Company Description AlzaSyno Life Sciences offers a comprehensive suite of CRO (Contract Research Organization) services tailored to the pharmaceutical, bio-pharmaceutical, medical device, and Ayurvedic sectors. Their key services include Clinical Operations, Data Management, Biostatistics, Medical Writing, and Regulatory Affairs. Role Description This is a full-time on-site role for a Quality Assurance Executive located in Gurgaon. The Quality Assurance Executive will be responsible for implementing and maintaining quality standards, conducting quality audits, and managing quality control processes on a day-to-day basis. Qualifications Quality Control and Quality Assurance skills in Clinical Trial Quality Management and Quality Auditing skills in Clinical Trial Strong attention to detail and analytical skills Knowledge of regulatory requirements and compliance in Clinical Trial Excellent communication and teamwork skills Bachelor's degree in Life Sciences, Chemistry, Biology, or related field Show more Show less
Company Description AlzaSyno Life Sciences is a CRO (Contract Research Organization) offering services in clinical operations, data management, biostatistics, medical writing, and regulatory affairs tailored to pharmaceutical, bio-pharmaceutical, medical device, and Ayurvedic sectors. Our services include study design and management, data collection and validation, statistical analysis, documentation preparation, regulatory submissions, and more. Role Description This is a full-time on-site role for a Business Development Manager located in Gurugram. The Business Development Manager will be responsible for identifying business opportunities, building and maintaining client relationships, developing strategic partnerships, and promoting the company's services to key stakeholders. Qualifications Business Development, Sales, and Client Relationship Management skills Excellent communication and negotiation skills Strategic thinking and problem-solving abilities Experience in the CRO industry or life sciences sector Bachelor's degree in Business, Life Sciences, or related field Knowledge of regulatory processes and industry standards Ability to travel as needed for client meetings and conferences Show more Show less
Job Description: Biostatistician Company: AlzaSyno Life Sciences Location: Gurugram, Haryana Work Schedule: 5 Days a week (Monday - Friday), 9:00 AM to 6:00 PM Experience: 5+ Years About AlzaSyno Life Sciences: AlzaSyno Life Sciences is a leading Contract Research Organization (CRO) dedicated to providing high-quality, full-service clinical research solutions to the global pharmaceutical, biotechnology, and medical device industries. We are committed to scientific excellence and accelerating the development of life-changing therapies. Position Summary: We are seeking a highly motivated and experienced Biostatistician to join our dynamic Biostatistics and Programming team. The ideal candidate will play a critical role in the design, analysis, and reporting of clinical trials, ensuring the highest standards of statistical integrity and regulatory compliance. You will collaborate closely with cross-functional teams to deliver robust statistical outputs that drive key development decisions. Key Responsibilities: 1. Statistical Analysis Plan (SAP) & Protocol Development: Provide expert statistical input into the design of clinical trials, including sample size calculation, randomization, and endpoint selection. Author, review, and finalize detailed Statistical Analysis Plans (SAPs) for assigned studies. Develop and review statistical sections of clinical study protocols. 2. Data Standards & Programming: Utilize advanced statistical programming skills in SAS (primary), R , STATA , and SPSS to analyze clinical trial data. Develop and validate SAS programs for the generation of safety and efficacy analysis outputs, including Tables, Listings, and Figures (TLFs) . Ensure adherence to CDISC standards , including SDTM and ADaM models, for all datasets and deliverables. Perform quality control (QC) review of datasets and TLFs produced by other team members. 3. Clinical Study Reporting: Lead the statistical analysis and interpretation of clinical trial results. Author and review the statistical sections of Clinical Study Reports (CSRs), integrated summaries, and publications. Ensure all statistical deliverables are accurate, complete, and produced within agreed timelines. 4. Quality & Compliance: Ensure all statistical activities comply with GCP , ICH guidelines, relevant regulatory requirements (FDA, EMA, etc.), and company SOPs. Serve as a key point of contact for internal and external audits and regulatory inspections related to biostatistics. Implement and maintain best practices for programming and data validation. 5. Collaboration & Communication: Collaborate effectively with Clinical Data Management, Medical Writing, Pharmacovigilance, and Project Management teams. Communicate complex statistical concepts and results clearly and effectively to non-statistical colleagues and clients. Qualifications & Skills: Education: Master's degree (M.Sc.) in Statistics or Biostatistics from a recognized university. Experience: Minimum of 5 years of experience as a Biostatistician within a Pharma, Biotech, or CRO environment. Technical Skills: Essential: High proficiency in SAS (Base, Stat, Graph, Macro). Highly Desirable: Strong working knowledge of R , STATA , and SPSS . In-depth knowledge of CDISC standards ( SDTM , ADaM ). Therapeutic Knowledge: Experience across various therapeutic areas is preferred. Regulatory Knowledge: Thorough understanding of GCP , ICH guidelines, and regulatory submission requirements. Soft Skills: Excellent problem-solving and analytical skills. Strong attention to detail and commitment to data quality. Ability to work independently and manage multiple priorities in a fast-paced environment. Effective communication and interpersonal skills. What We Offer: A competitive compensation and benefits package. Opportunities for professional growth and career development. A collaborative and supportive work environment. Exposure to a wide range of global clinical projects.
Company Description AlzaSyno Life Sciences provides a wide range of Contract Research Organization (CRO) services tailored to pharmaceutical, bio-pharmaceutical, medical device, and Ayurvedic sectors. The company specializes in clinical operations, including study design, management, and compliance, as well as data management services, such as collection, validation, and database maintenance. AlzaSyno Life Sciences also offers biostatistics expertise through statistical analysis and reporting to support regulatory submissions. Additionally, their services include medical writing and the preparation of all required documentation for clinical trials and regulatory approvals. With a focus on regulatory strategy and acting as a liaison with regulatory agencies, the company ensures efficient processes and full compliance with local and international standards. Role Description This is a full-time, on-site role for an Information Technology Administrator, based in Gurugram. The IT Administrator will be responsible for ensuring the smooth operation of IT systems and networks, providing technical support to the organization, and conducting system and network administration tasks. Key responsibilities include troubleshooting IT issues, managing and maintaining IT infrastructure, and implementing necessary updates and upgrades to ensure optimal system performance and security. Qualifications Proficiency in Technical Support to provide prompt and effective solutions to IT-related issues. Expertise in Network Administration, including configuration, monitoring, and troubleshooting of network systems. Experience with System Administration, including installation, configuration, and maintenance of hardware and software systems. Strong Troubleshooting skills to diagnose and resolve technical problems efficiently. Comprehensive understanding of Information Technology concepts, tools, and best practices. Excellent analytical and problem-solving skills to handle complex IT challenges. Ability to work collaboratively with cross-functional teams to meet organizational IT needs. Bachelor's degree in Information Technology, Computer Science, or a related field preferred. Relevant certifications such as CompTIA Network+, CCNA, or Microsoft Certified: Azure Administrator Associate are advantageous.