1075 Pharmacology Jobs - Page 4

Urgent Requirement of Associate Professor Pharmacology Positions- Senior resident/ Assistant Professor/ Associate Professor/ Professor Qualification- MD Pharmacology Salary- Best in industry Accommodation- based on availability Job Type: Full-time Schedule: Day shift Work Location: In person

Job description Required Candidate profile We are currently looking to hire For Medical Faculty for a Reputed medical college in Jabalpur(MP), College is NMC approved and recognized. Job Role:- Assistant Professor Profile also available:-Senior Resident, Associate Professor- PHARMACOLOGY Qualification:- MBBS, MD Eligibility Criteria:- As per NMC norms Experience teaching and mentoring students at the undergraduate and graduate level Salary:- Salary As Per industrial Norms. Salary-Also Negotiable-Depends on Academic knowledge/ exposure. Job Types: Full-time, Permanent Responsibilities: Teach undergraduate and graduate-level courses in pharmacology Mentor students in research projects and independent studies Conduct independent research in the field of pharmacology and publish findings in peer-reviewed journals Participate in departmental and college-wide committees Contribute to the development and implementation of departmental and college-wide initiatives Represent the college and department at national and international conferences. Note:- Joining:- on immediate basis. Mail Id-deepti.j@ssmch.in, hr@ssmch.in, shalini.ssmch.in@gmail.com Contact-8982739001,9131379699,9425325688 Job Types: Full-time, Permanent Pay: Up to ₹1,800,000.00 per year Experience: total work: 1 year (Preferred) Work Location: In person

Key Responsibilities: Transcription: Converting voice recordings of medical professionals (doctors, nurses, etc.) into written documents, such as patient histories, discharge summaries, and operative reports. Review and Editing: Reviewing and editing medical documents created using speech recognition software, ensuring accuracy and clarity. Medical Terminology Expertise: Demonstrating a strong understanding of medical terminology, anatomy, and pharmacology to accurately interpret and transcribe medical information. Formatting and Proofreading: Ensuring that transcriptions are formatted according to industry standards and proofreading for grammar, punctuation, and spelling errors. Record Management: Managing and organizing medical records, potentially involving electronic health record (EHR) systems. Compliance: Adhering to confidentiality regulations, such as HIPAA, and maintaining patient privacy. Collaboration: Potentially interacting with healthcare providers to clarify information and ensure accurate documentation. Required Skills: Listening Skills: Excellent auditory skills to accurately understand and interpret dictation. Typing Skills: Proficiency in typing with speed and accuracy. Medical Terminology Knowledge: A strong foundation in medical language and terminology. Attention to Detail: Meticulous attention to detail to ensure accuracy in medical records. Computer Skills: Familiarity with transcription equipment, software, and EHR systems. Communication Skills: Ability to communicate effectively with healthcare providers and other team members. Time Management: Ability to prioritize tasks and manage workload effectively. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹25,000.00 per month Benefits: Leave encashment Paid sick time Paid time off Provident Fund Experience: Medical transcription: 2 years (Preferred) Work Location: In person

Role & responsibilities Dispense medications to patients according to prescriptions and provide guidance on usage. Maintain accurate records of patient interactions, including medication dispensed and dosage instructions. Monitor inventory levels of pharmaceuticals and manage stock accordingly. Provide counseling to patients about their medications, including potential side effects and interactions with other drugs. Ensure compliance with regulatory requirements for handling controlled substances Preferred candidate profile D/B/M PHARMACY SSC - ANY DEGREE WITH RETAIL PHARMACY EXPERIENCE

