1075 Pharmacology Jobs - Page 6

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. Job Summary Roles and Responsibilities Handling entire Secretarial compliances of Charles River under the Companies Act and to ensure that Company’s interests are protected at all times Handling entire Secretarial compliances of Charles River under the Companies Act 2013 and Secretarial Standards including but not limited to; Ensuring the company complies with all legal and statutory requirements, including internal policies, external regulations, and corporate governance requirements. Handling other statutory compliances required under the Shop & establishment Act, labour laws and other State & Central Government Acts applicable to Charles River Laboratories Pvt Ltd. from time to time. Maintenance and safe keeping of Register of members/ Share holders, Directors, Minute books of General and Directors meeting. Submission of returns to Registrar of Companies. Under directive of board, to issue notices for Board & General meeting, Coordinating board / general Meeting and follow up activities thereon. . To conduct Correspondence with members w.r.t Share capital matters and Share Transfer Matters. Assisting legal department in preparing legal documents and Maintenance of Agreement Copies. Review of general contracts including engagement letters, lease agreements, no objection certificates, non-disclosure agreements. Sending out alerts on the respective due dates Compliance with the clauses mentioned in the agreement. Required to carry out related duties and responsibilities and any other assignments entrusted to from time to time Updating of various Statutory Registers. Filing of various Forms with RBI. Providing legal guidance /advice to the management Liaising with external agencies and advocates on legal aspects Drafting and reviewing Policies and terms of reference of committees on an annual basis implementing processes or systems to help and ensure good management and compliance with Law Job Qualifications Desired Candidate Profile: Education PG : CS Experience: 2 to 5 years Salary: INR 7 to 9 lakhs per annum. Must be presentable, knowledgeable and good in secretarial compliances. Qualified CS with ability to join as full time CS Role. Must possess excellent communication skills Must possess a positive attitude and a team player. About Discovery Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 350 patents and 80 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction. 228758

You are a Senior Manager of Medical Coding Operations specializing in Same Day Surgery, based in Airoli, Navi Mumbai. With over 11 years of experience in the medical coding field, you possess in-depth knowledge of Surgery Medical Coding guidelines, ICD-10, and CPT coding techniques. Your strong foundation in Anatomy & Physiology, Advanced Medical Terminology, Pharmacology, and Psychology, along with proficiency in MS Office, excellent communication, and interpersonal skills, make you an ideal candidate for this role. Your primary responsibilities include managing coding transitions, providing training and leadership to the coding team, understanding and exceeding client expectations, leading project transitions, making effective decisions, conducting research and analytics, mentoring coders, collaborating with stakeholders, overseeing client interactions, and managing a team of multispecialty coders. Additionally, you will assist in facility creation and team building as per project requirements. You must have at least 11 years of experience in Medical Coding, specializing in Surgery Coding, possess proficiency in MS Word and Excel, demonstrate strong organizational skills, attention to detail, multitasking abilities, and hold a graduation degree in any stream. Mandatory certifications such as CCS, CIC, COC, or CPC are required for this role.,

