Project coordination, data collection, field level supervision of data collection, qualitative interviewing, development of IEC materials and networking with local communities and health officials. Patient recruitment, follow-up, communication and interaction.
Ph.D Genomics, Bioinformatics, life sciences OR equivalent degree OR MSc, M.Tech Bioinformatics, Human genetics degree from a recognized University or equivalent with at least one research paper in Science Citation Indexed journal.
Masters degree in any branch of Life Sciences with specialization in Clinical Research, Clinical Trials or Clinical Data Management
4 years experience in research and development, industry, laboratory or Science and Technology organizational scientific activities and services
Identify funding opportunities for research activities from external sources. Provide administrative support to researchers for grant submission, activation and execution. Assistance with ensuring statutory compliances for research activities.
Post Graduate Degree in life sciences OR Post Graduate degree in professional course. M.V.Sc, M.Tech, MSc. Degree in Biotechnology Biochemistry, Microbiology, Immunology.
Responsible for supporting preparation of high quality technical documents and reports Responsible for strict adherence to quality standards and regulatory guidelines. Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance. Performs other related duties as required.
M.V.Sc, M.Pharma, M.Sc. Biotechnology, Biochemistry, Zoology, Microbiology with Two years experience for PAT-II. Work experience in the area of Laboratory Animal
M.Sc in any branch of Life Science with at least two years of research experience in Cancer Biology. Masters in Natural or Pharmaceutical Sciences OR Bachelor degree in Engineering or Technology from a recognized University or equivalent.