Job Description Field Manager, Technical This role is responsible for providing technical support to the concerned Zonal Sales team, by conducting technical training related to animal health and products to AFMs, organizing and participating in the technical seminars/ meetings for Animal Health practitioners and dairy Farmers in coordination with the Sales team for sharing technical information and attending customer complaints. Primary Responsibilities Include, But Are Not Limited To Providing Technical Services to internal team and external customers in assigned geography including on-site customer visits & off-side telephonic support as well. Executing a comprehensive technical service plan for maximizing Organizational goals. Group customer meetings to create awareness about relevant scientific practices and advancements with the objective of becoming a partner of choice among customers. Technical upgradation of the internal sales team in assigned geography Staying ahead of the curve for recent technical developments in the Ruminant Industry and preparing internal competencies to provide customer support. Supervising local clinical trials and market support studies under the guidance of the national technical manager. Supervise and provide timely and effective technical materials that maximize selling efforts. Techno-commercial view while discussing with customers. Collaboration with relevant Technical & Veterinary Education institutes in assigned geographies to further improve our image as Science Driven Organization Any other assigned task which can help in improving business. Qualifications Degree in Veterinary Sciences B.V.Sc. & A.H. (M.V.Sc. will be preferred) 2-3 years of field experience to handle all field situations and provide technical solutions to customer needs. Skills & Competencies English communication, technical training and presentation, Knowledge of animal health & diseases, Veterinary Gynecology, Medicine, Pharmacology, Animal Health Management, and Pharma product experience is highly essential. An individual has the confidence to handle adverse situations in the field.Role Specific To provide technical support to the sales and marketing team and meet their training needs and handle customer technical complaints. opportunity employer, committed to fostering an inclusive and diverse workplace. 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 Domestic VISA Sponsorship Travel Requirements 75% Flexible Work Arrangements Not Applicable Shift Valid Driving License Hazardous Material(s) Required Skills Preferred Skills Accountability, Accountability, Animal Biotechnology, Animal Health Care, Animal Husbandry, Animal Physiology, Animal Science, Client Facing, Client Management, Clinical Trial Designs, Clinical Trials, Collaboration Tools, Communication, Competency Mapping, Cow Milking, Customer Engagement, Customer Marketing, Customer Satisfaction, Customer Service, Customer Service Management, Dairy Science, Document Management, Field Auditing, Field Marketing, Field Research {+ 23 more} Job Posting End Date 07/31/2025 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 R293230

As an Assistant Professor/Professor in a Pharmacy college located in Poonamallee, Chennai, you will be responsible for delivering high-quality education in the field of Pharmacy. If you are interested in this opportunity, please forward your profile to hrasst2@ssiet.in. The ideal candidate for this position should possess an M.Pharm with Ph.D/Pharm.D qualification. For the role of Pharm.D, a minimum of 3 years of experience is required. As an Assistant Professor in Pharmacognosy/Pharmaceutics, you should have at least 3 years of experience. For the position of Professor in Pharmaceutics, Pharmacology, or Pharmaceutical Chemistry, a minimum of 10 years of experience is preferred. This is a permanent position with a day shift schedule. Immediate joiners are preferred. The educational requirement for this position is a Master's degree, and candidates with relevant work experience of 3 years are preferred. If you are interested in joining our team and meet the qualifications mentioned above, we encourage you to apply. Thank you for considering this opportunity.,

As a Manager Coding specializing in Outpatient Coding within the Quality department, you are expected to have a minimum of 8 years of experience in the Medical Coding industry. Your expertise should encompass Inpatient coding, Medical Coding guidelines, and Coding Techniques such as ICD-10 and CPT. It is essential to possess a strong knowledge of Anatomy & Physiology, Advanced Medical Terminology, Psychology, and Pharmacology. Proficiency in using MS Office tools is required along with exceptional communication and interpersonal skills. Your primary responsibilities will involve supervising and managing a team of over 50 Quality Analysts. You are tasked with fostering a motivating team environment that promotes open communication. Capacity planning for the Quality Assurance team based on project requirements, task delegation, setting deadlines, and ensuring quality control in line with client Service Level Agreements (SLAs) are key aspects of your role. Furthermore, it is your duty to oversee the effective implementation of the organization's Quality Management System, monitor team performance metrics, conduct random audits, and perform Root Cause Analysis (RCA) on audit observations. Identifying knowledge gaps and collaborating with quality leads and operation managers to develop improvement action plans is crucial. Discovering training needs, offering coaching to Quality Analysts, resolving conflicts, recognizing achievements, promoting creativity, suggesting team-building activities, and initiating improvement plans are additional responsibilities. To excel in this role, you must possess a minimum of 8 years of experience in Medical Coding, either in Operations or Quality teams specializing in IP DRG or Outpatient medical Coding. Leadership experience managing medium to large teams, particularly across multiple sites, is essential. Holding certifications such as CPC, CIC, COC, or CSS would be advantageous. A successful candidate for this role should hold a Graduate or Post Graduate degree in any field, demonstrating a strong foundation for effective leadership and management within the Medical Coding domain.,

