1619 Pharmacology Jobs

Company Description Ribosome Research Centre Pvt. Ltd. is a Global Contract Research Organization offering a comprehensive range of In Vitro & In Vivo Preclinical Services. Our services include Analytical Chemistry, Microbiology Services for Pharma, Medical Devices, Agrochemical, Specialty Chemicals, Cosmetics, and AYUSH Products. We are dedicated to providing a one-stop solution for all your research and development needs. Role Description This is a full-time, on-site role for an OECD GLP QA Auditor located in Kim. The OECD GLP QA Auditor will be responsible for conducting study based/process based/facility based insand audits to ensure compliance with Good Laboratory Practices (GLP). The auditor will also be responsible to review quality tools like deviation, CAPA, change control etc. To be responsible for facing sponsor and regulatory inspection like OECD GLP, CDSCO, NABL etc. Ensuring compliance with company standards and regulatory requirements will be a core part of the role. Qualifications M.Pharm preferably in Pharmacology, M.Sc in Zoology. Experience in Quality Auditing and Quality Assurance Strong knowledge of Auditing principles and practices Excellent attention to detail and analytical skills Ability to work independently and on-site OECD GLP experience is compulsory

Urgent Vacancies for Teaching Faculties in a Medical College & Hospital in Jodhpur Salary as per industry Norms.

Job Summary: Registered Pharmacist A Pharmacist is a healthcare professional responsible for dispensing medications, providing patient counseling, ensuring drug safety, and collaborating with healthcare providers to optimize treatment outcomes. They play a critical role in patient care by verifying prescriptions, advising on proper medication use, and promoting health and wellness. DIRECT WALK IN INTERVIEW : 15th & 16th September 2025 . Venue : WELLCAZA SCHOOL OF HEALTH SCIENCES . Edappally Raghavan Pillai Road, Elamakkara, Kochi, Ernakulam, Ernakulam District, Kerala 682026, India. HRD Contact number : +91 86061 25413 (Interview related enquiry only will be acknowledged) Key Responsibilities:1. Medication Dispensing & Management: Accurately interpret and fill prescriptions. Verify dosage, drug interactions, and patient allergies. Ensure compliance with legal and regulatory requirements (e.g., FDA, DEA). Manage inventory, including controlled substances. 2. Collaboration & Healthcare Support: Work with doctors, nurses, to optimize treatment plans. Clarify prescription issues with prescribers when needed. Participate in multidisciplinary healthcare teams. 3. Pharmacy Operations & Compliance: Maintain accurate patient records and pharmacy documentation. Follow safety protocols and infection control measures. Supervise pharmacy technicians and support staff. Stay updated on new drugs, guidelines, and industry trends. Qualifications & Skills: Education: DPharm, BPharm , Doctor of Pharmacy (Pharm.D.) degree from an PCI accredited institution. Licensure: Valid state pharmacist license (must be in good standing). Experience: Previous retail, hospital, or clinical pharmacy experience preferred. Skills: Strong attention to detail. Excellent communication and interpersonal skills. Proficiency in pharmacy software and EHR systems. Knowledge of pharmacology, drug interactions, and compounding. Work Environment: Retail pharmacies, hospitals, clinics, or pharmaceutical companies. May require standing for long hours and handling emergencies. Job Type: Full-time Pay: ₹10,000.00 - ₹20,000.00 per month Work Location: In person

Job Title: Area Medical Advisor, Vaccines Position Summary: This role offers an exciting opportunity to make a meaningful impact on public health. You will provide scientific and medical expertise to support healthcare professionals and ensure accurate medical information is shared. Collaboration is key—you’ll work closely with cross-functional teams and external experts to drive scientific engagement. We value candidates who are proactive, detail-oriented, and passionate about improving health outcomes. Responsibilities: Build and maintain strong relationships with healthcare professionals and external experts. Deliver scientific presentations at medical education events, workshops, and conferences. Support the development and execution of medical strategies aligned with business goals. Stay updated on the latest scientific research and ensure accurate, compliant communication. Provide medical input for research feasibility assessments and field studies. Contribute to pharmacovigilance activities to ensure patient safety. Qualifications/Skills: Basic: MBBS or equivalent medical degree. Strong communication skills in English and local language. Experience presenting scientific topics in professional settings. Understanding of scientific methods and experimental design. 2–5 years of experience in the pharmaceutical, vaccines, or biologicals industry. Preferred: Postgraduate qualification in Public Health, Pharmacology, or related fields. Research experience in immunology, epidemiology, or infectious diseases. Familiarity with ICH-GCP principles and industry codes. Proven ability to build relationships with healthcare professionals and key opinion leaders. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way. GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable. If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing askus@gsk.com, so that we can confirm to you if the job is genuine.