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice. Sr Medical Advisor - Oncology POSITION PURPOSE: The position is responsible for the medical and scientific support, including technical advice to the Business Units and Pharmacovigilance/ Medical Information and Clinical Research teams in their assigned therapeutic areas. The position holder oversees the Medical Affairs function in India in their assigned therapeutic/product areas and cooperates with Regional Medical Affairs functions and relevant Global Medical Affairs functions. This position holder is responsible for ensuring that marketing and sales functions have appropriate medical scientific support and training (the latter in co-operation with the Training department). To enable this support, product and development project information is to be kept up to date based on internal publications and communication with regional and global Medical Affairs functions as well as based on review of pertinent scientific publications. In addition to this, the position holder is responsible for the review process of promotional materials in the respective area according to the global SOP and local laws and compliance. The tasks also include monitoring of medical marketing activities of competitors locally and worldwide and close interaction especially with regional medical affairs functions. The position holder will further support regulatory, PV/MI and CR teams in medical scientific questions and prepare and give internal (mainly marketing and sales functions) and possibly external presentations (local advisory board meetings, launch symposia and others) to enhance the medical knowledge of development projects and marketed products. This also includes interaction and relationship-building with TLs. YOUR TASKS AND RESPONSIBILITIES : Medical Marketing Provide timely and appropriate medical review of all promotional material as well as challenging promotional activities of competitors where appropriate. Support BUs in transforming medical data into marketing strategy Work closely with other members of the medical team (especially the MSLs) to support the business Build up good relationships with customers and TLs Build strong relationships with internal customers (marketing and sales) and with regional / global Medical Affairs Provide development project and product training internally to marketing and sales functions and externally to doctors Support and educate internal customers in compliance with the Country’s Code of Conduct Provide a comprehensive and proactive Medical service that encompasses, as appropriate, including Medical Support, Medical Information and Pharmacovigilance As Senior Medical Advisor, is responsible for overall medical inputs to Integrated Brand Plans of assigned therapeutic areas, provision of scientific expertise, review of promotional materials, thought leader management, speaker development and training. Takes responsibility for study development programmes of the Business units within portfolio (included local studies NIS, IIR). Identifies, initiates and completes agreed study development activities in a timely manner, be IIR responsible of local IIR. Takes responsibility for all study development activities that they are running in accordance with all applicable external and internal regulations and guidelines. Play a role as local medical expert for Global Clinical Development by providing inputs for medical queries related to trials; participate in site feasibility. Respond to all external scientific and medical queries from physicians, regulatory authorities and public alike in an accurate, transparent and convincing manner in order to position Bayer as a credible, trustworthy and professional leader in the industry. Support the Local Safety Issue and Crisis Management in collaboration with the Headquarters. Support the local Safety Management Team. Reviews all local patient support programs and other undertakings of the local organization with potential consequences on PV obligations (e.g. Market Research, Active-Online-Listening programs) to ensure Pharmacovigilance principles are applied in the interaction with patients. Develops, maintains and strengthens strategic partnership with relevant TLs, societies and associations. Act as medical contact for TL and external Medical experts. In collaboration with local marketing to develop, conduct Advisory Board meetings, Congress and Symposia. WHO YOU ARE: Certified Medical Doctor from a recognized Medical University (MBBS and MD in Pharmacology). More than three (3) years’ of experience as Medical Advisor in Oncology or Hematology Have in depth Disease Area expertise and technical knowledge in the assigned therapeutic areas. For the role is desirable: Experience in driving and managing the medical strategy for Specialty therapy area like Oncology or Hematology. Clinical trial management experience, and be able to interact authoritatively with key stakeholders and investigators. Excellent presentation and teaching skills and to represent the company in a professional manner at medical, scientific and public events. Independent, self-driven, pro-active, collaborative and customer focused. Ability to form relationships quickly and have demonstrable persuasive abilities Highly effective communicator both orally and in writing; can get ideas across one-on-in, in group settings as well as in presentations Highly organized with attention to detail Strong team player and know how to collaborate and engage many stakeholders across a large organization Solid negotiation and decision-making skills Good analytical and numerical abilities Adaptability Innovative Strategic thinking Results-oriented attitude Experience in working with MS office in a Windows environment Willing to travel Ever feel burnt out by bureaucracy? Us too. That's why we're changing the way we work- for higher productivity, faster innovation, and better results. We call it Dynamic Shared Ownership (DSO). Learn more about what DSO will mean for you in your new role here https://www.bayer.com/enfstrategyfstrategy Bayer does not charge any fees whatsoever for recruitment process. Please do not entertain such demand for payment by any individuals / entities in connection with recruitment with any Bayer Group entity(ies) worldwide under any pretext. Please don’t rely upon any unsolicited email from email addresses not ending with domain name “bayer.com” or job advertisements referring you to an email address that does not end with “bayer.com”. For checking the authenticity of such emails or advertisement you may approach us at HROP_INDIA@BAYER.COM. YOUR APPLICATION Bayer is an equal opportunity employer that strongly values fairness and respect at work. We welcome applications from all individuals, regardless of race, religion, gender, age, physical characteristics, disability, sexual orientation etc. We are committed to treating all applicants fairly and avoiding discrimination. Location: India : Maharashtra : Mumbai Division: Pharmaceuticals Reference Code: 850670 Contact Us 022-25311234

Full Time Faculty- All Non Clinical Subjects SR/AP/Associate/Professor @Medical college- Call- 7827524074 For Full Time Qualifications-DNB/Md Locations- Jaipur, Udaipur, Gaya, Dehradun, Lucknow, Bhopal. If interested, please call / WhatsApp on 7827524074 Email- hr21pathfinders@gmail.com You can share your spouse CV if He/ She is doctor. (Kindly share references if any, also circulate in your groups for Better Reach) Thanks & Regards HR Kirti PATHFINDERS

Responsible for general business development activities for a pre-clinical drug discovery & development organization providing integrated chemistry & pharmacology services Identify & connect with small/ virtual biotech companies in the United States, Europe, Japan & across the globe that can be potential customers & benefit from our unique value proposition. Create & update relevant business development databases, marketing collateral & other information documents that may aid in business development activities. Maintain CRM records, track performance metrics, & report sales forecasts & achievements. Job Type: Full-time Pay: From ₹600,000.00 per month Benefits: Paid sick time Provident Fund Schedule: Day shift Monday to Friday Work Location: In person

We require doctors for Medical Colleges & Hospitals Pan India Qualification : MD / MS / DNB (All Department ) 0-5 years of experience after MS/MD degree (any specialization) Position : Consultant , Senior Resident , Assistant Professor , Associate Professor , Professor Department : Clinical & Non Clinical Key-skills - Strong knowledge of Different Departments according to Qualification . Excellent communication skills for effective interaction with patients & colleagues. Ability to work efficiently under pressure during emergencies or critical situations Reema Call/Whatsapp : 9877677063 Email Id - weps.hrworld@gmail.com