The Assistant Manager Proposal Management (Translational & Clinical Research) role at Syngene International Ltd. in Bangalore, within the Commercial department, involves contributing to the creation and delivery of high-quality proposals within the Clinical Development Business Unit. Syngene, an innovation-focused organization, provides integrated scientific services to various industries globally, with a clientele including renowned companies such as Bristol-Myers Squibb, Baxter, and GSK. Key responsibilities of the role include taking complete responsibility for proposal quality, ensuring timely delivery to the business development team, collaborating with technical and business development teams for competitive pricing, and liaising with vendors for necessary information. The role also involves updating deal trackers, coordinating contractual agreements, and transitioning awarded deals to the project management team. Educational qualifications required for the position include an M.Tech/Master's degree in Clinical Research/Pharmacology/Biotechnology or Life Sciences, with an MBA being desirable. Technical skills should include knowledge and experience in Translational & Clinical Research services, proficiency in Microsoft Office applications, strong planning and multitasking abilities, excellent communication skills, and familiarity with pre-sales/proposal management functions. Candidates should possess 8-10 years of experience in Contract Research Organization/Clinical research, with prior experience in Presales/Proposal Management being advantageous. Behavioral skills required for the role include attention to detail, team management capabilities, and proactive teamwork. The successful candidate will also be responsible for adhering to environment, health, and safety (EHS) requirements and ensuring their team's compliance with EHS measures. Syngene International Ltd. is an Equal Opportunity Employer committed to providing a supportive and inclusive work environment for all employees.,

Job Title: Branch Name: Brain and Spine Medicity Qualification: B. Pharm Location: Kannur Employment Type: Full time Department: Neuro rehabilitation \u200b 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. \u200b 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 ","

We are Reckitt Home to the worlds best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Research & Development In Research and Development, were full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality. The size of our organisation means youll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation. About the role As a Regulatory Assistant, you ll be at the forefront of our innovation and compliance efforts. You ll jumpstart your career in a role that provides a blend of strategic thinking and hands-on experience within a dynamic, collaborative environment. If you have a passion for science and a drive to ensure the safety and efficacy of consumer products, your skills could be a perfect match for us. Together, we will work to navigate the exciting regulatory landscape, ensuring our diverse product range not only meets but exceeds the highest standards. Your responsibilities - Support the development and rollout of new products by navigating regulatory requirements and maintaining compliance. - Engage with regulatory authorities, staying abreast of the changing landscape and expertly managing product compliance. - Contribute to the team by formatting and compiling regulatory submission documents under guidance. - Access and understand regulations and guidelines, applying them effectively to projects, as directed. - Communicate and interact with cross-functional teams, playing a pivotal role in project meetings to understand objectives. The experience were looking for - 0-3 years of experience within the regulatory field, ideally supported by a BSc or MSc in a scientific discipline such as chemistry, biomedicine, or pharmacology. - Ability to work under pressure while ensuring task execution and adherence to deadlines. - Developing business acumen and commercial awareness, with a view to understanding product lifecycle management. - Capacity for insight into consumer needs and expectations. - Eagerness to collaborate, build partnerships, and continuously innovate. The skills for success Task Execution Under Pressure, Business Acumen, Commercial Awareness, Objective Setting, Accountability, Consumer Insight, R&D, Product Lifecycle Management, Intellectual Property, Business Partnership, Collaboration and partnership building, Adapt to changes in technological development plans, Ability to challenge the status quo and propose improvement, Innovation Processes. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way.We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitts potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitts pay for performance philosophy. We recognise that in real life, great people dont always tick all the boxes. Thats why we hire for potential as well as experience. Even if you dont meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you.All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.

