Shruti J

Junior Medical Advisor

HBC Lifesciences • Tiempo completo

Aug 2025 - Present • 9 mos

As a Junior Medical Advisor, I support medical affairs and scientific communication initiatives by ensuring accurate, evidence-based, and regulatory-compliant dissemination of pharmaceutical information. Key Responsibilities & Contributions: Conduct comprehensive literature reviews and clinical data analysis Develop and deliver scientific presentations to Medical Representatives (MRs) Create and review LBL (Leave Behind Literature) and Visual Aid materials for drug promotion Validate medico-marketing content for scientific accuracy and regulatory compliance Respond to and resolve medical queries from internal teams and healthcare professionals Design medical questionnaires and scientific assessment tools Participate in and contribute to Continuing Medical Education (CME) programs Provide therapeutic area insights to cross-functional teams Through this role, I have developed strong expertise in medical affairs strategy, scientific content development, medical communication, and pharmaceutical regulatory alignment — skills that directly support my freelance services in medical writing, clinical research, and scientific consulting.

Clinical Trial Assistant

Cliantha Research Organization • Tiempo completo

Dec 2024 - Jul 2025 • 7 mos

As a Clinical Trial Assistant at Cliantha Research Organization, I supported the execution and management of clinical trials in compliance with ICH-GCP guidelines and regulatory standards. Key Responsibilities & Contributions: Assisted in trial documentation management (TMF, ISF, regulatory binders) Coordinated with investigators, sponsors, and CRO teams Supported patient recruitment and screening processes Ensured protocol adherence and regulatory compliance Assisted in SAE/AE documentation and safety reporting Maintained accurate study records and data quality control This role strengthened my expertise in clinical research operations, regulatory documentation, pharmacovigilance support, and Good Clinical Practice (GCP) compliance — skills directly applicable to medical writing, protocol review, and research consultation services.

Clinical Pharmacologist

Zydus Hospital • Tiempo parcial

Jun 2024 - Jun 2025 • 1 yr

As a Clinical Pharmacologist at Zydus Hospital, I contributed to evidence-based patient care by optimizing pharmacotherapy and ensuring medication safety. My role involved reviewing prescriptions, identifying drug interactions, monitoring adverse drug reactions (ADRs), and supporting physicians in rational drug selection. Key Responsibilities & Achievements: Conducted medication therapy reviews to improve treatment outcomes Identified and prevented potential drug-drug interactions Provided evidence-based drug information to healthcare professionals Assisted in antimicrobial stewardship initiatives Monitored and reported adverse drug reactions (pharmacovigilance) Promoted rational and cost-effective prescribing practices