5 Experimental Designs Jobs

As an Invivo Pharmacology Scientist at Syngene, located in Bangalore, you will play a crucial role in conducting research projects related to animal models of Neuropathic pain. Your responsibilities will include setting up experimental designs, analyzing data, recording observations, and communicating research results to supervisors and clients. You must possess excellent technical knowledge and experience in this field, along with the ability to lead cross-functional teams to ensure timely and high-quality project delivery. Your role will require hands-on experience in executing neuropathic pain and arthritis models in rats and mice, as well as proficiency in surgical techniques such as SNL, CCI, PSNL, and SNI. Additionally, you will be responsible for handling instruments like Hargreaves apparatus, Dynamic plantar aesthesiometer, and Von Frey filaments, among others, for recording pain readouts. To excel in this role, you should have a Master's degree in Pharmacology or M.V.Sc Pharmacology, with 1-9 years of experience in the field. Strong organizational skills, attention to detail, and the ability to work independently are essential. You must also demonstrate leadership capabilities by effectively collaborating with internal and external stakeholders, adhering to safety protocols, and maintaining a culture of excellence, integrity, and professionalism. By championing effective Environment, Occupational Health, Safety, and Sustainability (EHSS) practices, you will contribute to the overall success of Syngene. Your commitment to upholding the company's core values and fostering a culture of safety and sustainability will be key to your leadership role within the organization. If you are a dedicated professional with a passion for pharmacology and a desire to make a difference in the field of in-vivo Pharmacology, we encourage you to apply for this role. Join us at Syngene and be part of a team that values excellence, integrity, and professionalism in all aspects of our work.,

You are a candidate who holds a Master's degree in Chemistry, Polymer, Material Science, or Chemical Engineering with 2 to 4 years of experience. Your experience should include working with polymer processing technologies and equipment, preferably in manufacturing environments involving thermoset polymers and polymer processes. It is preferred that you have engineering experience in investigations, defining test protocols, and analyzing statistical data. Additionally, experience with executing experimental designs (DOE) in a manufacturing setting would be advantageous, as well as transitioning new processes and products to manufacturing. As a candidate, you should possess personal attributes such as networking, teamwork, open-mindedness, listening skills, and effective communication. Management skills including customer focus and result orientation are essential. Transparent, authentic, and inclusive leadership qualities are highly valued in this role. Moreover, your ability to work in a plant environment is crucial for success in this position.,

As a Biostatistician at CPVIA, a clinical data analytics solutions company in Hyderabad, you will utilize your expertise in statistical programming and consulting to support pharmaceutical, biotechnology, and medical device companies. Your primary focus will be on accelerating drug development activities while maintaining high quality standards and cost efficiency through collaboration with a team of experienced professionals. With a minimum of 3 years of experience in the pharmaceutical industry, you will play a crucial role in providing internal statistical support by closely working with lab scientists, technicians, statisticians, and programmers. Your responsibilities will involve collaborating with various stakeholders to facilitate drug development activities and ensure successful project outcomes. To excel in this role, you are required to hold a university degree in Sciences or Engineering, with a post-graduate qualification in Biostatistics or equivalent statistical experience. You should have a strong grasp of statistical theory, diverse methodologies, and experimental designs. Proficiency in SAS, R (and JMP) is essential, along with effective communication skills to bridge theoretical concepts with practical applications. Being a team player is vital as you will be expected to share knowledge within multidisciplinary teams and contribute to study oversight and delivery. Experience in developing protocols, Statistical Analysis Plans (SAP), Tables, Figures, and Listings (TFL) is advantageous. Additionally, your technical skills in power calculation, simulations, and Quality Data Model (QDM) will be valuable assets in this role. If you meet the qualifications mentioned above and are passionate about making a meaningful impact in drug development, we encourage you to apply by submitting your resume to info@cpvia.com. Join us at CPVIA and be part of a dynamic team dedicated to driving innovation and excellence in clinical data analytics.,

As a Biostatistician at CPVIA, a clinical data analytics solutions company based in Hyderabad, you will play a crucial role in providing statistical programming outsource and statistical consulting services to pharmaceutical, biotechnology, and medical device companies. Your primary responsibility will be to offer internal statistical support by collaborating closely with lab scientists, technicians, and other statisticians/programmers within the team. Your expertise will be instrumental in supporting various drug development activities for our clients. To excel in this role, you must have a minimum of 3-10 years of experience in the pharmaceutical industry. A background in Sciences or Engineering at the university level, complemented with a post-graduate degree in Biostatistics or equivalent statistical experience, is essential. Proficiency in SAS, R (and JMP), and a deep understanding of statistical theory across various methodologies and experimental designs are prerequisites for this position. We are looking for a team player who can effectively communicate and collaborate within multidisciplinary teams. Your role will involve contributing to the development of protocols, SAPs, and TFLs, as well as overseeing studies and ensuring timely delivery. Strong technical skills in power calculation, simulations, and QDM will be beneficial in fulfilling the requirements of this role. If you meet the qualifications mentioned above and are passionate about contributing to the acceleration of drug development activities with top-notch quality and cost-effectiveness, we invite you to share your resume with us at info@cpvia.com. Join our experienced and expert team at CPVIA to make a significant impact on the pharmaceutical and biotechnology sectors.,

Position: Product Development Specialist Location Bangalore (KA) / Vapi (GJ) Duties And Responsibilities Conduct field evaluations of new products, utilizing statistical design for trial results to support informed decision-making for projects. Analyse trial results comprehensively and recommend actionable insights. Identify market gaps and farmer pain points to generate innovative product ideation Developing trial protocols and experimental setups for different types of trials, such as, screening, evaluation of product concepts and dose optimization trials Create organizational excitement about new product pipelines by conducting: proof-of-concept trials, reason-to-believe trials, product technical knowledge trials Position products by highlighting their unique value propositions. Prepare detailed trial summaries and biological dossiers. Transfer comprehensive biological dossiers to the regulatory team for compliance. Develop trial protocols aligning with patent requirements, including Colby formulation suitability. Conduct data analysis and summaries in patent-compliant formats to enhance the success rate of patent grants. Skills & Competencies Strong analytical skills with proficiency in statistical tools and experimental designs. Expertise in trial protocol creation and evaluation techniques. Knowledge of patent processes and data requirements in the CP industry. Excellent communication and documentation skills to create reports, summaries, and technical dossiers. Ability to bridge the gap between field insights and market needs to drive product innovation. Other Requirements Flexibility to travel between Bangalore and Vapi (GJ) as needed. This role is instrumental in shaping the future of our product pipeline and ensuring the delivery of value-driven solutions for farmers and stakeholders,