B.Pharm

Analyze genomic and clinical datasets to assist in patient stratification and predictive modeling. Assist in creating documentation, presentations, and technical reports summarizing insights and results.

Good English communication skills. Good skills in reading handwritten Notes, Doctors prescription. Basic knowledge of medical terms and terminologies. Basic knowledge of Computer. A Global Phase 3, Double Blinded And Placebo- Controlled Study Evaluating The Efficacy And Safety of Etavopivat In Adolescents And Adults With Sickle Cell Disease.

Bharat Biotech International Limited is an Indian multinational biotechnology company headquartered in the city of Hyderabad, India engaged in the drug discovery, drug development, manufacture of vaccines, bio-therapeutics, pharmaceuticals and health care products.

Should have knowledge of country specific dossier preparation. Should have knowledge of country specific dossier preparation

Professional having B.Pharm, BAMS, B-Tech, MPH. Preference will be given to professionals having experience in Digital Health. Foster partnerships with academia, industry, and international organization to accelerate digital health adoption.

A Diploma in Pharmacy, Bachelor of Pharmacy. Must have registered with Pharmacy Council and must keep the registration alive by renewing it regularly every year.

BPharm, BSc, MPharm, MSc, MBBS, BAMS; Experience in PV/ Clinical Research drug safety preferred. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.

TCS combines tech expertise and business intelligence to catalyze change and deliver results. Our mission is to help customers achieve their business objectives by providing innovative, best-in-class consulting, IT solutions and services and to make it a joy for all stakeholders to work with us. Clinical Data, Regulatory, Clinical Operations, Pharmacovigilance; Should be open to work In shifts

Expertise in designing, executing, and reviewing cleaning validation protocols. ensuring compliance with cGMP. EMA. and other global regulatory requirements. Specializing in stability studies, regulatory compliance, and quality assurance oversight. Managing stability programs in alignment with ICH guidelines