Job Overview Provide comprehensive data management expertise (defined as efficient and quality data management products) to Data Management (DM) team to meet sponsor and company needs. Perform Clinical Data Management (CDM) Coding activities, and provide leadership either in the role of a Lead Coder or Coding Reviewer or as an individual Subject Matter Expert (SME)or lead a project as Data Operations Coordinator (DOC) or Data Team Lead (DTL)). Essential Functions Serve independently as a Clinical Data Coder, Lead Coder and/or Coding reviewer for one or more projects. Serve as an account lead, or internal or external point of contact on standalone coding studies or accounts. Manage customer relationship for the project team including active participation in coding related customer negotiation on timeline, budgetary and other issues (with guidance). Manage resource capacity for the project team. Manage delivery of coding activities and/or stand-alone coding projects through full study life-cycle. Validates/tests the coding application and programming of coding reports may also test coding related datasets, coding related edits or any coding related programming activities. Perform comprehensive data management and coding related tasks including, conducting data review and writing and resolving data clarifications. Responsible for continuous process improvement and implement process improvement initiatives by working with relevant process experts. Collaborate with customers and develop solutions and action plans for issues, escalations and road blocks. Develop and implement best practices in the team. Manage the development and implementation of new technology. Demonstrate scientific and research temperament by presenting at, or participating in local and international forums. Develop and maintain good communication and working relationship with team , client and other stakeholders. Perform other duties as directed by the study team or Manager, or meet objectives as assigned. Provide review and expert opinion in developing, revising, and maintaining core standard operating procedures and work instructions. Manage coding related project timelines with guidance from the DOC or DTL or Manager. Perform review of coded data ensuring quality and consistency of coding deliverables. Manage project timelines and quality issues and determine coding resource needs. Identify out of scope work. Serve as a back-up for the DOC or DTL or as a DOC or DTL. Perform comprehensive quality control procedures. Perform Serious Adverse Event (SAE) reconciliation activities. Qualifications Pharmacy, dental, medical, nursing, life sciences or related field qualification or educational equivalent 4 years relevant experience including clinical trials experience in a function similar to Data. Management or equivalent combination of education, training and experience. Excellent knowledge of Medical Dictionaries used for coding (e.g. MedDRA, WHODD, ICD9, etc.). Excellent knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology required for many tasks. Good project management skills related to all phases of clinical studies. Comprehensive knowledge of the data management process from study start-up through to database lock. Knowledge of operating procedures and work instructions and the ability to apply them in practice. Excellent understanding of the Drug Development Process and Data Management’s relevance to it. Comprehensive understanding of database technologies related to data management and coding. Excellent organizational, communication and leadership skills. Excellent English written and oral communication skills. Ability to work on computer systems with ease and good working knowledge of computer programs. Ability to exercise excellent attention to detail and act independently with the initiative required to resolve problems. Ability to establish and maintain effective working relationships with co-workers and managers. Understand and interpret financial management concepts. Able to present information effectively to individuals and groups. Able to make independent decisions within scope of authority and considers the impact of decisions on other groups and people. Able to motivate and lead teams to reach defined objectives. Effective team management skills including conflict resolution, delegation, and change management. Excellent interpersonal skills. Able to establish trust and collaborative relationships with customers. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

Key Responsibilities: Deliver engaging and interactive online nursing lectures through Zoom, Google Meet, or LMS platforms. Teach subjects such as Anatomy, Physiology, Medical-Surgical Nursing, Community Health, Pharmacology, and Midwifery. Prepare and share lesson plans, PPTs, notes, and recorded videos for students. Conduct online tests, quizzes, and assignments to assess student learning. Provide individual doubt-clearing sessions and feedback to students. Maintain up-to-date knowledge of nursing curriculum, guidelines, and recent clinical practices. Participate in faculty meetings, student evaluations, and academic planning. Guide students in clinical case discussions, project work, and exam preparation (GNM, BSc Nursing, Staff Nurse Exams, etc.). Qualifications: B.Sc / M.Sc in Nursing from a recognized university (specializations preferred: Medical-Surgical, Community, Obstetrics, Psychiatric). Registered Nurse (RN) with valid registration (INC or State Nursing Council). Minimum 1–3 years of teaching or clinical experience. Experience in online teaching will be an added advantage. Required Skills: Strong command of nursing subjects and current clinical practices. Proficient in using digital tools, such as MS PowerPoint, Google Classroom, Zoom, etc. Good communication and presentation skills. Ability to engage students virtually and resolve academic doubts. Fluent in English and/or Hindi (as per student requirement).

Job Title: Branch Name: Brain and Spine Medicity Qualification: B. Pharm Location: Kannur Employment Type: Full time Department: Neuro rehabilitation Dispensing Medications: Accurately dispense prescriptions as per doctors’ instructions. Ensure correct dosage, route, and duration of medication. Prescription Review: Verify prescriptions for accuracy and potential drug interactions. Clarify any inconsistencies with prescribing physicians. Patient Counseling: Educate patients on how to take their medications properly. Explain side effects, storage requirements, and precautions. Inventory Management: Maintain stock of medicines and medical supplies. Check for expiry dates and ensure proper storage conditions. Regulatory Compliance: Ensure compliance with drug laws and medical regulations. Maintain records of controlled substances and regulated drugs. Coordination with Medical Staff: Collaborate with doctors and nurses for medication plans. Advise on substitutions, interactions, or new drug updates. Billing & Documentation: Manage billing for dispensed medications. Maintain accurate logs of prescriptions and dispensed drugs. Quality Control: Monitor for counterfeit or substandard drugs. Ensure all medications meet safety and quality standards. Requirements In-depth knowledge of pharmacology and therapeutics Attention to detail and accuracy Strong communication and counseling skills Inventory and supply chain management Problem-solving and decision-making Familiarity with drug regulations and compliance Basic computer skills (for billing and e-prescriptions) Ethical responsibility and patient-centered care

