• Know and approve all policies and programs of the organization and oversee their implementation.• Responsible for making decisions on organization issues and board matters. • Represent the organization to the public and serve as a spokesperson.• Keep up-to-date on the business of the organization and responsible for the well-being of this organization.

•Develops and designs clinical protocols for multiple pharma partners that join the adaptive trial platform for support of IND applications and registrations.•Responsible for the design, oversight, and clinical/scientific execution of clinical protocol(s)/program.•Scientific evaluation of new compounds and biomarkers to evaluate drug effectivity in specific mutations within a therapeutic area. •Develops and runs the biomarker translation science committee to evaluate the incorporation of exploratory and enrichment biomarkers.•Reviews, analyzes, interprets, and presents both clinical and translational data both internally and externally.•Writes and/or reviews collaborative abstracts, posters, and content for scientific meetings, conferences, and publications. Supports publication strategy execution, including collaboration with investigators, KOLs, medical affairs, and other internal/external stakeholders. •Presents at investigator meetings and scientific conferences. Develops and delivers clinical and medical affairs trainings, including therapeutic trainings and investigator’s meetings with KOLs. •Leads regulatory submissions (Pre-IND meetings, IND meetings and submission, and study related documents) with the FDA, Health Canada, EMA and NMPA.•Contributes to site study start up activities and delivers CRO and site trainings.•Responsible for the development of clinical protocols, synopses, key manuscripts, abstracts and conference presentations, clinical study reports (CSR), clinical sections of INDs, and other regulatory documents.•Supports the development of real-world evidence clinical studies for post-market approval FDA requirements, as well as the development and execution of landmark clinical studies. •Supports the answering of medical (monitoring) and eligibility queries relating to trial procedures as well as responded to FDA, IRB inquiries. •Supervises the activities of the clinical scientists and members of the clinical science department.

• Supported execution of Phase 2 and 3 clinical trials from pharmaceutical industries as well as investigator-initiated studies and NIH trials following GCP, HIPAA and IRB guidelines.• Co-investigator for mobile stroke unit study and Phase 3 study to evaluate the efficacy and safety of BIIB093 for severe cerebral edema following large hemispheric infarction study (CHARM).• Contributed to the development of investigator-initiated study protocol for evaluation of diagnostic and treatment measures of stroke in young adults• Assisted with development of PI trainings and documentation, regulatory affairs and maintenance of training and delegation logs for various clinical trials.• Contributed to the recording, monitoring and reporting of adverse events in a timely manner.• Assisted with new study startups, site selection and site initiation for various clinical trials; coordinated logistics between the finance team of department of neurology, sponsor and the clinical team.• Gave several presentations about clinical studies in stroke at research retreats, department meetings and conferences. • Worked in close collaboration with physicians, industry sponsors and research staff to perform protocol-specific procedures in neurological trials. • Performed a battery of cognitive testing on patients affected with stroke and had neurological deficits.

• Conducted research work on receptor role in vascular permeability and inflammation in both living specimens (mice) and cell cultures and was responsible for execution of the studies and validation.• Developed protocols and manuscripts for the study in extensive detail and wrote several supportive documents for the research. • Performed data analysis of the results and statistical analysis for interpretation of the data.• Followed standard operating procedures and adhered to accepted research protocols, research regulations and research practices like GCP, which are current and approved.• Participated in interdisciplinary presentations by making poster abstracts, audiovisual presentations and scientific papers.• Developed training for undergraduate student in biomedical sciences. Developed challenging lab work and organized educational and scientific testing material.

• Stabilized traumatic injury patients in the emergency and followed the patients through ICU and hospital stays. • Provided care and education about various useful resources to patients and their families.• Collected extensive patient medical histories and family histories and evaluated patients for physical and mental fitness.• Participated actively in prescreening, tracking and reporting data of patients for different clinical studies.• Gave presentations of medical conditions, active clinical studies and developments in treatment and care. • Collected data, performed procedures, ECGs, and other protocol specific assessments of patients. • Maintained health records, updated prescription records and provided patients with surgical and wound care. • Administered oral medications and injections, scheduled tests and procedures, measured and recorded vitals, and collected of blood samples for various tests and procedures.• Performed emergency procedures like endotracheal intubation, central line insertions, bronchoalveolar and gastric lavages.• Conducted rural health camps for promoting women health and bringing awareness of vaccination for human papilloma virus in school children by collecting Pap smears and providing free vaccinations. • Conducted free eye examinations for school children and prescribed glasses to improve vision.• Conducted free medical camps for people from rural parts of South India which included general examinations, provision of medication and health education to improve hygiene and living conditions.

• Received critically ill patients, stabilized them, and took detailed patient and family history to develop a diagnosis.• Participated actively in prescreening, tracking and reporting data of patients for different clinical studies.• Collected data, performed procedures, and other protocol specific assessments of patients.• Performed emergency procedures like endotracheal intubations, cardiopulmonary resuscitation, central venous lines, arterial lines, bronchoalveolar and gastric lavages.• Gave presentations of medical conditions, active clinical studies and developments in treatment and care.