Dear All, Greetings from Vivo Bio Tech Limited! Job Title: Chartered Accountant (CA) - CRO Industry Experience: 2-5 years Location: Hyderabad Reporting To: Chief Financial Officer (CFO) / Financial Controller MOI: - F2F/Virtual 6-day week Job Title: Chartered Accountant (CA) CRO Industry Location: Corporate Office, Vivo Bio Tech Ltd., Hyderabad Experience: 2 to 5 years Industry: Contract Research Organization (CRO), Preclinical Research Key Responsibilities: Prepare and maintain financial statements in accordance with applicable accounting standards and CRO industry norms. Handle end-to-end accounting operations including accounts payable/receivable, general ledger, and reconciliations. Manage project-based costing, revenue recognition, and budgeting for preclinical studies and CRO contracts. Work closely with the BD and operations teams to evaluate financial feasibility and profitability of client contracts. Liaise with statutory and internal auditors; ensure timely completion of audits and tax filings. Support pricing strategy, bid preparation, and financial modelling for RFPs and new client engagements. Monitor working capital, cash flows, and prepare MIS reports for management review. Ensure compliance with GST, TDS, income tax, FEMA, and other regulatory requirements. Assist in fundraising, investor reporting, and due diligence processes as required. Candidate Profile: Qualified Chartered Accountant (CA). 25 years of relevant experience in the CRO, pharmaceutical, or life sciences industry. Strong knowledge of IND-AS, financial controls, and tax laws applicable to research services. Experience in handling export billing, foreign currency transactions, and government grants (if any). Proficient in Tally ERP, Excel, and financial reporting tools. Good communication and interdepartmental coordination skills. Self-motivated and capable of handling responsibilities independently. Reporting To: Chief Financial Officer (CFO) / Financial Controller Regards, Chandra Kanth | HRD E - chandrakanth.k@virinchi.com
Greetings from Vivo Bio Tech Ltd! Job Responsibility: Study Director Job Title: Scientist/Senior Scientist Company: Vivo Bio Tech Ltd Location: Hyderabad Experience: 4-10 Years Education: Postgraduate (Life Sciences/Pharmacology/Toxicology or related fields) Vivo Bio Tech Ltd is seeking experienced Study Directors to lead and manage Preclinical studies in accordance with GLP and CRO regulatory guidelines . The role involves planning, execution, monitoring, and reporting of the experienced departments below: 1.Toxicology 2.Bio Analytical 3.Analytical Chemistry Job Requirements: Postgraduate degree in Life Sciences or related discipline. 4-10 years of relevant experience in Preclinical with CRO and GLP studies . Strong understanding of regulatory guidelines and data integrity practices. Excellent analytical, communication, and project management skills.
Role Overview: We are seeking a Study Director with proven experience in Safety Pharmacology to lead end-to-end studies in compliance with GLP and regulatory guidelines. The candidate should have prior CRO experience and be fully capable of independently designing study protocols, executing studies, and delivering comprehensive reports to clients. Key Responsibilities: Protocol Design: Develop scientifically sound and regulatory-compliant protocols for CNS, CVS, respiratory safety pharmacology studies, and hERG assay. Study Conduct: Oversee and ensure accurate execution of studies, coordinating with technical staff and laboratory teams. Data Analysis & Interpretation: Review raw data, perform analysis, and draw meaningful conclusions aligned with regulatory requirements. Reporting: Prepare and finalize comprehensive study reports; ensure timely submission to clients. Client Interaction: Act as primary point of contact for sponsors; present study design, interim updates, and final results. Compliance & Quality: Ensure adherence to GLP, ICH S7A/S7B, and OECD guidelines; support audits and regulatory inspections. Desired Profile: PhD / Masters in Pharmacology, Toxicology, or related field. 5+ years of experience in a CRO environment, as Study Director or Principal Investigator. Hands-on expertise in CNS, CVS, respiratory safety pharmacology, and hERG assays. Strong scientific writing and client-facing skills. Ability to independently manage multiple studies from start to finish. Thanks & Regards, G Naga Sravani - HRD