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
Dear All, Greetings from Vivo Bio Tech Limited! Job Title: Trainee System Administrator/System Administrator Experience: Fresher Location: Banjara Hills/Pregnapur - Hyderabad MOI: - F2F 6-day week - Alternate Saturdays Week Off Office Timings - 9 AM to 5 PM Designation: Trainee System Administrator Years of Exp : Freshers Location: Hyderabad Positions - 2 Roles and Responsibilities: Good to have Documentation Experience (Added Advantage) Configuring and maintaining the networked computer system, including hardware, system software, and applications Ensuring data is stored securely and backed up regularly Diagnosing and resolving hardware, software, networking, and system issues when they arise Replacing and upgrading defective or outdated components when necessary Monitoring system performance to ensure everything runs smoothly and securely Working Location: Vivo Bio Tech Ltd Survey # 349/A, Pregnapur Village, Gajwel Mandal. Siddipet District, PIN 502311, Telangana, India. or Virinchi Limited Above ICICI Bank, Beside Bajaj Electronics, Illiyas Mohamed Building, 5th Floor Road No. 1, Banjara Hills, Hyderabad. Regards, G Naga Sravani - HRD nagasravani.g@virinchi.com
Job Title : Veterinarian for Preclinical research organisation Location: Pregnapur, Hyderabad Experience : Freshers Reports To : Head Preclinical Research / Study Director / TFM Job Summary: We are seeking a qualified and experienced Veterinarian to support preclinical research programs within a GLP-compliant Contract Research Organization environment. The veterinarian will be responsible for the care, welfare, and regulatory compliance of laboratory animals used in safety, pharmacology, and toxicology studies, ensuring adherence to OECD GLP guidelines and sponsor requirements. Key Responsibilities: Animal Care & Welfare Oversee the health and welfare of laboratory animals (rodents, rabbits, dogs, non-human primates, etc., depending on facility scope). Conduct daily health observations, physical examinations, and maintain detailed medical records. Provide preventive and therapeutic veterinary care in accordance with GLP guidelines. Research Support Work closely with study directors, toxicologists, and animal facility staff to support preclinical studies. Participate in study design discussions to ensure compliance with GLP and animal welfare regulations. Administer test compounds (oral, intravenous, subcutaneous, etc.) and collect biological samples (blood, urine, tissues). Support surgical and anesthesia procedures where required. Regulatory Compliance Assist in preparing and reviewing study protocols, SOPs, and reports for GLP compliance. Support inspections and audits from regulatory authorities and accreditation bodies. Documentation Maintain accurate and complete veterinary records in compliance with GLP principles. Prepare health status reports, necropsy reports, and incident documentation. Qualifications Education: Bachelors in Veterinary Science & Animal Husbandry (B.V.Sc & A.H.), with registration from Veterinary Council of India (VCI). Masters degree in Veterinary Regards, G NagaSravani-|HRD nagasravani.g@virinchi.com Vivo Bio Tech Ltd., Vivo Bio Science Park, Pregnapur Village, Gajwel Mandal. Siddipet District, Hyderabad, Telangana, India. Website : www.vivobio.com
Job Position: Study Director Location: Pragnapur, Hyderabad Company: Vivo Bio Tech Ltd Job Role: The Bioanalytical Associate role focuses on supporting in-vitro ADME studies and plasma sample analysis in preclinical drug development. The successful candidate will be integral in analyzing and interpreting bioanalytical data to support early-stage drug discovery efforts. Responsibilities Conduct routine ADME assays, such as protein binding and metabolic stability, to generate key data supporting drug development decisions. Prepare and analyze plasma samples for pharmacokinetic studies, including the measurement of drug concentration, metabolite profiling, and related biomarkers. Analyze data sets, provide scientific interpretation, and communicate results to cross-functional teams in a clear and concise manner. Maintain concise and accurate records of all study activities in accordance with industry guidelines and company policies. Troubleshoot assay issues, propose corrective actions, and implement process improvements to enhance the efficiency and reliability of bioanalytical data. Assist in the coordination of outsourced research studies or other tasks assigned by management. Requirements Bachelors degree in Analytical Chemistry, Biochemistry, or a related field. 5+ years of hands-on lab experience in bioanalysis, with a focus on ADME/PK studies and plasma sample analysis. Hands-on lab experience with ADME screening assays, such as protein binding and microsomal stability. Experience with plasma sample bioanalysis in support of non-clinical pharmacokinetic studies. Experience with LC-MS/MS, HPLC, UPLC, and related analytical techniques for the quantification and characterization of drug candidates in biological samples. Strong analytical and troubleshooting skills with the ability to interpret complex datasets. Nice-to-haves Familiarity with drug discovery and development, especially within preclinical research. Experience with quantitative LC-MS/MS bioanalytical techniques and ABSciex mass spectrometers. Knowledge of relevant bioanalytical software (e.g., Analyst, Prism). Thanks & Regards G NagaSravani|HRD nagasravani.g@virinchi.com