We are Reckitt Home to the worlds best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Research & Development In Research and Development, were full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality. The size of our organisation means youll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation. About the role As a Regulatory Assistant, you ll be at the forefront of our innovation and compliance efforts. You ll jumpstart your career in a role that provides a blend of strategic thinking and hands-on experience within a dynamic, collaborative environment. If you have a passion for science and a drive to ensure the safety and efficacy of consumer products, your skills could be a perfect match for us. Together, we will work to navigate the exciting regulatory landscape, ensuring our diverse product range not only meets but exceeds the highest standards. Your responsibilities - Support the development and rollout of new products by navigating regulatory requirements and maintaining compliance. - Engage with regulatory authorities, staying abreast of the changing landscape and expertly managing product compliance. - Contribute to the team by formatting and compiling regulatory submission documents under guidance. - Access and understand regulations and guidelines, applying them effectively to projects, as directed. - Communicate and interact with cross-functional teams, playing a pivotal role in project meetings to understand objectives. The experience were looking for - 0-3 years of experience within the regulatory field, ideally supported by a BSc or MSc in a scientific discipline such as chemistry, biomedicine, or pharmacology. - Ability to work under pressure while ensuring task execution and adherence to deadlines. - Developing business acumen and commercial awareness, with a view to understanding product lifecycle management. - Capacity for insight into consumer needs and expectations. - Eagerness to collaborate, build partnerships, and continuously innovate. The skills for success Task Execution Under Pressure, Business Acumen, Commercial Awareness, Objective Setting, Accountability, Consumer Insight, R&D, Product Lifecycle Management, Intellectual Property, Business Partnership, Collaboration and partnership building, Adapt to changes in technological development plans, Ability to challenge the status quo and propose improvement, Innovation Processes. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way.We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitts potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitts pay for performance philosophy. We recognise that in real life, great people dont always tick all the boxes. Thats why we hire for potential as well as experience. Even if you dont meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you.All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.

Job Title : Pharmacovigilance Specialist Location : Bangalore / Hyderabad Experience : Minimum 4 Years in PV ICSR Job Summary We are seeking a skilled and detail-oriented Pharmacovigilance (PV) Specialist with hands-on experience in Individual Case Safety Reports (ICSR) . The ideal candidate will be responsible for end-to-end case processing and ensuring compliance with global PV regulations and internal SOPs. Key Responsibilities : Perform case intake, triage, data entry, quality review, and submission of ICSRs. Evaluate and code adverse event reports using MedDRA and WHO-DD coding. Ensure timely reporting of adverse events to regulatory authorities and clients. Maintain compliance with pharmacovigilance regulations (e.g., FDA, EMA, CDSCO). Collaborate with cross-functional teams to ensure accurate and complete safety data. Contribute to audit and inspection readiness. Prepare periodic safety update reports (PSURs) and other regulatory documents when required. Qualifications : Bachelors or Masters degree in Pharmacy, Life Sciences, or related field. Minimum 4 years of hands-on experience in PV ICSR processing. Strong understanding of global PV regulations and ICH-GCP guidelines. Familiarity with PV databases (e.g., Argus, ArisG) is an advantage. Excellent attention to detail and strong analytical skills. Good communication and documentation skills. Preferred Attributes : Certification in Pharmacovigilance will be an added advantage. Ability to work independently and as part of a team. Willingness to work in shifts if required (based on client/region).

