175 Drug Development Jobs - Page 3

Assist in dispensing prescription and over-the-counter medications accurately. Provide medication counseling to patients under supervision. Maintain patient records and ensure documentation is accurate and up to date. Ensure inventory is managed effectively restock shelves, check expiry dates, and maintain proper storage. Stay informed about new drugs and pharmacy regulations. Collaborate with healthcare professionals to ensure optimal patient care. Adhere to ethical and regulatory guidelines related to pharmacy practice. Familiarity with pharmacy management systems/software. Basic understanding of medical terminology.

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

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

Position Summary: The R&D Data Modeler develops conceptual and logical data models for initiatives, programs, and cross-R&D capabilities. This role is critical for creation of data models and ontologies, and upkeep of models even beyond the conclusion of a project. Data modelers will apply and assist in the definition and governance of data modelling and design standards, tools, best practices, and related development of any R&D data capability. Main responsibilities: Engage in data management and analytics projects; understand, advise, and execute on data flow optimization (e.g., data capture, integration and use across R&D) Understand the data-related needs for various cross-R&D capabiliti...

About the job Join our Hyderabad Hub, build a career and you can be part of transforming our business while helping to change millions of lives. Ready? Within the Clinical Trial Team (CTT), the Senior Study data manager is responsible for leading the end-to-end Clinical Data Management (CDM) activities and study deliverables supporting study set-up, conduct and close-out, complying with GCP and applicable regulatory guidance. He/She is accountable for the quality of CDM deliverables and for ensuring accurate and reliable study data, therefore guaranteeing the reliability of the study results. He/She ensures activities are completed according to agreed standards and timelines. He/She provides...

Contracting deliverables Exercise good judgment in balancing the risks to the client in making budget and contractual decisions against the impacts to client clinical trial timelines. Follow client processes to develop, negotiate, track and execute global clinical study agreements with institutions and investigators participating in sponsored clinical trials. Work with partners to develop and oversee the global site budget process. Work with clinical trial sites and directly negotiate cost, business and contractual terms and conditions with investigators/institutions, making changes to contract templates within the Legal division approved parameters. Lead study level site contracting activit...

- Sound knowledge and experience in working with statistical compute and data science platforms - Proven experience in Architectural Designing, implementing and governing large programs. - Solid understanding of clinical trial processes and leveraging quantitative sciences and toolsets in regulatory and exploratory pathways -Ability to assess landscape with knowledge of industry trends in clinical data flow, CDISC standards, open-source technologies, evolving analysis toolsets and cloud compute to drive sustainable roadmap of technology in Clinical enablement for Study design through data submission. About the Role Key Responsibilities: Oversee architectural activities for a specific busines...

As an Associate Scientist at Novartis, you will be responsible for designing, planning, performing, interpreting, and reporting scientific experiments for the development and timely delivery of drug products within a project team. You will also manage technical lab and plant activities. In this role, you will work closely with a multifunctional project team led by a Project Leader to prepare and deliver drug substances, drug products, and processes. Your key responsibilities will include: - Meet quality, quantity, and timeline goals in all projects while aligning with the overall drug development process. - Plan, organize, perform, and document scientific experiments in collaboration with pr...

As a Global PV Sr. Scientist at Amgen, you will play a crucial role in collaborating with the Therapeutic Safety Teams on safety assessment activities related to medical and scientific operations. Your expertise will be essential in providing scientific and compliance support to Global Patient Safety (GPS) as required. Your key responsibilities will include: - Directing the planning, preparation, writing, and review of portions of aggregate reports - Coordinating liaison activities with affiliates and other internal partners at Amgen regarding products - Providing oversight to staff on safety in clinical trials, reviewing study protocols, statistical analysis plans, clinical study-related do...

As a Site Contracting Team Lead (SCTL) at Pfizer, you will be responsible for planning and achieving contract execution targets, managing risks to APAC targets, and collaborating with other functional lines and planners to effectively plan, prioritize, and allocate resources for studies within your remit. You will provide expertise and support to your team and other site contracting professionals, helping them independently resolve issues related to site contracting and cross-functional dependencies. Additionally, you will partner with other countries to optimize portfolio support, manage country and study level issues within your scope, and support regional site contracting needs through pr...

