Clinical Research Job at Emmes India | Bachelor’s in Life Sciences Required – Apply Now!
Are you ready to step into a dynamic role that directly impacts global health and medical innovation? Emmes, a leader in clinical research for over 47 years, is offering a full-time opportunity based in India (Bengaluru, Ahmedabad, New Delhi, or remote) for professionals with a bachelor’s degree in a scientific field and hands-on experience in clinical site monitoring. If you’re passionate about improving lives through research and compliance, this opportunity might be exactly what you’ve been waiting for.
About the Company:
Emmes Group is a global contract research organization (CRO) with a legacy of over 47 years in delivering excellence in clinical research. From public-private partnerships to advanced trials in cell and gene therapy, neuroscience, infectious diseases, and ophthalmology, Emmes is at the forefront of medical innovation. With a culture rooted in collaboration, ethics, and patient-centricity, Emmes offers a platform for passionate professionals to grow and contribute meaningfully.
Job Title: Clinical Research Associate II
Location: India – Bengaluru
Department: Clinical Operations
Employment Type: Regular Full-Time
Job Code: 2414
Primary Purpose
The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either onsite
or remotely to ensure trials are conducted in compliance with protocols and regulations.Responsibilities of Clinical Research Job
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Schedule and conduct on-site and remote monitoring visits
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Review informed consent forms, source documents, adverse event tracking, and investigational product storage
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Ensure protocol compliance and regulatory documentation integrity
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Provide training to site staff on GCP, protocol specifics, and documentation
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Participate in audits, site closeouts, and investigator meetings
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Communicate with site personnel to resolve study issues and maintain site performance
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Assist with study documentation, ethics submissions, and recruitment strategies
Qualifications of Clinical Research Job
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Bachelor’s degree in a scientific discipline (life sciences preferred)
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1–2 years of monitoring experience (remote or on-site)
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Strong knowledge of ICH-GCP guidelines and clinical operations
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Excellent attention to detail, organization, and communication skills
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Comfortable with MS Office and remote project collaboration tools
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Ability to multitask, problem-solve, and manage time independently
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Willingness to collaborate with internal and external stakeholders
Keywords: Clinical Research Associate, CRA, Clinical Operations, Monitoring, Clinical Trials, Compliance, Protocol, Regulations, MS Office Suite, Communication Skills, Problem-Solving
