Rohit T. Email and Phone Number

Provides superior quality innovative products and services that inspire costumer recommendations. Responsible for developing, implementing and executing strategic plans for organization (or lines of business and brands within organization) in order to attract potential customers and retain existing ones. Undertake daily administrative tasks to ensure the functionality and coordination of the department’s activities. Communicate directly with clients and encourage trusting relationships

Activities: Technical guidance and Assistance for:(a) Small business start-up (b) Independent Film makersProjects:(a) Writing Documentation, Quality, Supplier and Co-manufacture Expectation, Procedure, SOP, Product Master file Manuals for Greenly FPO a Farmer Producer organization base in Siliguri, Darjeeling, West Bengal. Nov, 2019 to present.(b) Composer and Sound designer for Short film “Samarpit” by Sangita Motion Pictures. Director Kondaiah Mane. From April, 2019 to June, 2019.(c) Film “Jungle mai mor – Ode to the unknown” by Nishanthi Evani as Sound designer. From March, 2019 to April, 2019.(d) Composer and contributor for “Journeys of a Skeleton – Beacon of tolerance” initiative by Alex Sebastian and Jerry Marrota. From Jan, 2019 to March, 2019.(e) Film Rude Dog Trailer by Roger Slagle as Music composer, Sound editor and technical assistance. From Oct, 2018 to Dec, 2018.(f) Film DIVIA by Roger Slagle as music composer, Sound editor and technical assistance for cost cuttings From Nov, 2014 to Dec, 2017.(g) Assisted Johari Digital Healthcare Ltd, Jodhpur (Rajasthan) as Asst. Marketing Manager From Nov, 2017 to Dec, 2017. Developed, implemented and executed strategic marketing plans for organization and lines of business and brands within organization in order to attract potential customers and retain existing ones. Support marketing and sales executives in organizing various projects. Assist in the organizing of promotional events and traditional or digital campaigns and attend them to facilitate their success. Prepare and deliver promotional presentations.(h)

Provided technical support to Investigator Site, CRA, and Client (Sponsor) in two way business environment with applicable Good Clinical Practice Guidelines and SOPs.Investigate problems and run sample management reports related with Clinical Study Protocol requirements including collection, shipping, and testing.Generate, resolve and track queries to address problematic data identified during data review activities and apply proper major or minor modification / correction to the database.Notified Lab Panics, Lab Alerts, Exclusions and Toxicity levels to protocol designated parties, Investigators, and Clinical Monitor and sponsors as per Study protocol and Standard Operating Procedures.Coordinating storage and shipment of samples based on protocol specifications.Track samples and chronology of data by generating reports.

M.Sc in Clinical Research Management + PGDPBM with 100% scholarship (AVIVA Young Scholar 2009 – ICRI | CNN IBN)Education in M.Sc in Clinical Research Management• Principles of ICH-GCP Guidelines.• Good Manufacturing Practices• FDA’s Code of Federal Regulations.• Six Sigma Standards (DMAIC & DMADV)• Pharmacovigilance.• Informed Consent Process• Intellectual Property Rights, Copyrights, Patents, Trademarks.• Methods of Data Entry and Data Migration.• Clinical Data Management processes Safety• Data Management, SAE Reporting and Reconciliation.• Data Cleaning and Validation.• Discrepancy Management and Query Management• Methods of Data Entry and Data Migration.• Medical Coding & Thesaurus Management System (MedDRA, WHODD, COSTART, ICD9CM, WHOART).• Pharmacology (Pharmacokinetics and Pharmacodynamics).• Clinical Data Interchange Standards Consortium (CDISC).• Audits and inspections in Clinical Research.• Planning and Designing a Study• Creating DVGs, Questions, Question groups, DCMs and DCIs as a part of designing Case Report Forms (CRFs) in Oracle Clinical• Test Data Entry – Initial Login, First and second pass data entry and Key changesEducation in PGDPBM: Post-Graduate Diploma in Pharma Business Management.• Marketing Management• Human Resources Management• Project Management• Operation Management - Sales and Distribution Management• Intellectual Property Rights• Business Communication• International Business and Marketing.• Product and Brand Management

• Manual Adjudication of Claims filed by different Physician in US.• Mentoring new recruited team members in Adjudication process.• Explaining different aspect of HIPAA and US FDA Code of Federal Regulations.• Correspondence with different department, Reporting and Creating presentations and lecture content.• Perform other duties as assigned by management.