CR

Responsible for developing, establishing and maintaining QA procedures related to clinical trials to ensure compliance with applicable regulatory guidelines.

Preferred knowledge of other related disciplines e.g. clinical, regulatory affairs, clinical statistics relevant to aggregate report writing and clinical development 

Degree with life Science background, trained in Clinical research e.g. Diploma in clinical research , or MSC Clinical research and PharmD

B.Sc. Life Science / B. Pharm with Post Graduate Diploma in Clinical Research Or M.Sc. in Life Science/ M. Pharm with PG Diploma in Clinical Research. TATA MEMORIAL CENTRE

B.Sc. Life Science / B.Pharm with Post Graduate Diploma in Clinical Research Or M.Sc. in Life Science/ M. Pharm with PG Diploma in Clinical Research. TATA MEMORIAL CENTRE

BSc. Life Science / B.Pharm with Post Graduate Diploma in Clinical Research (PGDCR). The activities include assisting PI/Co-I with screening of trial participants, documentation of IC process, ensuring Protocol compliance, IEC communication, data management, maintaining Investigator Study File, processing of participant reimbursements maintenance of study related trackers/ logs etc.

Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.

Postgraduate degree in a Life Sciences / Health Sciences / Public Health / Clinical Research with post-qualification experience OR PhD. clinical research/RCT coordination, GCP, data management, regulatory documentation and transplant/infectious-diseases research 

Homi Bhabha Cancer Hospital & Research Centre, Aganampudi, Visakhapatnam recruitment; Graduate in Science E.g. B.Pharm, Life science, B.Sc., Biotech, Zoology, Botany, etc., with PG Diploma in Clinical Research is preferable.