Health Care

Description-Graduates/ Postgraduates in with 1 to 3 years of working experience in building and reviewing study based on specifications may apply. Experience in creating paper or eCRF using Framework, Adobe Acrobat or Microsoft Word or EDC/RDC tools (OC, RAVE) and working knowledge in study database building and validations in EDC/ RDC/ CDM tools is mandatory.

Required Qualifications:Graduates/ Postgraduates in Life Sciences/ engineering/ computer applications. Required Experience: 1+ YEARS experience in Clinical SAS. candidates from Clinical data management who are Oracle programmers and PLSQL.Our client, a global clinical research organization offering cost-effective and time-sensitive solutions for conducting clinical studies have the following requirements

Research QA experience of clinical trial in phase I to phase IV clinical trials. Hands on experience of GCP auditing. In-depth understanding of GCP guidelines from ICH, NCI. Responsible for on site clinical trial audits of phase II and III, global multicentric,clinical trials. Responsible for identification and preparation of SOPs which are missing in the system. Responsible for periodic review, distribution, maintenance, withdrawal and archiving of SOPs.

The project manager will head a team of medical content researchers and medical writers. The team will be assigned CME and Content projects that have been entrusted to the company. He/ She will co ordinate and contribute to the team activities in maintaining quality of project and adhering to time lines. He/ She will also be co ordinating with senior specialist in all specialties, Medical associations and pharmaceutical companies on various CME and Content projects.