Job Purpose: Provide scientific and technical expertise of the highest standards for local medical information, including interactions with Key External Experts (KEEs) and Key Opinion Leaders (KOLs) Provide medical and scientific input and information for business strategy for the region. Key Responsibilities : Develop and sustain credible networking with appropriate Health Care Practitioners (HCPs) Plan, facilitate and conduct CMEs, symposia, trainings, workshops, scientific meetings, speaker tours, and other product specific campaigns and deliver scientific presentations with consistent messages for key products at these meetings, as required. Support and deliver scientific presentations with consistent “on label” messages at medical education meetings. Understand principles of and support Scientific Engagement (SE) activities as per Medical Plans. Have clarity in understanding on Scientific Engagements and Promotional Code. Become an expert in oncology where GSK have brands and support associated activities related to those brands. Be updated on scientific knowledge on oncology; GSK molecules and its PI to ensure its ‘On Label’ communications on various platforms. Support in feasibility assessment of potential research sites, develop concept notes, proposals, budgets, data collection and monitoring tools for field studies. Provide medical inputs into development and execution of brand strategy. Pharmacovigilance: Support Named Safety contact in strengthening of oncology Pharmacovigilance; ensure self-learning. Knowledge/ Education / Previous Experience Required A. Educational Background :- Minimum Level of Education - MBBS with post graduate qualification Preferred Level of Education - Post graduate qualification in Pharmacology / Public Health Why is this Level of Education Preferred - To interact with specialized HCPs B. Job-Related Experience:- Minimum Level of Job-Related Experience required Excellent written and oral communication skills in English, local language Experience of presenting scientific topics at different settings A sound understanding of the principles and practice of ICH-GCP and internal SOPs. Well-demonstrated ability to understand scientific methods and experimental design. 1-2 years in the pharmaceutical industry preferably in the oncology therapy area. C. Other Job-Related Skills/Background:- General Competencies Presentation skills at Scientific meetings Communication skills, both verbal and written Technical writing skills Keep up to date with new developments Ability to provide and receive constructive feedback Build and maintain relationships with colleagues Share knowledge with other team members Work as part of a team to reach common goals Deliver creative ideas for continuous improvement Develop good relationships with key opinion leaders Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way. GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable. If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing askus@gsk.com, so that we can confirm to you if the job is genuine.

call 9176256100 Willing to work in rotational shift 1 Dispensing medications, managing inventory, and maintaining records. 2. Ensure compliance with hospital policies, regulations, and accreditation Accurately dispense prescription medications to patients. Review prescriptions for accuracy, appropriateness, and potential drug interactions. Counsel patients on the correct use of prescribed and over-the-counter medications. Monitor patient medication therapies and provide recommendations for adjustments when necessary. 2. Develop and implement performance improvement plans to ensure excellent patient care and customer service. 3. Medication Safety and Quality: 1. Develop and implement medication safety initiatives to minimize errors and adverse events. 2. Monitor and report medication errors, near misses, and adverse events. 4. Inventory Management and Financials: 1. Manage pharmacy inventory, including purchasing, stocking, and controlling medications and supplies. 5. Skills and Knowledge: 1. Strong knowledge of pharmacology, therapeutics, and pharmacy practice. 2. Excellent communication, leadership, and management skills. 3. Ability to work effectively in a fast-paced environment and prioritize tasks. 1. Inventory Management: 1. Oversee the receipt, storage, and issuance of pharmacy supplies and medications. 2. Maintain accurate inventory records and perform regular stock checks. 3. Ensure adequate stock levels and minimize stockouts. 2. Customer Service: 1. Provide excellent customer service to healthcare staff, patients, and visitors. 2. Respond to queries and resolve issues promptly. 3. Ensure that customer needs are met efficiently and effectively. 3. Compliance and Regulatory Affairs: 1. Maintain accurate records and documentation. 2. Participate in audits and inspections. 4. Team Management: 1. Supervise and train pharmacy store staff. 2. Ensure that staff are aware of and comply with pharmacy policies and procedures. 5. Skills and Knowledge: 1. Excellent communication, interpersonal, and problem-solving skills. 2. Ability to work effectively in a fast-paced environment and prioritize tasks. Job Type: Full-time Pay: From ₹20,000.00 per month Benefits: Health insurance Paid time off Provident Fund Work Location: In person