DARADIA PAIN HOSPITAL is looking for Pharmacist to join our dynamic team and embark on a rewarding career journey Reviewing and interpreting prescription ordersPreparing and dispensing medicationsAdvising patients on the safe and effective use of their medications, including potential side effects and interactionsMonitoring patients for adverse reactions and ensuring that any necessary changes to their medication regimen are made in a timely mannerKeeping accurate and up-to-date records of patients' medication history and any adverse reactionsCollaborating with other healthcare professionals to provide comprehensive care to patientsStaying current on developments in the field of pharmacology and medication therapy

Urgent vacancies for Faculties Senior Residant with good experience in medical college at a medical college in jaipur Salary as per industry Norms,

Teaching & training Undergraduate (MBBS) Medical students including Interns/ Postgraduate Medical students so as to achieve the Educational Objectives i.e. to develop their knowledge, skills & attitude.Teach residents and students patient care unit

Leadership & Strategy Provide leadership and direction for all pharmacy services and staff. Develop and implement departmental goals aligned with organizational strategy. Promote a culture of safety, excellence, and continuous improvement. Clinical Governance & Compliance Ensure adherence to national and institutional regulations (e.g., FDA, MHRA, GPhC, NABH). Oversee medication safety, formulary management, and pharmacovigilance programs. Lead audits, quality assurance initiatives, and risk mitigation strategies. Operational Management Oversee procurement, inventory, and distribution of medications. Optimize pharmacy workflows, staffing, and use of technology. Ensure availability of essential drugs and rational drug use. Financial & Resource Management Develop and manage department budgets. Monitor drug expenditure and implement cost-control measures. Lead contract negotiations with suppliers and vendors. Education & Research (if in an academic or teaching hospital setting) Supervise and mentor pharmacy staff, students, and residents. Oversee continuing education and professional development programs. Facilitate academic teaching, curriculum development, and research initiatives. Collaboration & Communication Liaise with clinicians, nursing, and administrative departments to ensure integrated care. Serve as the departments representative in institutional committees and external bodies. Engage patients and stakeholders in medication-related education and decisions.

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Sr Associate IS Analyst What you will do Let’s do this. Let’s change the world. In this vital role you will be part of the Product Team responsible for completing the digital roadmap strategy, ongoing design, development, management, and optimization of Amgen Operation’s Electronic Lab Notebook (ELN) and Instrument Data Acquisition Platform. The ideal candidate will have an excellent grasp of the technology for Lab applications with a passion for fostering innovation and excellence in the biotechnology industry. Strong preference will be given to candidates with experience working in ELN Applications, Enterprise Application Integration, end-to-end data and process harmonization, as well as handling the seamless integration of Lab Instrument data to various enterprise business applications. This individual will also be engaging with key vendors and partners with collaborators orchestrating the implementation of solutions that enable next generation lab processes including simulations, machine learning and knowledge management. The ideal candidate will have a solid understanding of the end-to-end software development lifecycle, technical product ownership, business analysis, Scaled Agile framework, coupled with leadership and transformation experience. This role demands the ability to drive and deliver against key organizational critical initiatives, develop a collaborative environment, and deliver high-quality results in a matrixed organizational structure. Roles & Responsibilities: Develop and Maintain solutions for Operations Enterprise Lab Information Management solutions, including Biovia’s Holistic Lab ELN Platform. Support alignment of business processes with Holistic Lab ELN, Product Life Cycle Management (PLM), and Big Data technology capabilities by working with multi-functional representatives across Operations and sites. Develop and implement business process improvements to consistently enhance efficiency and effectiveness. Monitor, solve, and resolve issues related to case intake and case processing across multiple systems. Work closely with internal teams, external vendors, and business partners to address dependencies and resolve bottlenecks for critical issues Ownership in the development of test plans, scenarios to ensure robust validation of system updates, patches and new features Perform regression & functional testing to verify the changes do not negatively impact existing system functionality Work with other Amgen infrastructure teams to stand up various infrastructure environments (DEV/TEST/PROD) in the cloud or on-prem What we expect of you We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications: Master’s degree/Bachelor's degree with 5- 9 years of Life Science/Biotechnology/Pharmacology/Information Systems experience. Functional Skills: Must-Have Skills: Experience in user requirements and acceptance criteria in agile project management systems such as JIRA and identification and execution of scripts. Good communication skills and the ability to work with Product Managers and business collaborators to define scope and value for new developments Hands-on experience with the ITIL framework and methodologies like (Scrum). Knowledge of SDLC process, including requirements, design, testing, data analysis, change control Proven leadership skills with the ability to multitask and lead simultaneous software/hardware lifecycle projects Partner with vendors and other team members to troubleshoot problems, test new software versions, and secure long-term solutions for Platform roadmap Good-to-Have Skills: Hands-on experience in HP ALM, JIRA, Confluence, document management systems (e.g., CDOCs) and Service Now. Experience in management of test plans, test protocols, defect management, and requirements traceability matrix Experience of Continuous Integration and Continuous Delivery methodology Ability to work independently, excellent problem solving and professional written communications skills. Strong customer focus with ability to work closely with business collaborators to advance their organizational goals Experience working in a globally distributed enterprise application platform within the Lab solution landscape – including ELN, inventory management, MES and scientific analysis tools Worked in a highly regulated pharmaceutical or technology organization, with the ability to ensure compliance with industry regulations and standard methodologies for GxP software validation. Soft Skills: Excellent leadership and team management skills. Strong transformation and change management experience. Ability to work effectively with global, virtual teams. Excellent analytical and troubleshooting skills. Ability to manage multiple priorities successfully. Strong presentation and public speaking skills. Strong verbal and written communication skills. High degree of initiative and self-motivation. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Eligibility Criteria: Educational Qualification: B.Pharmacy with First Class (Mandatory) M.Pharmacy in any specialization (Desirable) Must be registered with the State Pharmacy Council . Prior teaching or industrial experience of atleast 3 years will be an added advantage. Job Description: We are inviting applications for the post of Lecturer to teach Diploma in Pharmacy (D.Pharm) students. The candidate should possess sound knowledge of pharmacy subjects and be passionate about delivering quality education in both theory and practical components. Key Responsibilities: Deliver lectures in core pharmacy subjects such as Pharmaceutics, Pharmacology, Pharmacognosy, Pharmaceutical Chemistry, and Health Education . Conduct and supervise practical/laboratory sessions as per PCI norms. Prepare lesson plans, teaching materials, and question papers. Assess students’ academic progress through internal tests and assignments. Guide students in academic and career matters. Maintain records such as attendance, internal marks, and lab files. Participate in co-curricular, examination, and administrative duties as assigned. Desired Skills: Strong subject knowledge and presentation skills. Good communication in English, Hindi, and Punjabi (as needed). Classroom management and student engagement skills. Basic computer proficiency (MS Office, Google Workspace). Salary: As per norms and experience Job Types: Full-time, Permanent, Fresher Pay: ₹15,600.00 - ₹21,600.00 per month Work Location: In person