Brief Job Description - Consultants coordinate desk-based research (incl. clinical, scientific, regulatory, commercial, etc.) on high-importance topics and generate reports which incorporate critical and analytical thinking. They are expected to keep abreast of developments in their assigned therapeutic area/s and continuously assess the impact of any new events/findings. They should have experience in handling clients, mentoring, attending/covering healthcare conferences and project planning. Candidate - Highly enthusiastic and committed individuals with deep knowledge of the biopharmaceutical space and strong analytical skills are sought for this position Candidates are expected to be meti...

You will be a key participant in the development of the GSC innovation & business transformation strategy at Lilly. Your role involves leading the implementation of the strategy at the local site by collaborating with global and regional functional and cross-functional partners. You will develop and maintain core and emerging capabilities to set GSC up for Best-in-Class content creation, strategy, and delivery. This includes capabilities such as regulatory and submission writing, transparency, publication writing, strategy, and planning, structured and component authoring, and data visualization. Your responsibilities will also include partnering with a team of functional experts to execute ...

Role Overview: As a Senior Clinical Research professional at Ascentrik Research Pvt. Ltd, you will be responsible for leading and managing a research team to curate accurate, timely, insightful, and comprehensive data and intelligence for Beacon Targeted Therapies. You will work closely with UK-based clients, analyze relevant information, and ensure project deliverables are met. Additionally, you will be part of a global network of life science researchers, focusing on dynamic products in cutting-edge life science areas. Key Responsibilities: - Lead and manage a research team to curate accurate, timely, insightful, and comprehensive data and intelligence - Identify and analyze the most relev...

The Technology Platform Director / Technology Product Director is responsible for managing the Life Cycle of one or more GCO business technology products, including strategic roadmap definition, development, configuration, release, and ongoing performance. Success in this role hinges on aligning technology product features and functionality with business domain requirements and user needs. This position requires a forward-thinking approach, the ability to anticipate future user needs, and a commitment to simplifying the technology landscape for improved experiences. Working closely with IT stakeholders, the Technology Platform Director continuously enhances the functionality and performance ...

Honour CDMO Business : Honour is a leading Contract Development and Manufacturing Organization (CDMO) headquartered in India, serving global pharmaceutical and biotech companies. With integrated capabilities across process development, analytical services, scale-up, and commercial GMP manufacturing, Honour supports its partners throughout the drug development lifecycle. Our mission is to deliver reliable, high-quality, and cost-effective solutions, enabling customers to accelerate molecules from discovery to commercialization. Responsibilities : Identify, evaluate, and develop new business opportunities across the US WestCoast region . Establish, strengthen, and expand client relationships t...

In close collaboration with the Global Program Safety Lead (GPSL), you will provide robust safety evaluation expertise and medical innovation to enhance patients" lives and influence Novartis" overall results. As a part of the Medical Safety organization, your priority will be ensuring the safety of patients, optimizing patient safety for assigned compounds, and sharing responsibility for integrating, analyzing, and evaluating internal and external safety information throughout the product lifecycle management. Your main responsibilities will include monitoring the clinical safety of projects/products, conducting medical assessments for cases, identifying safety signals, preparing safety dat...

Premier Research is seeking an Associate Database Developer for an 8-month contract in India to join the Functional Services Provider (FSP) team. In this role, you will contribute to the transformation of life-changing ideas from biotech, medtech, and specialty pharma companies into new medicines, devices, and diagnostics. Your work will play a crucial role in saving and enhancing lives, and we value our team members as our most important asset for achieving success. We are committed to supporting your growth, providing you with the necessary skills and opportunities to thrive at work while maintaining the flexibility and balance that your life demands. Your input shapes our work culture, an...

