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Clinical Research Coordinator Jobs in Chennai - Max Neo Clinical Research Services

Clinical Research Coordinator

Max Neo Clinical Research Services
experience-icon 0 Years
salary-icon 12500 - 16600 Monthly
Expired

Posted: 01 Dec 18

Job Description

  • 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

Job Particulars

Role others
Education B.Pharm, M.Pharm, BSc, MSc
Who can apply Freshers
Hiring Process Face to Face Interview, Telephonic Interview
Employment TypeFull Time
Job Id520561
Locality Address
Country India

About Company


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.

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