Hiring SR/AP, Professor Pediatrician Medicine Surgeon Orthopedic Gynecology Emergency Anesthesia Community Radiology Pharmacology Forensic Biochemistry Anatomy Physiology Microbiology In Medical College in Allahabad & Varanasi MBBS & MD 8423159700

Job Summary: Registered Pharmacist A Pharmacist is a healthcare professional responsible for dispensing medications, providing patient counseling, ensuring drug safety, and collaborating with healthcare providers to optimize treatment outcomes. They play a critical role in patient care by verifying prescriptions, advising on proper medication use, and promoting health and wellness. DIRECT WALK IN INTERVIEW : 15th & 16th September 2025 . Venue : WELLCAZA SCHOOL OF HEALTH SCIENCES . Edappally Raghavan Pillai Road, Elamakkara, Kochi, Ernakulam, Ernakulam District, Kerala 682026, India. HRD Contact number : +91 86061 25413 (Interview related enquiry only will be acknowledged) Key Responsibilities:1. Medication Dispensing & Management: Accurately interpret and fill prescriptions. Verify dosage, drug interactions, and patient allergies. Ensure compliance with legal and regulatory requirements (e.g., FDA, DEA). Manage inventory, including controlled substances. 2. Collaboration & Healthcare Support: Work with doctors, nurses, to optimize treatment plans. Clarify prescription issues with prescribers when needed. Participate in multidisciplinary healthcare teams. 3. Pharmacy Operations & Compliance: Maintain accurate patient records and pharmacy documentation. Follow safety protocols and infection control measures. Supervise pharmacy technicians and support staff. Stay updated on new drugs, guidelines, and industry trends. Qualifications & Skills: Education: DPharm, BPharm , Doctor of Pharmacy (Pharm.D.) degree from an PCI accredited institution. Licensure: Valid state pharmacist license (must be in good standing). Experience: Previous retail, hospital, or clinical pharmacy experience preferred. Skills: Strong attention to detail. Excellent communication and interpersonal skills. Proficiency in pharmacy software and EHR systems. Knowledge of pharmacology, drug interactions, and compounding. Work Environment: Retail pharmacies, hospitals, clinics, or pharmaceutical companies. May require standing for long hours and handling emergencies. Job Type: Full-time Pay: ₹10,000.00 - ₹20,000.00 per month Work Location: In person

Overview Cactus Life Sciences is a remote-first organization, and we embrace an "accelerate from anywhere culture". You may be required to travel to our Mumbai office based on business requirements or for company/team events. If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you. Responsibilities Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client needs with excellent attention to detail under the guidance of the scientific leads. Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders, including authors, reviewers, and key opinion leaders across therapeutic areas - learning to anticipate their needs. Effectively and proactively communicate with team members, authors/faculty, clients, and vendors. Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives. Attend client and other external meetings and support senior team members as needed. Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans. Ensure all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date. Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines. Share best practices and client preferences, thereby contributing to skill development within the medical communications team. Qualifications And Prerequisites 1-3 years of experience in relevant fields of scientific writing. PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD with a good understanding of clinical research and medical communication. Should have experience working on publications. Experience working on gastric cancer publications would be preferable. Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills. Excellent communication skills, especially with the clients. Ability to adapt writing style to different materials and target audiences. Basic knowledge of biostatistics. Literature reviewing and evaluation capabilities. Very good working knowledge of MS Office. Application Process Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds. For this role, the process starts with a Technical Interview with the hiring managers, followed by a Technical Assessment, where candidates will have agreed upon timeline to complete the task. The final round will be the HR Interview. All interactions will be conducted virtually via MS Teams. Equal Opportunity Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic. Accelerating from Anywhere As a remote-first organization, these are essential attributes we look for in all our candidates. Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently. Documenting work that brings everyone on the same page. Maturity to choose between synchronous and asynchronous collaboration. Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status. About CACTUS At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do. Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