Key Responsibilities: Serve as a technical liaison between engineering, sales, and medical clients to support biomedical product and pharmaceutical-related negotiations. Evaluate biomedical devices and solutions in relation to drug delivery, compatibility with pharmaceuticals, or combined device-drug systems. Participate in negotiations and product positioning with hospitals, procurement teams, and pharmaceutical partners. Provide scientific and technical input during product discussions, focusing on both device and medicine aspects. Collaborate with R&D, Quality, and Regulatory teams to ensure product compliance and relevance to clinical needs. Conduct market and competitor analysis on medical devices and pharmaceutical solutions to enhance negotiation outcomes. Support the customization of products to meet client needs in clinical, pharmaceutical, or hospital environments. Deliver technical presentations, training, and documentation related to products and drug-device integration. Requirements: Bachelor’s or Master’s degree in Biomedical Engineering, Pharmaceutical Sciences, or related field. 3–5 years of experience in medical devices, pharmaceuticals, or a healthcare-focused technical role. Proven experience in product negotiation or technical sales involving biomedical products and/or medicines. Solid understanding of pharmacology, drug-device combinations, and regulatory standards. Strong interpersonal and communication skills, with the ability to simplify complex information. Proficiency in CRM tools, Microsoft Office, and technical documentation software. Job Type: Full-time Pay: ₹11,000.00 - ₹25,000.00 per month Work Location: In person

Should have knowledge in Clinical Data Management Should have good knowledge in edit checks crf design SAE Reconcilation crf annotation Clinical Data Management Trained Candidates Only Eligible Required Candidate profile Strong understanding of clinical data management and E2b Guidelines Excellent clinical assessment and Communication Skills

Chandigarh Group of Colleges, Landran is inviting applications for the position of Professor in the Pharmacy Department with specialization in Pharmacology and Pharmacy Practice . We are seeking dynamic, experienced, and research-oriented professionals committed to academic excellence and innovative teaching. Specializations Required: Pharmacology Pharmacy Practice Qualification & Experience: Ph.D. in the relevant discipline is mandatory First Class in B.Pharm and M.Pharm Minimum 12 years of teaching/research/industry experience out of which at least 8 years should be at the level of Associate Professor Proven record of published research papers, patents, projects preferred Key Responsibilities: Delivering lectures and mentoring undergraduate and postgraduate students Conducting research, guiding PhD scholars, and publishing in reputed journals Designing curriculum and improving academic processes Active participation in departmental and institutional initiatives Organizing and attending national/international conferences, workshops, and seminars Interested candidates may share their updated resume at ankita.hr@cgc.edu.in or contact/DM 9875939971 . Kindly mention the subject line as: Application for Professor Pharmacy (Pharmacology / Pharmacy Practice)”

