Clinical Trial Technology Associate

Airvin Skills; Hyderabad, Chennai, Bengaluru; Presencial; INR 900.000 - 1.300.000; Jornada completa

Descripción de la vacante

Airvin Skills is seeking a Clinical Trial Technology Associate to manage and support our suite of clinical eClinical applications. You will bridge clinical operations and technology to ensure data platforms run smoothly, stay compliant, and support efficient trial execution.

You will configure, maintain, and support EDC, CTMS, and eTMF systems, provide user training, assist with UAT and validations, and ensure adherence to ICH-GCP and 21 CFR Part 11, with attention to GDPR/HIPAA privacy

Formación

• Bachelor's degree in Life Sciences or related field.
• Experience in clinical research operations or data management.
• Familiarity with Medidata Rave, Veeva Vault, or Oracle Clinical.
• Strong analytical and troubleshooting abilities.

Responsabilidades

• System Administration: Configure, maintain, and support core eClinical systems such as EDC, CTMS, and eTMF.
• User Support & Training: Provide troubleshooting, manage access, and train staff.
• Data & Testing: Assist with UAT, integrations, and system validation workflows to ensure data integrity.
• Compliance & Quality: Adhere to ICH-GCP, 21 CFR Part 11, and privacy standards (GDPR/HIPAA).

Conocimientos

Analytical skills

Communication skills

Technical troubleshooting

Attention to detail

Educación

Bachelor's in Life Sciences/Biotech/Microbiology/IT

Herramientas

Medidata Rave

Veeva Vault

Oracle Clinical

Descripción del empleo

Job Overview

We are seeking a detail-oriented Clinical Trial Technology Associate to manage, configure, and support our suite of clinical eClinical applications. In this role, you will bridge the gap between clinical operations and technology, ensuring that critical data platforms run smoothly, remain compliant, and support efficient trial execution.

Key Responsibilities

• System Administration: Configure, maintain, and support core eClinical systems, including EDC, CTMS, and eTMF platforms.
• User Support & Training: Provide technical troubleshooting, manage user access permissions, and deliver system training to internal teams and external site staff.
• Data & Testing: Assist with User Acceptance Testing (UAT), system integrations, and system validation workflows to ensure high data integrity.
• Compliance & Quality: Maintain strict adherence to ICH-GCP guidelines, 21 CFR Part 11, and data privacy standards (GDPR/HIPAA).

Qualifications

• Bachelors degree in Life Sciences, Biotechnology, Microbiology Information Technology, or a related field.
• Prior experience or foundational knowledge in clinical research operations and clinical data management.
• Familiarity with industry-standard software such as Medidata Rave, Veeva Vault, or Oracle Clinical is highly preferred.
• Strong analytical, communication, and technical troubleshooting skills.