186 Pharmacokinetics Jobs - Page 5

About The Job We are seeking a skilled Data Platform Engineer with expertise in High-Performance Computing (HPC) and cloud computing to support our scientific research activities globally (Canada, US, France and Germany mostly). The ideal candidate will have experience in managing and optimizing Linux-based HPC environments, as well as proficiency in AWS cloud services. This role involves collaborating with various R&D groups to provide technical support and drive continuous improvements in our computing infrastructure. The candidate should be adept at handling both open-source and commercial software across different R&D fields. What You Will Be Doing Support in-silico activities in the Bos...

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolve...

Roles in DMPK we are hiring for : Bioanalytical / Peptides, Antibody drug conjugates and ASOs In vitro ADME / cell biology, cell permeability hepatocytes, 3D cultures, image analysis, drug transporters and enzymology PK/PD, Modeling and Simulations / Pheonix WinNonlin, R, Monolix, NONMEM, MATLAB, or any other custom-built software In vitro Toxicology/ 3D cultures-Organoids and Spheroids Key Responsibilities : Knowledge of data compilation and interpretation for test compound classification systems, either as substrates or uptake inhibitors. Ability to understand and read data, identify data variability, and participate in data review cycles with the QA team. Commitment to delivering data wit...

Department: DMPK (Drug Metabolism and Pharmacokinetics) Location: Hyderabad About Sai: Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, and inclusivity. We embrace diversity and ...

As an In vitro Bioanalytical Scientist at Syngene, based in Hyderabad, you will be responsible for participating in sample processing for PK and ADME assays, as well as handling LCMS/MS. Your role will involve adapting to a dynamic team environment, processing various matrices samples for PK studies, optimizing test compounds manually and automated on LCMS/MS, and independently handling HPLC for UV-based sample analysis. Additionally, you will be expected to develop methods with the team lead, document lab notebooks online, and manage compounds effectively. You will need to demonstrate expertise in column selection, mobile phase selection, solvent preparations, and sample processing techniqu...

Job Title: Associate Professor / Professor - Pharmacology / Pharmaceutics Location: K.R. Mangalam University, Haryana Department : School of Medical and Allied Sciences (Pharmacy) Employment Type: Full-time Job Summary: K.R. Mangalam University is looking for a highly qualified Professor in Pharmacology /Pharmaceutics to lead academic and research activities in the School of Medical and Allied Sciences. The candidate will be responsible for teaching, research, curriculum development, and industry collaboration while mentoring students and faculty members. Key Responsibilities: Teaching & Academics: Deliver lectures, tutorials, and practical sessions in Pharmacology /Pharmaceutics and related...

You will be responsible for providing drug metabolism and pharmacokinetic support for discovery programs. Your main duties will include monitoring Pharmacokinetics studies, supporting bioanalysis, and offering pre-clinical ADME lead optimization support to small molecule Drug Discovery programs across various therapeutic areas. You will be working as a DMPK subject matter lead in multidisciplinary/cross-functional teams to understand the Chemical Structure ADME relationships and design appropriate strategies to enhance the Drug like Properties of the New Chemical Entities. To be successful in this role, you should have 2-5 years of experience in GLP with either an M.Sc. or Ph.D. degree. You ...

Job Summary – Clinical Research (Micro Labs) Overview: Responsible for independently planning, executing, and managing clinical trials—mainly bioequivalence, but also safety and efficacy studies—ensuring they are completed on time, within budget, and in compliance with regulatory and company standards. Key Responsibilities: Contribute to formulation development. Define clinical strategy (Study designs, Sample size, healthy volunteers or patient studies). Lead and manage BABE studies from planning through execution, data analysis, and reporting. Collaborate closely with team leaders and oversee operational activities. Select and manage CROs, ensuring cost-efficiency, regulatory compliance, an...

As a Senior R Developer at MResult, you will play a crucial role in supporting the development, validation, and deployment of models and tools used in drug development and clinical research. Your responsibilities will include developing and maintaining R scripts, packages, and Shiny applications for data analysis and visualization. You will be involved in performing statistical analysis and data manipulation related to clinical trials and PK/PD data. Collaboration with pharmacometricians and clinical scientists will be key as you work together to develop PK models and support modeling workflows. Automating data cleaning, processing, and reporting tasks will be part of your daily activities. ...