Company Description CT Group of Institutions is a premier educational group dedicated to excellence in education and life. Featuring a vast array of institutions from pre-schools to postgraduate programs, the group boasts world-class infrastructure, Wi-Fi enabled campuses, well-equipped libraries, advanced laboratories, and support from experienced academicians. CT Group offers a conducive environment for education across various disciplines, including Engineering, Architecture, Management, Pharmacy, IT, Hotel Management, and Fashion Designing, setting benchmarks comparable to the best in the world. Role Description This is a full-time, on-site role located in Jalandhar for an Assistant Professor of Pharmacology at CT Group of Institutions. The Assistant Professor will be responsible for teaching undergraduate and graduate students in pharmacology. Duties include preparing and delivering lectures, conducting research, guiding student projects and research, assessing student performance, participating in faculty meetings and committees, and keeping up with advancements in the field to integrate into teaching. Qualifications Knowledge of Pharmacology and related subjects Experience in teaching, preparing lectures, and managing classroom activities Ability to conduct research and guide student projects Strong communication, presentation, and interpersonal skills Proficiency in using educational technologies and laboratory equipment Commitment to continuous professional development and staying updated with advancements in Pharmacology Ph.D. in Pharmacology or a related field, or a Master’s degree with significant teaching and research experience Experience in academic administration and faculty collaboration is a plus

Job Description: Associate Professor / Professor (Pharmacy) Institution Rama University, Kanpur, a premier institute recognized by the University Grants Commission (UGC), invites applications for the position of Associate Professor / Professor in the Department of Pharmacy. Position Overview The Associate Professor / Professor will contribute to the academic and research mission of the Department of Pharmacy, with expertise in Pharmacology , Pharmacognosy , and Pharmaceutics . The role involves delivering high-quality teaching, mentoring students, conducting innovative research, and contributing to institutional development in alignment with UGC guidelines. Key Responsibilities Teaching and Academic Duties Develop and deliver undergraduate and postgraduate courses in Pharmacology, Pharmacognosy, and Pharmaceutics. Design innovative curricula, teaching materials, and assessment methods to enhance student learning outcomes. Supervise and mentor students in academic projects, internships, and dissertations. Provide academic counseling and support to students, fostering their professional development. Research and Scholarly Activities Conduct high-impact research in Pharmacy, leading to publications in peer-reviewed journals of national and international repute. Secure research grants from funding agencies such as UGC, AICTE, DST, or other relevant bodies. Guide Ph.D. scholars and postgraduate students in their research projects. Present research findings at national and international conferences and seminars. Contribute to interdisciplinary research initiatives within the institution. Administrative and Institutional Contributions Participate in departmental and institutional committees as per UGC norms. Contribute to accreditation processes, curriculum development, and quality assurance initiatives. Engage in outreach activities, including industry collaborations, workshops, and community service programs. Assist in organizing seminars, conferences, and continuing education programs in Pharmacy. Qualifications and Experience As per UGC guidelines for Associate Professor / Professor positions: Educational Qualifications : Ph.D. in Pharmacy with specialization in Pharmacology, Pharmacognosy, or Pharmaceutics from a recognized institution. Master’s degree in Pharmacy (M.Pharm.) in the relevant specialization with a minimum of 55% marks (or equivalent grade) from a recognized university. Bachelor’s degree in Pharmacy (B.Pharm.) from a recognized institution. Experience : For Associate Professor : A minimum of 8 years of teaching and/or research experience in an academic/research position equivalent to Assistant Professor, with at least 2 years post-Ph.D. experience. A minimum of 7 peer-reviewed publications in reputed journals as per UGC norms. For Professor : A minimum of 10 years of teaching and/or research experience, with at least 3 years as an Associate Professor. A minimum of 10 peer-reviewed publications in reputed journals, with evidence of having successfully guided doctoral candidates. Research Requirements : Demonstrated record of high-quality research with publications in Scopus/Web of Science-indexed journals. Experience in securing and managing research grants is highly desirable. Proven ability to guide Ph.D. and postgraduate research projects. Desirable Skills : Strong teaching pedagogy with expertise in modern teaching methodologies, including e-learning and experiential learning. Proficiency in laboratory techniques relevant to Pharmacology, Pharmacognosy, or Pharmaceutics. Excellent communication, interpersonal, and leadership skills. Commitment to fostering an inclusive and collaborative academic environment. Additional Requirements Compliance with UGC regulations (2018 or as amended) for the appointment of Associate Professor / Professor. Evidence of contribution to institutional development, such as curriculum design, accreditation, or industry-academia collaborations. Active participation in professional bodies or associations related to Pharmacy.

