Jd ptb qm 2018 revised

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CLINICAL DEVELOPMENT SERVICES AGENCY An extra mural unit of THSTI, Department of Biotechnology, Ministry of Science & Technology, Govt. of India 3rd Floor, THSTI Building, 3rd Milestone, Gurgaon-Faridabad Expressway, Faridabad – 121001 (Haryana) Recruitment Notice No. CDS/RN/08/QM-PTB/2018

Name of the post /

Quality Manager (Preterm Birth Program)

Emoluments/ Duration

Up to Rs. 55,000 per month, consolidated upto December 2018 likely to be continued Gurgaon Civil Hospital, Gurgaon Oversees quality management processes and provides guidance and support to project teams to meet quality standards.

Location Job profile

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Qualifications Experience

Skills

Ensure that assigned study is conducted in accordance with study protocols, GCP guidelines, and applicable regulatory requirements. Lead or assist with identifying non-conformances with requirements, provide suitable recommendations and facilitate ongoing quality improvements. Proactively identify the project risks and assist in providing training to study staff in good clinical and documentation practices. Maintain GCP compliant processes which control the quality of work at the study site Oversee/Conduct source document verification and case record forms for assessing the study trends Overseeing and/or performing quality functions and executing quality programs (clinical operations, clinical laboratory, data management review) Collaborate with clinical and project management team to ensure compliance with quality standards, timelines and appropriate follow-up in areas of deficiency Coordinate expert monitoring visit/ audits as per project requirement. Work with Clinical Portfolio Management and other internal departments on their requirements as and when required Actively lead or assist activities in the areas of Internal Quality improvements and CAPA (Corrective and Preventive Actions) Manage team of study monitors Guide and mentor the study monitors for project deliverables

Master’s degree in life sciences or biomedical sciences or pharmacy or Public and Health or Clinical Research. 4-5 years of demonstrated experience in the area of clinical research project management, Clinical operations, clinical research monitoring and team management. GCP trained and experience of handling observational studies will be preferred.  Good understanding of needs for project and job responsibilities.  Extensive knowledge of GCP, observational studies and appropriate regulations and guidelines.  Ability to develop and implement clinical monitoring plans, SOPs, database concepts, and formats


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Jd ptb qm 2018 revised by BioTecNika - Issuu