Date: 23 Jul 2025 Location: Kolthur Shamirpet, Medchal, TG, IN, 500078 Custom Field 1: Discovery Services Job Title: Invitro Bioanalytical Scientist Job Location: Hyderabad About Syngene : Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per...

Job Description: Toxicologist / Preclinical Scientist We are seeking a skilled Toxicologist / Preclinical Scientist to join our team. The ideal candidate will be accountable for conducting toxicological risk assessments and overseeing preclinical experimental research. 1. Key Responsibilities: Toxicological Risk Assessments • Derive Health-based Exposure Limits & support occupational hazard assessment (PDE/OEL) for pharmaceutical molecules in adherence to regulatory standards. • Conduct Toxicological Risk Assessments (TRA) for pharmaceuticals, excipients, intermediates, chemicals, cleaning agents, residual solvents, elemental impurities, and degradation products. • Perform Genotoxicity Hazar...

The candidate will undergo a self-financed job-oriented patent analyst training at the Indian Institute of Patent and Trademark. On successful completion of the training, they will be placed for full-time patent analysis in the pharmaceutical domain. Required Candidate profile Scientific and Analytical Thinking Eager to work in drugs and formulation Candidates must have sound knowledge about the subjects they study in Graduation

Role & responsibilities Experience Minimum 3-5 years of experience in handling ADME assays and HPLC and LCMS/MS Skills and Capabilities Expertise in column selection, mobile phase selection, solvent preparations and sample processing techniques such as protein precipitation, liquid-liquid extraction and solid phase extraction is mandatory Sample processing of New chemical entities from various in-vitro and in-vivo studies executed in Preclinical discovery by using appropriate extraction methods Should be able to develop and validate LC-MS based qualitative/quantitative methods and apply them in routine analysis Should be well versed with internet-based literature search and capable of implem...

As a Senior Scientist in Clinical PBPK Modeling at AstraZeneca, located in Bengaluru, Karnataka, India, you will play a crucial role in advancing clinical drug development through the application of innovative and quantitative approaches. Your primary responsibility will involve utilizing physiologically-based pharmacokinetic (PBPK) and translational modeling tools to facilitate clinical PK projections for drug-drug interactions (DDIs), pediatric and specific populations, and other critical clinical development inquiries. Collaboration with Drug Metabolism and Pharmacokinetic (DMPK) Scientists, as well as Clinical Pharmacology scientists, will be key in generating mechanistic models. Your ex...

We are looking for an experienced and dedicated Clinical Pharmacist to join our team The candidate should have a minimum of 1 year of experience Review and evaluate medication orders to ensure appropriateness, safety, and efficacy based on patient-specific factors such as age, condition, and comorbidities Collaborate with physicians, nurses, and other healthcare professionals to develop and implement patient-specific medication therapy plans Monitor patient progress and outcomes to adjust medications as needed Educate patients and caregivers on the proper use, side effects, and interactions of prescribed medications Ensure compliance with established protocols, regulatory requirements, and h...

Institution: Divy Jyoti Pharmacy College, Sidhi Qualification: M.Pharm in Pharmacology Experience: 0–5 Years Job Type: Full-Time | Permanent Responsibilities: Teach topics like drug action, toxicology, and therapeutics to D.Pharm and B.Pharm students. Conduct lab work, including simulations or basic animal model theory (as per norms). Mentor students on pharmacological case studies and clinical relevance. Participate in departmental meetings, exam duties, and academic planning. Preferred Skills: Deep understanding of pharmacokinetics and pharmacodynamics Clear communication Additional familiarity with biology and patient counselling preferred Job Type: Full-time Pay: ₹20,000.00 - ₹80,000.00 ...

You are looking for a Study Director - Toxicology position at Syngene in Bangalore. As a Study Director, you will be responsible for overseeing GLP toxicology studies in compliance with global regulatory guidelines. Your role will involve coordinating with cross-functional teams, conducting in-life phases of toxicology studies in various animals, administering doses, collecting blood samples, and ensuring adherence to safety protocols and SOPs. Key Responsibilities: - Serve as a Study Director for in vivo toxicology studies, ensuring scientific, technical, and regulatory compliance - Coordinate with local cross-functional teams for the execution of toxicology studies - Conduct in-life phases...

