Pharmacy

Seeking an experienced Site Manager - Clinical Trials to lead and oversee end-to- end clinical trial execution and site administration. The ideal candidate will be responsible for ensuring regulatory compliance, operational excellence, staff management, sponsor/CRO coordination, and smooth day-to-day site functioning across multiple studies.

PhD in Veterinary, Clinical Biochemistry, Chemistry, Nanotechnology, Chemical Engineering, Biomedical Engineering, Pharmaceutical Sciences, Material Sciences, etc.

Masters Degree in Pharmacology/ Physiology/ Veterinary Science/ Pharmacy/ Botany/ Chemistry/ Pharma Chemistry/ Biochemistry / Microbiology of a recognized University or equivalent.

Master degree in Pharmacy, Clinical Pharmacology, Pharmacy Practice, and Clinical Research. OR Pharm.D / MBBS / BDS from a recognised university/Institute.

An eminent scholar having a Ph.D. degree in the concerned/allied/relevant discipline, and published work of high quality, actively engaged in research with evidence of published work

To develop promotional content and manage label updates in alignment with brand and regulatory requirements and ensure delivery of high-quality, compliant, and impactful content across multiple channels.

Actively leads product registrations by preparing / requesting documentation needed for complex filings. Employs project management skills to monitor activities and meet deadlines.

Identify, engage and onboard high-quality vaccinating clinics and specialist practices across Hyderabad and surrounding areas. - Build and maintain trusted relationships with dermatologists, consulting physicians, pulmonologists, rheumatologists, infectious disease specialists, transplant surgeons and other relevant clinicians. 

An initiation Clinical Research Associate (iCRA) specializing in Pre SIV and Activation tasks will be assigned & accountable for managing and driving the strategy for the startup, Pre SIV and Activation tasks of the study. The iCRA also supports submission and approval process for the protocol amendments if applicable.