Clinical Research Coordinator jobs in Chennai at Max Neo Clinical Research Services

The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials.
Coordinating Clinical Trials with Principal Investigators and Research Team
Submission of study protocols to ethics committee for approvals and all pre-study documentation requirements
Assist Principal Investigator in patient selection and enrollment in clinical trials.
Investigational Product accountability and dispensing
Scheduling patient visits and follow up
Case Report Form Completion
Assuring adequate reporting of adverse events
Ensuring that collection of data from medical records, subject interviews, questionnaires, diagnostic tests and other sources are complete and reported accurately
Maintain study files on an ongoing basis to ensure that the files are complete and can be used as a source of reference.
Maintaining communication and correspondence with subjects, sponsor, monitor and other site study personnel

Max Neo CR services is based in Chennai, India, offering clinical research Phase II -- Phase IV, BA/BE studies, Medical writing services to the Pharmaceutical, Nutraceuticals and Cosmetics Industries.

Our Collaborative approach and extensive partnership allow us to understand needs, share ideas, and leverage resources to the benefit of our client.

Max Neo CRS is uniquely placed to help you design, develop and implement clinical trial solutions that meet your specific needs, Our aim is to help optimize your clinical timelines and support regulatory submissions to bring your product to market quickly and safely.

As per ICH GCP and Other regulatory standards as per sponsor's requirements.

Our highly experienced, locally based teams allow us to deliver flexible and innovative solutions to accessing patient populations, and ensuring that our clinical trials make and impact for sponsors, clinicians and patients.