Job Title : Pharmacovigilance Specialist Location : Bangalore / Hyderabad Experience : Minimum 2 Years in PV ICSR Job Summary We are seeking a skilled and detail-oriented Pharmacovigilance (PV) Specialist with hands-on experience in Individual Case Safety Reports (ICSR) . The ideal candidate will be responsible for end-to-end case processing and ensuring compliance with global PV regulations and internal SOPs. Key Responsibilities : Perform case intake, triage, data entry, quality review, and submission of ICSRs. Evaluate and code adverse event reports using MedDRA and WHO-DD coding. Ensure timely reporting of adverse events to regulatory authorities and clients. Maintain compliance with pharmacovigilance regulations (e.g., FDA, EMA, CDSCO). Collaborate with cross-functional teams to ensure accurate and complete safety data. Contribute to audit and inspection readiness. Prepare periodic safety update reports (PSURs) and other regulatory documents when required. Qualifications : Bachelors or Masters degree in Pharmacy, Life Sciences, or related field. Minimum 2 years of hands-on experience in PV ICSR processing. Strong understanding of global PV regulations and ICH-GCP guidelines. Familiarity with PV databases (e.g., Argus, ArisG) is an advantage. Excellent attention to detail and strong analytical skills. Good communication and documentation skills. Preferred Attributes : Certification in Pharmacovigilance will be an added advantage. Ability to work independently and as part of a team. Willingness to work in shifts if required (based on client/region).

Kamineni academy of medical sciences is looking for Assistant Professor - Anatomy to join our dynamic team and embark on a rewarding career journey Teach a range of courses in the department, at both the undergraduate and graduate levels Conduct original research in the field and publish findings in academic journals and at conferences Advise students and mentor junior faculty members Participate in department and university-wide committees, such as curriculum committees and search committees Pursue external funding opportunities to support research and teaching activities Engage in professional development activities to stay current in the field and enhance teaching skills

Kamineni academy of medical sciences is looking for Associate Professor - Anatomy to join our dynamic team and embark on a rewarding career journey Teaching and Instruction: Associate Professors are responsible for teaching undergraduate and/or graduate-level courses in their area of expertise They develop syllabi, prepare course materials, deliver lectures, facilitate discussions, and assess student performance They may also supervise student research projects, theses, and dissertations Research and Scholarship: Associate Professors engage in research activities, pursue scholarly publications, and contribute to the advancement of knowledge in their field They conduct research projects, secure research funding, collaborate with colleagues, and publish their findings in academic journals or present them at conferences They may also mentor and guide graduate students in their research pursuits Academic Advising: Associate Professors provide academic guidance and advising to students They assist students in selecting courses, developing academic plans, and pursuing research or career opportunities within their discipline They may also serve as thesis advisors or mentors to graduate students Service and Committee Work: Associate Professors contribute to the administrative functions of their department, college, or university through service and committee work They participate in faculty meetings, serve on academic committees, contribute to curriculum development, and provide input on various institutional matters

Job Title: Trainee Pharmacist Company Name: DM Hospital Job Description: As a Trainee Pharmacist at DM Hospital, you will be an integral part of the pharmacy team, assisting in the provision of high-quality pharmaceutical care to patients. You will work under the supervision of licensed pharmacists, gaining hands-on experience in medication management, patient counseling, and pharmacy operations. Your responsibilities will include preparing and dispensing medications, conducting medication therapy management, ensuring compliance with regulatory standards, and providing support in pharmaceutical services to enhance patient health outcomes. Key Responsibilities: - Assist in the preparation and dispensation of medications, including oral and intravenous formulations. - Conduct medication reviews and assist in monitoring patient medication therapy. - Provide accurate drug information to healthcare professionals and patients. - Participate in inventory management, including stock checks and ordering of pharmaceuticals. - Support the pharmacist in counseling patients about their medications, including dosage, side effects, and interactions. - Maintain accurate records and documentation of all pharmaceutical activities. - Collaborate with healthcare team members to ensure continuity of care for patients. - Uphold compliance with laws, regulations, and standards governing pharmacy practice. Skills and Tools Required: - Strong understanding of pharmacology, pharmacy law, and medication management. - Excellent communication and interpersonal skills for effective patient interaction. - Detail-oriented with strong organizational skills to manage multiple tasks. - Ability to work collaboratively in a team environment and assist in crisis situations. - Proficient in using pharmacy management software and electronic health record systems. - Basic knowledge of medical terminologies and drug classifications. - Ability to handle and resolve conflicts in a professional manner. - Willingness to learn and adapt to new challenges in a dynamic healthcare setting. - Strong commitment to patient safety and quality of care. Qualifications: - Bachelor’s degree in Pharmacy or currently enrolled in a Doctor of Pharmacy (Pharm.D) program. - Demonstrated interest in pursuing a career in hospital pharmacy. - Previous internship or experience in a pharmacy setting is a plus but not required. - Active registration as a pharmacy student or intern under the relevant pharmacy board (if applicable). Roles and Responsibilities About the Role: - As a Trainee Pharmacist at DM Hospital, you will gain hands-on experience in pharmaceutical care. - You will work under the supervision of licensed pharmacists to support medication management and patient safety. - The role involves assisting in dispensing medications and providing patient counseling on drug therapies. About the Team: - You will be part of a multidisciplinary healthcare team dedicated to improving patient outcomes. - The pharmacy team collaborates closely with doctors, nurses, and other healthcare professionals to ensure comprehensive care. - Team members are committed to ongoing education and professional development, fostering a supportive learning environment. You are Responsible for: - Assisting pharmacists in preparing and dispensing medications accurately. - Conducting medication reconciliation and ensuring patient records are up-to-date. - Providing information and guidance to patients regarding their medications and potential side effects. To succeed in this role – you should have the following: - A genuine interest in pharmacy practice and patient care. - Strong attention to detail and excellent communication skills. - A willingness to learn and adapt in a fast-paced healthcare setting.

