Clinovo hiring Clinical Research Associates

Clinical Research Associate Openings – Clinovo India

Clinovo hiring experienced Clinical Research Associates (2–3 yrs) across Mumbai, Delhi, Bangalore, Chennai, Kolkata & Pune.

Clinovo is expanding its Clinical Operations team and hiring experienced Clinical Research Associates (CRAs) across multiple metro locations in India. This opportunity is ideal for candidates who have hands-on monitoring experience, strong ICH-GCP knowledge, and the ability to manage clinical sites with accuracy and discipline.

Company Overview

Clinovo is a global clinical research solutions provider offering end-to-end support across clinical operations, data management, regulatory services, and digital trial enablement. With a strong presence in India and international markets, Clinovo partners with leading pharma, biotech, and CRO clients. The organisation maintains high operational standards aligned with ICH-GCP, ethical guidelines, and industry best practices.

Job Role & Responsibilities

Clinical Research Associate (CRA)

• Conduct site selection, site initiation, routine monitoring, and close-out visits.
• Perform monitoring activities as per ICH-GCP, SOPs, and study protocol.
• Track subject recruitment and support site-level enrollment strategies.
• Deliver protocol training and maintain continuous communication with site teams.
• Ensure regulatory compliance, data accuracy, timely CRF completion, and documentation control.
• Manage submissions, approvals, enrollment updates, and resolution of data queries.
• Maintain and verify essential documents within the Trial Master File (TMF) and Investigator Site File (ISF).
• Prepare monitoring reports, follow-up letters, and other required documents.
• Collaborate closely with clinical trial managers and cross-functional stakeholders.

Eligibility / Qualifications

• Education: Bachelor’s degree in Life Sciences or Healthcare domains.
• Experience: Mandatory 2–3 years of on-site monitoring experience.
• Skills Required:
  • Strong understanding of ICH-GCP and clinical trial regulations.
  • Knowledge of therapeutic areas and protocol requirements.
  • Proficiency in MS Word, Excel, and PowerPoint.
  • Strong communication, organization, and problem-solving skills.
  • Ability to build strong site relationships and support study-level operations.

Relevant courses (comma-separated): B.Sc Life Sciences, B.Pharm, M.Pharm, B.Sc Nursing, M.Sc Clinical Research, PG Diploma in Clinical Research, Certificate in ICH-GCP, Certificate in Pharmacovigilance.

Location & Salary

• Locations: Mumbai, Delhi, Bangalore, Chennai, Kolkata, Pune
• Salary: Based on experience and internal evaluation.
• Work Mode: Work from office; on-site monitoring required.

Application Process

Interested candidates may share their updated CV to:
yuvakiran.beesetti@clinovo.com

Use subject line: Application – Clinical Research Associate

FAQs

1. Is on-site monitoring experience mandatory?
Yes. Only candidates with 2–3 years of CRA experience will be considered.

2. Is this a remote role?
No. This role requires office-based work plus on-site visits.

3. Are multiple locations available?
Yes—six metro locations across India.

4. What documents should applicants prepare?
Updated CV, certifications (ICH-GCP), experience letters, and ID proof.

5. Are freshers eligible?
No. Only experienced CRAs can apply.

Summary Table