MAIN PURPOSE OF ROLE Summarize the main purpose of the role. Specialist professional individual contributor with comprehensive knowledge in the area of Medical Affairs. Ability to execute highly complex or specialized projects. Adapts precedent and may make significant departures from traditional approaches to develop solutions. Main Responsibilities As the Specialist in the Medical Affairs Sub-Function, considered as highly experienced and knowledgeable resource within the organization in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. Contributes to implementation of clinical protocols, and facilitates completion of final reports. Recruits clinical investigators and negotiates study design and costs. Responsible for directing human clinical trials, phases III & IV for company products under development. Participates in adverse event reporting and safety responsibilities monitoring. Coordinates and provides reporting information for reports submitted to the regulatory agencies. Monitors adherence to protocols and determines study completion. Coordinates and oversees investigator initiations and group studies. May participate in adverse event reporting and safety responsibilities monitoring. May act as consultant/liaison with other corporations when working under licensing agreements. Qualifications Education : MD Pharmacology (Mandatory) Experience - 2 - 5years

About Amgen Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. About The Role Role Description: The Sr Associate IS Business System Analyst position offers a unique opportunity to join a fun, innovative engineering team within the AI & Data Science (AI&D) - organization. You’ll work on next-generation capabilities and services in Applied AI & Automation using innovative COTS products, open-source software, frameworks, tools, and cloud computing services. The role also emphasizes demonstrating these capabilities to support critical business operations and initiatives, in ensuring quality, compliance, and performance across Amgen’s Applied AI & Automation Footprint. The role leverages domain and business process expertise to detail product requirements as epics and user stories, along with supporting artifacts like business process maps, use cases, and test plans for the software development teams. This role involves working closely with developers and business analysts to ensure that the technical requirements for upcoming development are thoroughly elaborated. This enables the delivery team to estimate, plan, and commit to delivery with high confidence and identify test cases and scenarios to ensure the quality and performance of IT Systems. You will collaborate with Product Managers and developers to maintain an efficient and consistent process, ensuring quality deliverables from the team. Roles & Responsibilities: Collaborate with System Architects and Product Managers to manage business analysis activities, ensuring alignment with engineering and product goals Capture the voice of the customer to define business processes and product needs Work with Product Managers and customers to define scope and value for new developments Collaborate with Engineering and Product Management to prioritize release scopes and refine the Product backlog Ensure non-functional requirements are included and prioritized in the Product and Release Backlogs Facilitate the breakdown of Epics into Features and Sprint-Sized User Stories and participate in backlog reviews with the development team Clearly express features in User Stories/requirements so all team members and stakeholders understand how they fit into the product backlog Ensure Acceptance Criteria and Definition of Done are well-defined Work closely with UX to align technical requirements, scenarios, and business process maps with User Experience designs Stay focused on software development to ensure it meets requirements, providing proactive feedback to stakeholders Develop and execute effective product demonstrations for internal and external stakeholders Maintain accurate documentation of configurations, processes, and changes Identify inefficiencies and bottlenecks Recommend data-driven solutions for process optimization Basic Qualifications and Experience: Master's degree / Bachelor's degree and 5 to 9 years in Life Science/Biotechnology/Pharmacology/Information Systems experience Functional Skills: Must-Have Skills : Excellent problem-solving skills and a passion for tackling complex challenges in drug discovery with technology Excellent communication skills and the ability to interface with business leadership with confidence and clarity Experience in writing requirements for development of modern web application and/or automation solutions Has experience with writing user requirements and acceptance criteria in agile project management systems such as JIRA Experience with business process design / re-engineering Good-to-Have Skills: Experience with tools like SIPOC diagrams, value stream maps, and process capability analysis Experience with Agile software development methodologies (Scrum) Experience with BMPN modeling tools Familiarity with GxP, CFR 21 Part 11 and systems validation Familiarity with Automation technologies (e.g., UiPath, Docusign, Power Platform, Chat GPT, etc.) Demonstrated expertise in a scientific domain area and related technology needs Understanding of scientific software systems strategy, governance, and infrastructure Experience in managing product features for PI planning and developing product roadmaps and user journeys Familiarity with low-code, no-code test automation software Technical thought leadership Able to communicate technical or complex subject matters in business terms Jira Align experience Knowledge of network security protocols and tools (e.g., IPSEC, SSL, IDS/IPS, firewalls) Experience of DevOps, Continuous Integration, and Continuous Delivery methodology Professional Certifications SAFe for Teams certification (Optional but valuable) Lean Six Sigma certification (Optional but valuable) BABOK (BA Body of Knowledge) certifications (e.g., ECBA, CCBA, CBAP) (Optional but valuable) Soft Skills: Able to work under minimal supervision Skilled in providing oversight and mentoring team members. Demonstrated ability in effectively delegating work Excellent analytical and gap/fit assessment skills Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation Ability to manage multiple priorities successfully Team-oriented, with a focus on achieving team goals Strong presentation and public speaking skills EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with 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 an accommodation.