Department : Faculty of Pharmaceutical Sciences Institution : Rama University, Mandhana,Kanpur Reports to : Dean, Faculty of Pharmacy Position Type : Full-Time, Permanent About Rama University Rama University is one of North India’s largest educational groups, known for its emphasis on academic excellence, research, innovation, and holistic student development. The Faculty of Pharmaceutical Sciences is a center of excellence offering undergraduate, postgraduate, and doctoral programs in Pharmacy. Job Purpose To lead and contribute to teaching, research, and academic leadership within the Department of Pharmacy, while actively participating in curriculum development, mentoring students, and driving research initiatives aligned with the university’s vision. Key Responsibilities : Academic & Teaching Deliver high-quality lectures to undergraduate and postgraduate pharmacy students. Supervise doctoral and postgraduate research scholars. Develop innovative teaching methodologies and learning materials. Ensure curriculum is aligned with current pharmaceutical industry trends and regulatory requirements (e.g., PCI, AICTE, UGC). Research & Publications Undertake original research and contribute to the institution’s publication output. Secure external funding for research projects. Publish research in high-impact, peer-reviewed journals. Represent the university at national and international academic conferences. Administrative & Leadership Lead academic committees and participate in departmental planning and review. Mentor junior faculty and assist in their professional development. Participate in accreditation, ranking processes, and quality assurance activities. Collaborate with pharmaceutical industry partners and regulatory bodies. Qualifications & Experience : Ph.D. in Pharmacy or Pharmaceutical Sciences (essential) M.Pharm with specialization in any relevant branch (e.g., Pharmaceutics, Pharmacology, Pharmaceutical Chemistry, etc.) Minimum 10 years of teaching and research experience in a recognized institution, including at least 5 years as Associate Professor Proven record of high-quality research, publications (minimum 10 in Scopus/Web of Science indexed journals), and academic leadership Sound knowledge of pharmacy education regulations (PCI norms) Preferred Skills : Excellent communication and leadership skills Familiarity with modern teaching aids and LMS platforms Strong research acumen and project management abilities Industry exposure and connections preferred Compensation & Benefits Competitive salary as per UGC/PCI norms Additional research incentives, housing allowance, health benefits, and professional development support. How to Apply Interested candidates should send a detailed CV, cover letter, list of publications, and two professional references to: Email : dristitiwari.hr@ramauniversity.ac.in Subject Line : Application for Professor – Pharmacy

Senior Drug Safety Associate Category: Reg Affairs & Safety Pharmacovigilance Location: Bangalore, Karnataka, IN Novo Nordisk Global Business Services Senior Drug Safety Associate Are you driven by challenges and energized by a fast-paced, dynamic environment? Do you thrive in a role where strategic alignment, stakeholder collaboration, and continuous improvement are key to success? We are looking for a Senior Drug Safety Associate to join our growing team in an international setting. In this pivotal role, you will work closely with cross-functional teams to ensure the highest standards of patient safety and regulatory compliance throughout the drug development lifecycle. Apply now and become part of a collaborative, forward-thinking environment where your expertise truly makes an impact. About The Department: Global Patient Safety Bangalore (GPS-BLR) was set up in 2010 as one of the hubs for safety case processing. We handle case processing and medical review of Individual Case Safety Reports from different sources (spontaneous, literature, solicited and clinical trials). We are additionally engaged in safety surveillance, safety medical writing, safety report submission, training, quality control of ICSRs, Argus configuration and maintenance, information technology quality assurance, training co-ordination and literature surveillance activities, including medical literature monitoring. The Position : As a Senior Drug Safety Associate you will be responsible for the comprehensive management of both serious and non-serious adverse event reports from various sources. Your core duties will include initial medical evaluation, accurate case entry, and verification of safety data within the Novo Nordisk safety database (Argus). You will ensure consistent and precise coding using MedDRA, evaluate causality, seriousness, and listedness, and ensure that case narratives reflect accurate and relevant safety information. You will also assess the need for follow-up, issue appropriate queries in the EDC system and/or to affiliates, and actively participate in weekly literature surveillance activities. Responsible to conduct medical evaluation, coding, and case processing of serious and non-serious adverse events in compliance with GxP and regulatory requirements, using Argus and MedDRA. Liaise with global affiliates, partners, and internal stakeholders to clarify safety data, ensure timely follow-up, manage local literature, and support compliance activities. Collaborate with Safety Reporting and IT teams for data retrieval, custom reporting, and to assess system/process changes impacting pharmacovigilance operations. Ensure Support system optimization and data integrity, collaborating with Safety Reporting and IT for custom data retrieval, reporting, and assessing the impact of system or process changes on pharmacovigilance activities. Mentor and train colleagues, act as a buddy, and proactively contribute to continuous process improvement across global safety functions. Qualifications: We are looking for a candidate who can bring the following skills and experience to the role: Graduation and/or post-graduation in Life Sciences (e.g., Medicine, Pharmacy, Biotechnology, Nursing). Minimum experience of 4 years in processing of Individual case safety reports (ICSR). Experience in mentoring, training, quality trend analysis will be preferred. Sound knowledge and hands-on experience in Pharmacovigilance and adverse event reporting processes which includes triage/intake, data entry, Quality review within various case types. Knowledge of safety databases like Argus and familiarity with MedDRA coding. Strong understanding of medical terminology, clinical pharmacology, and global PV regulatory requirements. Familiarity with GxP as well as GDPR standards and compliance expectations within a pharmaceutical setting. Proficient in MS Windows applications, including Excel, Word, Outlook, and PowerPoint. Excellent written and verbal communication skills in English, with a strong ability to convey medical and scientific concepts clearly. Proven ability to work within cross-functional teams and collaborate across global departments and affiliates. Demonstrated ability to foresee and assess the impact of system/process changes on safety operations. Solid understanding of Novo Nordisk products, including mechanisms of action, safety profiles, and patient populations. Experience working in a pharmaceutical company or a similar organization. Working at Novo Nordisk Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 72,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing. Contact To submit your application, please upload your CV online (click on Apply and follow the instructions). Deadline 29th July 2025. Disclaimer It has been brought to our attention that there have recently been instances of fraudulent job offers, purporting to be from Novo Nordisk and/or its affiliate companies. The individuals or organizations sending these false employment offers may pose as a Novo Nordisk recruiter or representative and request personal information, purchasing of equipment or funds to further the recruitment process or offer paid trainings. Be advised that Novo Nordisk does not extend unsolicited employment offers. Furthermore, Novo Nordisk does not charge prospective employees with fees or make requests for funding as a part of the recruitment process. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.

