Clinical Research Coordinator

KlinEra Global Services

Website: klinera.com
Job details:

Company Description

KlinEra Global Services has been delivering innovative and customized clinical trial and research services since 2005. With expertise in managing Phase 1, 2, and 3 trials, KlinEra provides end-to-end support in clinical trial management, medical monitoring, data management, and site management, ensuring adherence to Good Clinical Practices (GCP). The organization collaborates with leading pharmaceutical, biotech, and medical device companies, especially excelling in trials across therapeutic areas including cardiology, respiratory diseases, infectious diseases, and oncology. KlinEra operates globally with offices in Mumbai, India, and San Jose, CA, USA, bolstering its diverse and client-focused approach.

Role Description

This is a full-time, on-site role for a Clinical Research Coordinator based in Mumbai. Responsibilities include overseeing clinical trials to ensure adherence to protocols, facilitating the informed consent process, coordinating patient enrollment, and maintaining comprehensive documentation. The role also requires close collaboration with investigators and study sponsors to ensure the integrity and quality of research data, as well as compliance with regulatory and ethical standards.

Qualifications

• Experience with Informed Consent and thorough understanding of the process
• Knowledge and application of Protocol and its requirements in clinical research
• Hands-on experience in Clinical Research and conducting Clinical Trials
• Strong organizational, communication, and interpersonal skills
• Attention to detail and ability to adhere to strict ethical and regulatory guidelines
• Bachelor’s degree in Life Sciences, Nursing, or a related field
• Certification in Clinical Research Coordination (preferred but not required)
• Familiarity with Good Clinical Practices (GCP) and ICH guidelines

Location - Parel, Mumbai

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