
• 0–2 years of clinical research experience; freshers may be considered.
• GCP knowledge and understanding of clinical trial processes.
• Strong attention to detail and good communication and organizational skills.
• Proficiency in MS Office and basic data entry tools.

Responsabilidades

• Assist with participant recruitment, screening, and scheduling.
• Collect, enter, and verify study data in CRFs or electronic systems.
• Maintain study files and regulatory documents.
• Support informed consent processes and documentation.
• Help prepare samples and coordinate lab logistics.
• Report adverse events and deviations to the team.
• Ensure compliance with GCP, ICH, and ethics requirements.
• Assist audits and ethics submissions.

Conocimientos

Attention to detail

Organization

Communication skills

MS Office proficiency

Educación

Bachelor's degree in life sciences, pharmacy, nursing, or a related field

Descripción del empleo

Summary

The Clinical Research Assistant supports the planning, execution, and documentation of clinical studies, working under the guidance of the Principal Investigator and Clinical Research Coordinator to ensure studies run smoothly and comply with protocols and regulations.

Key Responsibilities

• Assist with participant recruitment, screening, and scheduling
• Collect, enter, and verify study data accurately in case report forms (CRFs) or electronic data capture systems
• Maintain study files, regulatory documents, and investigator site files
• Support informed consent processes and ensure documentation is complete
• Help prepare samples, process specimens, and coordinate lab logistics
• Report adverse events and protocol deviations to the study team
• Ensure compliance with GCP, ICH guidelines, and institutional/ethics committee requirements
• Assist with preparing for audits, monitoring visits, and ethics submissions

Qualifications

• Bachelors degree in life sciences, pharmacy, nursing, or a related field
• 0–2 years of experience in clinical research (freshers may be considered)
• Knowledge of GCP and clinical trial processes
• Strong attention to detail, organization, and communication skills
• Proficiency in MS Office and basic data entry tools

Preferred

• GCP certification
• Prior exposure to a hospital or CRO setting