Navitas Life Sciences Hiring Clinical Research Associate

Navitas Lifesciences pvt ltd; Kolkata District; Sur place; INR 600 000 - 1 000 000; Plein temps

Résumé du poste

Navitas Life Sciences, part of Tech Mahindra, is hiring Clinical Research Associates for Bangalore and other locations including Kolkata. The role involves planning, monitoring, and execution of clinical trials across therapeutic areas, with responsibilities spanning site selection, feasibility studies, TMF maintenance, and regulatory compliance.

The position expects 2–5 years of clinical research experience, strong ICH-GCP knowledge, and excellent communication and coordination skills.

Qualifications

• Graduate degree in Life Sciences (BSc, MSc, BPharm, MPharm, Biotechnology, Nursing).
• 2–5 years of clinical research/clinical trial experience.
• Strong understanding of ICH-GCP guidelines and regulatory requirements.
• Excellent communication, coordination, and organizational skills.

Responsabilités

• Site selection and feasibility studies.
• Plan, conduct, report, and follow up on site monitoring visits.
• Maintain TMF and site-specific files; ensure regulatory compliance.

Connaissances

ICH-GCP

Communication

Coordination

Organizational skills

Formation

Life Sciences degree

Description du poste

Clinical Research Associate – Navitas Life Sciences | Bangalore & Other Locations

Navitas Life Sciences hiring Clinical Research Associates (2–5 yrs) in Bangalore, Delhi, Mumbai, Chennai & Kolkata.

Navitas Life Sciences, a leading global player in clinical development solutions, is expanding its team and inviting applications for the role of Clinical Research Associate (CRA). This is an excellent opportunity for experienced professionals to contribute to world-class clinical trials and be part of a company committed to innovation and healthcare advancement.

Company Overview

Navitas Life Sciences, part of Tech Mahindra, is a trusted partner to top pharmaceutical and biotechnology companies across the globe. With a strong legacy in clinical development, regulatory, and pharmacovigilance solutions, Navitas is known for delivering quality outcomes while ensuring compliance with global regulatory standards.

Job Role & Responsibilities

As a Clinical Research Associate, you will play a pivotal role in the planning, monitoring, and execution of clinical trials across multiple therapeutic areas.

Key Responsibilities:

• Conducting site selection and feasibility studies.
• Planning, preparing, conducting, reporting, and following up on site monitoring visits.
• Procuring, quality checking (QC), and filing essential site documents on time.
• Maintaining the Trial Master File (TMF) and site-specific files.
• Coordinating with project managers and cross-functional teams.
• Ensuring compliance with ICH-GCP, SOPs, and regulatory guidelines.
• Supporting project feasibility reporting and site evaluation processes.

Eligibility / Qualifications

• Education: Graduate degree in Life Sciences (BSc, MSc, B Pharm, M.Pharm, Biotechnology, Nursing).
• Experience: 2 to 5 years of clinical research/clinical trial experience.
• Strong understanding of ICH-GCP guidelines and regulatory requirements.
• Excellent communication, coordination, and organizational skills.

Location & Work Model

• Primary Location: Bangalore (Office-based).
• Other Options: Home-based roles available in Delhi, Mumbai, Chennai, and Kolkata.
• Competitive compensation aligned with industry standards.

Application Process

Interested candidates are encouraged to apply by sharing their updated CV with the HR team at Navitas Life Sciences.

Email: [Provide HR contact if available, else placeholder remains]

Summary Table

• Vacancies: Multiple (CRA positions)
• Required Education: BSc, MSc, B Pharm, M.Pharm, Biotechnology, Nursing
• Experience: 2–5 Years
• Location: Bangalore (Office-based), Delhi, Mumbai, Chennai, Kolkata (Home-based)