Specific Need: Ph.D in Pharmaceutics, M Pharm in Ceuitics, Analysis, Microbiology, Pharmacognosy. Supervise B Pharm and MPharm students in research projects and dissertations. Conduct student assessments, exams, and provide academic counseling.

Diagnose and treat cancer patients, providing personalized treatment plans including chemotherapy, radiation, and immunotherapy. Conduct research and stay updated on the latest advancements in oncology treatments. Collaborate with a team of surgeons, radiologists, and pathologists to ensure comprehensive patient care. Must have an MD/MS/M.Ch degree with extensive experience in medical oncology. Experience in clinical trials and cancer research publications is a plus. Mandatory Key Skills medical oncology,clinical trials,cancer research,chemotherapy,clinical research,patient care,Oncology*

Role & responsibilities An Assistant Professor in Pharmacology is a faculty position at a university or research institution, focusing on the study of drugs and their effects on living organisms . They teach pharmacology courses, conduct research in the field, and mentor students. Key Responsibilities: Teaching: Delivering lectures, conducting lab sessions, and assessing students' understanding of pharmacological principles. Research: Conducting experiments, analyzing data, publishing findings in scientific journals, and seeking research funding. Mentoring: Advising and guiding graduate and undergraduate students on their academic and research pursuits. Service: Contributing to departmental activities, such as curriculum development and outreach programs. Qualifications: Ph.D. in Pharmacology or a related field: This is the standard requirement for an Assistant Professor position. Strong research background: A Ph.D. thesis, publications in peer-reviewed journals, and research experience are essential. Teaching experience: Experience in teaching or presenting research findings is also valuable. Communication and interpersonal skills: Effective communication and mentorship abilities are crucial for interacting with students and colleagues. Analytical and research skills. Laboratory techniques. Scientific knowledge. Communication skills. Teamwork. Attention to detail. MBBS, MD, Ph.D in Pharmacology Qualification. Preferred candidate profile

Medcare Hospitals Medical Centres is looking for Pharmacist to join our dynamic team and embark on a rewarding career journey Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including verifying order entries, maintaining records of controlled substances, charges, and removing expired and/or damaged drugs from the pharmacys inventory. Adhering to applicable legal rules, regulations, and procedures governing pharmaceutical practice. Performing other administrative tasks when needed. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before

Medcare Hospitals Medical Centres is looking for Pharmacist to join our dynamic team and embark on a rewarding career journey Dispensing Medications: Review prescriptions from healthcare providers to verify their accuracy and appropriateness Dispense medications to patients, ensuring the correct dosage and instructions are provided Patient Counseling: Offer counseling to patients on how to take their medications properly, including dosage instructions, potential side effects, and any precautions they should be aware of Medication Review: Perform medication reviews to identify potential drug interactions, allergies, or other issues that could impact a patient's health or treatment plan Medication Management: Collaborate with healthcare providers and patients to develop personalized medication management plans for chronic conditions or complex drug therapies Drug Information: Stay updated with the latest drug information, including new medications, dosage forms, and potential drug interactions Provide evidence-based information to other healthcare professionals and patients Pharmacy Operations: Oversee pharmacy operations, ensuring the accurate and timely dispensing of medications, proper inventory management, and compliance with regulatory requirements Compounding Medications: In some settings, pharmacists may be involved in preparing customized medications, especially in hospital or specialty pharmacy settings Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before