Job Description: Toxicologist / Preclinical Scientist We are seeking a skilled Toxicologist / Preclinical Scientist to join our team. The ideal candidate will be accountable for conducting toxicological risk assessments and overseeing preclinical experimental research. 1. Key Responsibilities: Toxicological Risk Assessments • Derive Health-based Exposure Limits & support occupational hazard assessment (PDE/OEL) for pharmaceutical molecules in adherence to regulatory standards. • Conduct Toxicological Risk Assessments (TRA) for pharmaceuticals, excipients, intermediates, chemicals, cleaning agents, residual solvents, elemental impurities, and degradation products. • Perform Genotoxicity Hazard Assessments for impurities using published or experimental in-vitro/in-vivo data and in-silico (Q)SAR tools according to ICH M7 guidelines. • Evaluate extractable and leachable impurities using literature review and in-silico tools. • Determine Harmful Doses for children to guide selection of blister packaging. 2. Key Responsibilities: Experimental Toxicology & Preclinical Research • Develop preclinical strategies supporting differentiated product development. • Plan, outsource, oversee, and interpret in vitro and in vivo preclinical toxicology and pharmacokinetics/pharmacodynamics (PK/PD) studies for complex/differentiated products and impurity qualifications. • Plan, outsource, oversee, and interpret in vivo/ in vitro biocompatibility studies for medical devices. • Plan, outsource, oversee, and interpret in vitro immunogenicity studies for peptides and biosimilar products. • Summarize toxicological data and prepare Investigational Brochures (IBs), Investigational New Drug (IND) applications, and electronic Common Technical Document (e-CTD) for regulatory authority submissions. Qualifications and Skills • Advanced degree in Toxicology, Pharmacology, Zoology, Veterinary Medicine or related field. • Minimum 3-5 years of experience in toxicological risk assessment & experimental toxicology within the pharmaceutical, CRO or biotechnology industry. • Strong understanding of regulatory guidelines (e.g., ICH, USFDA, EMA, CFDA, DCGI) and experience with regulatory submissions. • Proven ability to manage multiple projects simultaneously and work effectively in a dynamic team environment. • Excellent communication skills with the ability to collaborate cross-functionally and interact with external partners such as CROs. • Detail-oriented with proactive planning abilities, coupled with strong analytical skills, effective timeline management, adept problem-solving capabilities, and excellent collaboration and teamwork skills. • Skilled in using computer software including Microsoft Office suite (Word, Excel, PowerPoint), SharePoint, QSAR tools, data mining software, citation tools, and other relevant applications. Operational details: • Location: Vikhroli, Mumbai. • Mode: Full time, work from office • Shifts: General shift (8 hours) • Travelling: Rare/Occasional for outdoor duties/ monitoring