About You Education (BPharm/MPharm/MSc in Biotechnology, Microbiology, Lifesciences) Minimum 2 years of experience inanalyzing and updating clinical reports In-depth knowledge of clinical trials, pharmaceutical drug pipelines, drug development, and clinical phases Excellent English written and verbal communication skills. It would be great if you also had . . . Experience in secondary research related to clinical information Ability to delve deep into content and results. What will you be doing in this role? Actively seek out information about Clinical trials, analyze, cross reference, and update all new or previously updated information in the Clinical trials records from various sources, w...

We are looking for an Associate STEM Content Analyst to join our Biological Drugs team in Chennai (India). This is an amazing opportunity to work on content analysis for our Cortellis Drug Discovery Intelligence (CDDI) product. The team consists of 9 members based across Chennai, Hyderabad and Barcelona (Spain) and this role reports to the Biologicals Team Manager. We have a great skill set in Biology, Immunology, Pharmacology, Pharmacokinetics andcomplementary skill sets to address challenges in drug discovery, including new biological drugs identification and drug repositioning. We would love to speak with you if you have an understanding of biological drug products. About You experience, ...

The Associate Medical Expert in Translational Clinical Oncology (TCO) serves as the medical leader for global, roll-over, and long-term follow-up studies, as well as studies in the close-out phase. Additionally, they provide medical support for assigned components of active TCO studies under the guidance of a Clinical Program Leader (CPL) or Medical Expert. TCO, a department within the Biomedical Research division, specializes in designing and conducting early-phase clinical studies in cancer patients, bridging the gap between drug discovery and late-phase clinical development to deliver innovative oncology treatments. In this role, your major responsibilities include providing medical suppo...

The Regulatory Compliance Team Lead will be responsible for overseeing a team of regulatory CMC professionals performing assessment of operational changes for regulatory reportability for Amgen products across phases of development, modality, and countries. This role is accountable for hiring, training and retaining talented regulatory CMC regulatory staff, in alignment with the operational objectives of the wider RA CMC department. They are accountable for continuous improvement, through the development and refinement of processes, and partnership with colleagues in other functions to develop systems and tools that improve the speed and efficiency of operations over time. They exemplify the...

Major accountabilities: Provides medical support to Clinical Program Leader (CPL) leading the program. Medical support may include, but is not limited to, contributing to clinical sections of protocols and/or amendments, Informed Consents, publications, regulatory documents such as Investigator Brochures, responses to Health Authority questions and conducting ongoing review of clinical trial data, with oversight of TCO deliverables. May act as the medical monitor to support overall program safety reporting (e.g., Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety Team. May represents CPL at project team meetings (e.g. CTT) and may pro...

Recruits and manages a team Develops objectives for Medical Safety in collaboration with other Medical Safety Team leads and MSO head in alignment with Patient Safety and Sandoz Goals and Objectives. Development and retention of talents. Leads the performance management process for their team Leads the day-to-day safety activities of the assigned team as per allocated portfolio. Oversees the assignment of activities within the team and ensures the timely delivery and appropriate quality oversight of Sandoz safety deliverables, including but not limited to Medical Risk Assessments, PSURs and RMPs Enhances operational, scientific and clinical experience of Safety Leads/Experts through continuo...

Major Accountabilities Domain Expertise: Apply in-depth knowledge of life sciences, including drug discovery, development, and clinical trials, to support AI-driven initiatives. Stay abreast of the latest advancements in Generative AI and their potential applications in the life sciences industry. Business Analysis: Collaborate with stakeholders to gather, document, and analyze business requirements, ensuring alignment with organizational objectives. Liaise with stakeholders to gather and understand the business needs related to Generative AI solutions Conduct thorough analyses of business processes and workflows, identifying opportunities for AI-driven improvements and efficiencies. Develop...

Your Key Responsibilities: Your responsibilities include, but not limited to: Technical Support to internal Manufacturing Sites and CMO s: As a Technical Expert to the assigned manufacturing site internally or CMO, ensure and improve product process capability, to keep the knowledge of process up to date and to maintain the product in constant state of validation. Implement Science- and Risk-based approaches to ensure that product quality can be sustainably reproduced. Ensure the availability of all relevant Technical Documentation such as protocols, reports, Risk Assessments, Concept papers, Scientific Justifications based on significant body of information generated regarding the product &...