Medcare Hospitals Medical Centres is looking for Senior Pharmacist to join our dynamic team and embark on a rewarding career journey Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including verifying order entries, maintaining records of controlled substances, charges, and removing expired and/or damaged drugs from the pharmacys inventory. Adhering to applicable legal rules, regulations, and procedures governing pharmaceutical practice. Performing other administrative tasks when needed. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before

JOB SUMMARY : We are looking for a compassionate and skilled Staff Nurse to provide high-quality nursing care to patients across all departments. The ideal candidate will be responsible for assessing patient needs, planning and implementing nursing care, administering medications, and collaborating with doctors and healthcare teams to ensure the best possible patient outcomes. A staff nurse must demonstrate empathy, clinical competence, and adherence to hospital policies and nursing standards. DUTIES & RESPONSIBILITIES :  Provide bedside nursing care to patients, including monitoring vital signs, administering medications, and assisting in procedures.  Carry out doctors’ orders accurately and promptly.  Maintain proper patient records, nursing notes, and documentation in accordance with hospital protocols.  Assist in admission, transfer, and discharge of patients.  Prepare and maintain patient care areas, ensuring cleanliness and infection control standards.  Educate patients and their families about health conditions, medications, and post-discharge care.  Observe and report changes in patient condition to doctors and senior nurses.  Assist in emergency management, including CPR, first aid, and code blue situations. Coordinate with other departments (lab, radiology, pharmacy) for smooth patient care services.  Ensure safe handling and proper inventory of medicines, equipment, and supplies.  Follow biomedical waste management protocols and maintain aseptic techniques.  Participate in ward meetings, training sessions, and hospital quality improvement initiatives. EDUCATION QUALIFICATION : GNM/B.Sc. Nursing with registration under State Nursing Council KNOWLEDGE EXPERIENCE : 2YEARS MANDATORY SKILLS :  Strong knowledge of nursing procedures, clinical protocols, and patient care standards.  Familiarity with pharmacology, medication administration, and dosage calculations.  Understanding of infection control practices, biomedical waste disposal, and patient safety standards.  Proficiency in handling medical equipment (BP apparatus, infusion pumps, monitors, oxygen delivery systems).  Ability to identify early warning signs of patient deterioration and escalate appropriately.  Good communication and interpersonal skills for effective patient and family counseling.  Ability to work in rotational shifts, including nights, weekends, and emergencies.  Emotional resilience, empathy, and ability to work in stressful situations.  Teamwork and collaboration skills for working with doctors, nurses, and allied healthcare staff.  Basic computer skills for electronic medical records (EMR) documentation. Job Type: Full-time Pay: ₹20,000.00 - ₹350,000.00 per month Work Location: In person

Key Responsibilities : Reading and understanding research papers from leading pharmacology journals. Extracting key data things like drug names, mechanisms of action, side effects, and pharmacokinetic details. Categorizing this data using a user-friendly tool, ensuring its structured and ready for use by the people who need it. Skills and Competencies : Capable of understanding patents/articles related to different areas of chemistry (main focus: Pharmacology). Ability to deal with the excerption / extraction of pharmacological data from articles and patents. Serves as an educational resource to the team to assist with pharmacological assays. Participates and plans activities as needed to maintain an awareness of the current and emerging quality issues of the organization. Has an ability to explain and discuss why and how the error occurred during feedback and training discussions Able to analyze an error and identify preventive measures Has a high-level technical knowledge to edit according to specifications and main controlling areas Ability to face quality issues with customer, internal and/or external, write and convey appropriately and independently, in order to improve and promote project. Regards, Manvi Rana