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 expertise will be pivotal in validating these models to a level suitable for Regulatory submissions and influencing the design of clinical trials. Furthermore, effective communication internally and externally on topics related to PBPK clinical DDI, pediatric, and other specific populations predictions will be essential. To excel in this role, you should possess knowledge of pharmacokinetics, Model-Informed Drug Development (MIDD), and have demonstrated experience in translational development, preferably with 0-4 years of drug development experience focusing on PBPK modeling. Additionally, familiarity with pharmacology, drug targets, and core disease areas is required. A Ph.D. degree or equivalent (M.Sc./Pharm.D.) with relevant experience is preferred. Proficiency in spoken and written English, along with training and experience in PBPK and relevant software such as SimCYP, GastroPlus, PK-Sim, and Phoenix WinNonlin, is necessary. Desirable skills include a strong scientific publishing reputation in the field of DMPK/Clinical Pharmacology and experience in early and late-stage drug development. By being a part of our diverse and inclusive team, you will have the opportunity to contribute to groundbreaking discoveries that have the potential to transform lives. If you are ready to make a significant impact in the field of clinical PBPK modeling, we invite you to apply now and embark on this exciting journey with us at AstraZeneca.,

Job Description This role is responsible for providing technical support to the concerned Sales teams across Bihar, Jharkhand, Assam and West Bengal, by conducting technical trainings related to animal health and products to field sales personnel , organizing and participating in the technical seminars to field veterinarians & customers along with Sales team, attending the customer complaints, meeting Veterinary professionals of field and colleges for sharing of technical inputs, coordinating with Veterinary Service Dept. Corporate and Diagnostic laboratory in disease surveillance, customer requirements and field trials Our Veterinary team use their scientific background to provide technical expertise and education to our customers, sales and marketing teams. With a deep knowledge of pharmacology and animal health we engage scientific exchange with external experts and industry leaders ensuring the scientific value of our animal health portfolio is understood. Responsibilities Primary responsibilities include: Providing Technical Services to customers in assigned geography (these services include on-site customer visits along with Sales Team & off-side telephonic support as well) and executing a comprehensive Tech service plan for maximizing Organizational goals. Customer Meetings: Meet customers in a group to create awareness about relevant scientific practices and advancements with the objective to become a partner of choice among customers. Technical Upgradation of the Sales team in assigned geography: Staying ahead of curve for recent technical development in Ruminant Industry and preparing internal competencies to provide customer support. Supervising Local Clinical Trials and Market support studies under the guidance of Sr. Tech Manager. Publication of Clinical Trials & Market Support Study Outcomes in relevant peer-reviewed Scientific Journals Supervise and provide timely and effective technical materials which maximize selling efforts. Collaboration with relevant Technical & Veterinary Education institutes in assigned geographies to further improve our image as Science Driven Organization Any other relevant task which can help in improving business. Rol Technical support to Pharmacovigilance team P.S: The Head quarter for this role can be either Patna or Kolkata and this profile requires extensive travelling Qualifications & Skills Degree in Veterinary Sciences 2-3 years of field experience to handle all field situations and provide technical solutions to customer needs. Freshers and Women candidates are also welcome for this opening. Our Animal Health Division is a trusted global leader in veterinary medicine, dedicated to preserving and improving health, well-being, and performance of animals and the people who care for them. We are a global team of professionals working together to make a positive difference in animal care and the world’s food supply and have a deep sense of responsibility towards our customers, consumers, animals, society, and our planet. Through our commitment to The Science of Healthier Animals®, we offer veterinarians, farmers, pet owners and governments one of the widest ranges of veterinary pharmaceuticals, vaccines and health management solutions and services as well as an extensive suite of digitally connected identification, traceability and monitoring products. We invest in dynamic and comprehensive R&D resources and a modern, global supply chain. We are present in more than 50 countries, while our products are available in some 150 markets. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation: VISA Sponsorship Travel Requirements: Flexible Work Arrangements Not Applicable Shift Valid Driving License: Hazardous Material(s) Required Skills: Preferred Skills Job Posting End Date: 06/30/2025 A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID: R301402

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 hospital policies Conduct medication reconciliation during patient transitions of care Participate in clinical rounds and provide drug information and therapeutic recommendations to healthcare teams Maintain accurate and updated patient medication records Assist in formulary management and participate in drug utilization reviews and audits Provide training and guidance to pharmacy staff, students, or residents Ask ChatGPT