Clinical Trial Project Manager Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trials with quality, on time, and within scope and budget. Leverage scientific and regulatory knowledge to prepare and/or provide technical consultation for clinical and regulatory documents, prepare for meetings with regulatory agencies

Seeking a dynamic independent and experienced Research Associate in Clinical Management for processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. Ensuring accurate, timely, and consistent data reaches the clinical teams and other groups. Master degree in pharmacy/ life science/Biology/Biotechnology/ Biochemistry/Diploma in Clinical Research

Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system.

The recruited candidate will perform majority of experiments proposed in the study, which includes preparation and characterization of nanoparticles, in vitro and in vivo safety and efficacy analysis etc. The Project Research Scientist-I will also take care of consumables ordering, storage and maintenance. The candidates with M.Sc., qualification shall enrol for Ph.D programme.

Postgraduate degree including the integrated PG degree in any branch of Life Sciences - Biological Sciences, Biotechnology, Biochemistry, Genetics.

Provide technical inputs on review of CMC data for Central CDSCO and State dossiers related to new products under development Liaison with other departments such as l&D, Quality, Supply chain, Project Management, etc to deliver high quality dossiers, in accordance with business priorities

You will be executing the Product Management Teams marketing strategy, analysing market trends, consulting with doctors on new product potential, and relaying feedback to the Product Management Team. Additionally, responsibilities include identifying key opinion leaders, monitoring product availability, and implementing brand strategies to facilitate a successful product launch.

Graduate of minimum three years duration in pharmacy with three years experience in pharmacy OR Post graduate degree in Pharmacy. Neonatal and or Pediatric Nursing experience, Working Knowledge of Data Entry in the computers Experience in drug preparation in clinical research study preferably involving children or neonates.

Membrane preparation and characterization. Prior experience of working in research laboratory, industry desired. Direct Sea Water Electrolysis by electrolyte engineering & by coupling electrolyser directly with FO module.

Establish a Drug Metabolomics Laboratory for North Eastern States. Master degree in Pharmaceutical or Natural Science with first class.

D.Pharm, Integrated Pharmacy course Certificates issued by Govt of Tamil Nadu Only.

Candidates with research experience in tumor immunology, cancer biology with a proven hand in animal handling, animal animal-related experiments as evident from the original research publications will be preferred.

2 years of experience of working in a molecular diagnostic laboratory for candidates with M.Sc, B.Tech in the above subjects. 1 year experience for candidates with Phd in the above subjects. Candidates with experience of working in a molecular diagnostic laboratory or accredited labs or those labs who have applied for accreditation will be preferred.

If the number of JRF and INSPIRE qualified candidates are large, selection will be based on interview of the JRF and INSPIRE qualified candidates only. The selected candidates will be registered for BRIC-DBT-RCB-Ph.D programme and he/she can be placed in any centres of the IBSD

Support in incubation activities and manage various schemes of the Incubator. Manage and guide on Biosafety and ethics approvals for the incubatees. Manage contracts, tendering arrangements and ongoing relationships with incubates, agencies and vendors. 

Biophore, an established pharmaceutical company, is engaged in the development and manufacturing of niche pharmaceutical products for the generic industry.

D.Pharm or equivalent course approved by paramedical council. Pharmacy council Registration. Application are invited for the posts mentioned below in State/District Health and Family Welfare Society, National Rural Health Mission.

Doctoral degree in Science, Engineering, Technology, Pharma, MD, MS from a recognized University or equivalent and experience in Research and Development in industrial and Academic institutions or science and technology organizations and scientific activities and services. To operate and maintain analytical and/or imaging Equipment such as Ion Chromatograph/ HRMS/ IRMS/ NMR/ photoacoustic imaging/confocal laser scanning microscopy/ ICPMS or related equipment and in interpreting their data.

Adult stem cell derived exosomes, A cell-free therapy for glaucoma. Experience in animal models for evaluating preclinical safety, pharmacokinetics and efficacy will be preferable. Candidates with GPAT or equivalent exams will be given a preference. Candidate must be interested in learning new concepts, tools, and techniques.