About the job Sage Publishing is looking for Scientific Editors to join our STM Open Access journals team, which includes the titles Journal of International Medical Research and Science Progress . The Scientific Editors will work on medical manuscripts and perform initial scope checks and decision making on assigned journals, making best use of their in-depth understanding of topics and publishing in accordance with Sage policies and publishing standards. They will also provide expert input in areas of editorial board recruitment, special projects, journal development/strategy and optimising workflows and processes. The person needs to be a team player and uphold diversity, equity, and inclusion (DEI) principles in their daily work. Key Accountabilities Assess submitted papers on a broad range of topics within the aims and scopes of assigned journals Make 'final accept' decisions on manuscripts at a level of deep understanding of the subject matter, involving interrogating peer reviewers' comments and author's responses Keep up to date with latest relevant research and publishing practices to be confident in making final decisions across the full scope of their journals Using your expertise, provide input into Editorial Board recruitment, suggest potential Special Collection topics and Guest Editors for our Commissioning team and provide insight for our marketing initiatives Collaborate with internal and external stakeholders, in particular the Senior Scientific Editor, Journal Manager and Editorial Board members to ensure journal quality and reputation Manage a high volume of submissions annually, ensuring journal performance metrics and KPIs are achieved, and that high-quality publishing is maintained Work within an inclusive and collaborative environment, promoting diversity, equity, and inclusion (DEI) for team members and academic contributors, advocate for DEI principles in manuscript evaluation. Skills, Qualifications & Experience A PhD in a medical science such as pharmacology or biochemistry Previous editorial experience in scholarly publishing and/or postdoctorate experience would be of benefit Ability to review and evaluate research and learn new areas of research Develop expertise in a broad range of topics within the scope of assigned journals Strong analytical and decision-making abilities, and a keen eye for detail to ensure consistent quality of work Excellent communication skills and ability to work collaboratively in an international setting Ability to efficiently manage and prioritize a high volume of manuscript submissions through to final decision Commitment to research integrity, transparency, and open science A proactive, growth-focused mindset, good commercial awareness and a strong understanding of the Open Access journals publishing business and processes. Join us and be part of a mission-driven, independent publisher. You’ll work with a diverse group of people who share a passion for empowering researchers, educators, and institutions to shape the future. About Sage Sage is a global academic publisher of books, journals, and library resources with a growing range of technologies to enable discovery, access, and engagement. Believing that research and education are critical in shaping society, Sara Miller McCune founded Sage in 1965. Today, we are controlled by a group of trustees charged with maintaining our independence and mission indefinitely. Our Guaranteed Independence Means We’re Free To Do more – supporting an equitable academic future, furthering disciplines that drive social change, and helping social and behavioural science make an impact Work together – building lasting relationships, championing diverse perspectives, and co-creating resources to transform teaching and learning Think long-term – experimenting, taking risks, and investing in new ideas. A cover letter is important to us but is not essential for your application. It offers the hiring manager valuable insights into how your skill set aligns with the role, what unique contributions you can bring to the team and why you are interested in this position. Diversity, Equity, and Inclusion Sage is committed to Diversity and Inclusion and is an equal opportunities employer. We value individuality and therefore welcome all qualified applications from a diverse range of candidates.

Position: Anesthesia Technician Department: Anesthesiology Location: Santiniketan Medical College & Hospital, Santiniketan, West Bengal Job Type: Full-Time Santiniketan Medical College & Hospital is seeking a skilled and dedicated Anesthesia Technician to join our dynamic surgical team. The ideal candidate will be a crucial member of the anesthesiology department, ensuring that all anesthesia equipment and supplies are prepared and maintained to the highest standards for patient safety and care. Job Summary The Anesthesia Technician provides essential support to the Anesthesiologist and the entire surgical team before, during, and after medical procedures. This role involves preparing, operating, and maintaining anesthesia equipment, as well as stocking necessary supplies and medications. Your work will directly contribute to the safe and effective administration of anesthesia to our patients. ## Key Responsibilities Equipment Preparation and Maintenance: Set up, calibrate, and test anesthesia machines, monitors, and other related equipment before each surgical case. Perform routine cleaning, sterilization, and maintenance of all anesthesia equipment according to hospital protocols and manufacturer guidelines. Troubleshoot equipment malfunctions and perform minor repairs or escalate issues to the biomedical engineering department as needed. Ensure all equipment, such as laryngoscopes, intubation tubes, and breathing circuits, are in perfect working order. Clinical Support: Assist the Anesthesiologist with patient preparation, including positioning, monitoring, and intravenous (IV) line setup. Anticipate the Anesthesiologist's needs during procedures and promptly provide required instruments, supplies, and medications. Assist with the insertion of invasive monitoring lines (e.g., arterial lines, central venous catheters) under the direct supervision of the Anesthesiologist. Operate specialized equipment such as blood gas analyzers and cell savers as directed. Inventory and Supply Management: Maintain adequate stock levels of all anesthesia supplies, medications, and disposable items in operating rooms, carts, and storage areas. Order and receive new supplies, ensuring proper storage and rotation of stock to prevent expiry. Prepare and organize anesthesia carts and workstations for scheduled procedures. Safety and Compliance: Adhere strictly to all hospital policies, infection control protocols, and safety standards. Ensure a clean and safe work environment in the operating theatre and related areas. Participate in departmental quality assurance and improvement initiatives. ## Qualifications and Skills Education: A Diploma or Bachelor's Degree (B.Sc.) in Anesthesia Technology or Operation Theatre Technology from a recognized institution is required. Experience: A minimum of 1-2 years of experience working as an Anesthesia Technician in a hospital or surgical setting is highly preferred. Freshers with exceptional skills and knowledge may be considered. Certifications: Certification in Basic Life Support (BLS) and Advanced Cardiac Life Support (ACLS) is a plus. Technical Skills: In-depth knowledge of anesthesia machines, monitoring devices, and surgical equipment. Licensed by Google Proficiency in setting up and troubleshooting anesthesia equipment. *Familiarity with medical terminology and pharmacology related to anesthesia. Personal Attributes: Excellent attention to detail and organizational skills. Ability to remain calm and work efficiently in high-pressure situations. Strong communication and interpersonal skills to collaborate effectively with the surgical team. A compassionate and patient-centric approach. Job Type: Full-time Pay: ₹164,614.19 - ₹418,531.33 per year Work Location: In person

