MD

Develop study protocols, standard operating procedures, and other essential documents in line with regulatory guidelines. Oversee the implementation of study activities, ensuring adherence to timelines, quality standards, and Good Clinical Practice guidelines. 

MBBS, Doctor of Pharmacy, M.Sc. Statistics, M.Sc. in Life Sciences with 2 years of experience in the field of systematic reviews, network meta-analysis is mandatory.

Ph.D, MD, MS, MDS or equivalent degree OR three years of research, teaching, design and development after MVSc, M.Pharm, M.E, M.Tech with at least tree research papers in high impact Journals.

Professionals having proven competency and success in their area of specialization, with at least 10 years of post- qualification experience and should possess minimum M.Sc, B.Tech, BE, MCA, MPH, B.Pharm, BSMS, MD in AYUSH.

Masters, Integrated Masters Degree in Pharmaceutical Sciences or Natural or Agricultural OR bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent.

Develop, strategize and plan business activities like portfolio selection, brand planning and launch, KOL management, compliance and other crucial activities in therapy and additional therapeutic areas. This is towards assimilation of scientific and medical know-how in aligning activities to meet the business goal of the concerned therapeutic areas, business unit. Understand on ground clinical practices by interacting with clinicians, to develop practical knowledge and utilize it to provide closer-to-market product solutions

As a Principal Medical Writer you will play a pivotal role in leading the Medical Writing efforts for Marketed Products and Lifecycle Management, both globally and at regional, local levels. You will represent the department as a subject-matter expert on clinical study teams, leading document-related meetings and reviewing study-related documents.

Construction of therapeutic cells with synthetic circuits targeting relapse in B-cell Acute Lymphoblastic Leukemia. Development of a CRISPR-Cas9 based AAV vector for HDR Homology Directed Repair mediated genetic correction as a therapeutic intervention for Gauchers disease

handle R&D projects independently in the areas of epidemiology, big data analytics, drug/ target/ biomarker discovery, preclinical and clinical evaluation of medical devices, IVDs, therapies, vaccines, field feasibility studies of the novel interventions, and experience/ exposure to regulatory aspects of health technologies, IP protection, Technology transfer. Health policy development and implementation. MD, MS or equivalent degree recognised by MCI, NMC OR MBBS or equivalent degree recognized by MCI, NMC, with MPH from a recognised university OR M.Sc or MBBS or equivalent degree, recognised by MCI, NMC, with Ph.D. from a recognised University.