As an ideal candidate for this position, you should hold a Master's degree in Pharmacy with a specialization in Pharmacology or Pharmaceutical Analysis coupled with 5-8 years of experience. Alternatively, a Ph.D. with 2-5 years of relevant experience in PK/PD Modelling and PBPK models would also be considered. Your responsibilities in this role would include developing and applying pharmacometric models to aid in drug development and regulatory submissions. You must possess a deep understanding of non-linear mixed effects modelling and be proficient in using software tools such as PBPK models, Phoenix, R, PoPK, QSP modelling, or similar platforms. Your expertise in pharmacokinetics/pharmacod...

Date: 26 Jun 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Discovery Services Job Description Job title: Study Director - Toxicology Department : Safety Assessment Job location: Bangalore About syngene: syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expect...

Summary Join our dynamic and innovative global Computer-Aided Drug Discovery (CADD) group, now expanding to India! Be a part of our Hyderabad team, where we unite diverse talents to revolutionize the validation and development of new targets in Biomedical Research. As a driving force behind drug discovery, we are excited to find an exceptional computational scientist like you to join our global ranks. Imagine the opportunity to unlock hidden knowledge and disruptive insights from the vast and invaluable data collected by one of the world's most renowned pharmaceutical companies. We need your expertise, experience, and unwavering passion to help us extract this wealth of information. Collabor...

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company dedicated to developing innovative products that cater to the needs of underserved patients. With a focus on providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to expand its broad commercial product portfolio and robust late-stage pipeline. The company's patient-centric products cover various therapeutic areas such as cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, benefiting millions of patients worldwide. For more information about Azurity, please visit www.azurity.com. Azurity Pharmaceu...

Core Responsibilities: 1. Design and Analyze PK Studies o Plan clinical PK studies synopsis and feasibility o Analyze PK data using modeling and simulation tools (e.g., Phoenix WinNonlin, R software). o Interpret PK parameters such as C_max, AUC, T_max, half-life, clearance, and volume of distribution. 2. Support Drug Development o Provide PK and statistical input in clinical development phase studies protocol o Evaluate food effect, drug-drug interactions (DDIs), and bioavailability/bioequivalence studies and provide scientific inputs for study design & protocol preparation o Support dose selection and optimization strategies for pivotal study design. 3. Regulatory Submissions o Deep unders...

Company Description Aizant® is an integrated drug development solutions provider, established by experienced pharmaceutical professionals with global exposure. As a rapidly growing contract research organization (CRO), Aizant partners with health care companies globally to support new molecular entities (NMEs), generics (ANDAs), and over-the-counter (OTC) products. We offer comprehensive solutions across drug development stages including preformulation, formulation development, analytical development, cGMP scale-up, stability, bioavailability, bioequivalence, bioanalysis, pharmacokinetics, and clinical diagnostics. Our mission is to add exponential value to our clients’ R&D programs from mol...

Preferred candidate profile M. Pharm (Pharmacology) / M.Sc. (Biochemistry / Pharmaceutical Chemistry) with 6-9 years or Ph.D. with 2-5 years' experience in PBPK & PK/PD modelling & Gastro plus; Simcyp software Role & responsibilities Experience in the development and application of pharmacometric models to support drug development and regulatory submissions Extensive experience with non-linear mixed effects modelling Proficient with software tools like PBPK models, Phoenix, R, PoPK, QSP modelling or similar platforms Strong background in pharmacokinetics/pharmacodynamics (PK/PD) modelling, First-in-human dose predictions. Collaborate with clinical pharmacology, biostatistics, and other inter...

Preferred candidate profile M. Pharm (Pharmacology / Pharmaceutical Analysis) / M.Sc. (Biochemistry / Pharmaceutical Chemistry / Analytical Chemistry) with 3 - 6 years experience in Bioanalytical DMPK & Invivo PK. Role & responsibilities Planning and execution of invivo preclinical pharmacokinetic studies, invivo tissue distribution & mass balance studies in rodents. Expert in method development of NCEs using LC-MS/MS system Well verse with extraction techniques of molecules from various matrices like plasma/urine/tissues Experienced in surgical skills for rodents PK, excretion studies Conduct Bioanalysis of samples from in-vivo pharmacokinetic, tissue distribution studies, PK-PD & TK studie...