CR

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.

First Class Post Graduate Degree, including the integrated PG degrees in the field of Life Sciences/Biomedical Sciences /Clinical Research/ Biochemistry/Public Health or related disciplines. Manipal Academy of Higher Education

post-graduate degree in Life Sciences / Biotechnology / Microbiology / Biochemistry / Pharmacology / Clinical Research; Coordinating the informed consent process with the investigators, including consent from legally authorized representatives and re-consent on recovery of capacity

Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.