SENIOR RESIDENT IN PHARMACOLOGY JOB IN TRICHY, TAMILNADU, INDIA Designation: SENIOR RESIDENT IN PHARMACOLOGY Qualification: MD PHARMACOLOGY Required Experience: As per NMC norms Male or Female doctors Tamil speaking doctors preferred

SENIOR RESIDENT IN PHARMACOLOGY JOB IN TRICHY, TAMILNADU, INDIA Designation: SENIOR RESIDENT IN PHARMACOLOGY Qualification: MD PHARMACOLOGY Required Experience: As per NMC norms Male or Female doctors Tamil speaking doctors preferred

Job Title Project Manager (Clinical Studies) Business Unit Clinical Research Location: Mumbai At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key Responsibilities Lead a team of clinical research professionals and collaborate with cross-functional stakeholders. Develop and implement project plans, including timelines, milestones, and resource allocation. Define project objectives, deliverables, and success criteria in collaboration with stakeholders. Identify risks and develop mitigation strategies to ensure project success. Allocate resources, assign tasks, and monitor team performance to ensure project goals are met. Develop project budgets, track expenses, and ensure cost-effective utilization of resources. Collaborate with finance and procurement teams to manage contracts, vendor selection, and outsourcing activities. Monitor project progress and resource allocation to ensure efficient utilization and adherence to budgetary guidelines. Ensure adherence to applicable regulatory guidelines, Good Clinical Practice (GCP), and other relevant standards. Oversee the preparation and submission of regulatory documents to ethics committees and regulatory authorities. Implement quality control measures to ensure data integrity, accuracy, and compliance throughout the project Job Requirements Educational Qualification Bachelor's or Master's degree in a field related to Science, Healthcare, Clinical Research or Life Sciences like Biology, Pharmacology, Nursing, or a related discipline, and/or Post-graduate Diploma in Clinical Research. Experience Relevant experience of 5-10 years minimum in the field of Clinical Research. Additional Skills Knowledge on GCP practices, regulatory guidelines in Clinical Trials Phase III and Phase IV Clinical Trials knowledge expertise Site Management expertise Collaboration with cross functional stakeholders Team Management and creating high performing teams Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Education: * B.Pharmacy/M.Pharmacy/Pharma-D * BSC/MSC in Nursing * BPT / BHMS / BAMS * Candidates should be 2024/2023/2022 passed outs *Should have 60% (CGPA 6.5) and above throughout the academics Other Skills: * Should possess good clinical knowledge and have wide awareness around anatomy, pharmacology and disease process * Good analytical and problem-solving skills * Ability to work independently and be flexible to work in shifts (WFO) * Good verbal and written communication