Respected Sir/Mam, Hiring SR/ AP, Asso. & Professor Medicine Surgeon Emergency Medicine Anesthesia Community medicine Pharmacology Forensic Biochemistry Physiology Anatomy Radiology in Medical College Qualification: MBBS & MD Vaibhav -8423159700

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

Project role : Clinical data coder 1 (MedDRA, WHODD) Work experience : 2-5 Years Work location : Bangalore Mode of work : Office based Must Have Skills: MedDRA, WHODD, Clinical data coder, clinical coding 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 and/or Coding activities, and may provide leadership either in the role of the Lead Coder or in a specific CDM task (e.g. Data Operations Coordinator (DOC) or lead a coding related task on a mega trial). Serve independently as a Clinical Data Coder and/or Lead Coder or DOC for one or more protocols. Manage delivery of coding activities and/or stand alone coding projects through full study life-cycle (with minimal guidance). 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. Manage coding related project timelines with guidance from the DOC or Data Team Lead (DTL) or Manager. Perform Serious Adverse Event (SAE) reconciliation activities. May serve as a back-up for a Lead Coder, DOC or DTL. Perform comprehensive quality control procedures, Assist in implementing new technology. • Independently bring coding and project related solutions to the DM team. Handle audit requirements for respective studies including stand-alone coding projects as applicable. Understand and comply with core operating procedures and work instructions. Perform other duties as directed by the study team or Manager, or meet objectives as assigned Develop and maintain good communication and working relationship with the team. Educational Qualification: Pharmacy, dental, medical, nursing, life sciences or related field qualification or educational equivalent Excellent knowledge of medical terminologies, pharmacology, anatomy and physiology. In-depth knowledge of medical dictionaries used for coding (e.g., MedDRA, WHODD etc.). Understanding of the Data Management process from study start-up through to database lock.

As a Pharmacist at Brain and Spine Medicity in Kannur, your primary responsibility will be to accurately dispense prescriptions as per doctors" instructions. You will be ensuring the correct dosage, route, and duration of medication while verifying prescriptions for accuracy and potential drug interactions. Collaborating with the medical staff, including doctors and nurses, will be essential to advise on substitutions, interactions, or new drug updates. Patient counseling is a crucial aspect of this role, where you will educate patients on how to take their medications properly, explain side effects, storage requirements, and precautions. Maintaining stock of medicines and medical supplies, checking expiry dates, and ensuring proper storage conditions will be part of your inventory management duties. Regulatory compliance is paramount, and you will be responsible for ensuring adherence to drug laws and medical regulations. This includes maintaining records of controlled substances and regulated drugs while managing billing for dispensed medications and maintaining accurate logs of prescriptions and dispensed drugs. Your role will also involve quality control measures such as monitoring for counterfeit or substandard drugs to ensure that all medications meet safety and quality standards. To excel in this position, you should have in-depth knowledge of pharmacology and therapeutics, attention to detail, strong communication and counseling skills, inventory and supply chain management expertise, problem-solving and decision-making abilities, familiarity with drug regulations and compliance, basic computer skills for billing and e-prescriptions, and an ethical responsibility towards patient-centered care.,

KIRTI PHARMACEUTICALS 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.

Dear All, Greetings from Vivo Bio Tech Limited! Job Description: Business Development (BD) role** in a CRO setting Experience: 3+ Job Title:** Business Development/Executive/ Manager/Sr. Manager_ Preclinical Services Location:** Hyderabad Reports To:** Head Business Development / Executive Director Job Overview: We are seeking a proactive and results-driven **Business Development Manager** to independently drive lead generation and conversion across domestic and international markets. The ideal candidate should have strong networking skills within the **CRO industry**, and proven experience in securing business from **Pharma, Agrochemicals, Industrial Chemicals, Vaccines, Generics, and Medical Devices** clients. This role requires working knowledge of **GLP compliance**, **regulatory affairs**, **toxicology studies**, and familiarity with submission processes to global regulatory bodies. Key Responsibilities:** * Independently generate, qualify, and convert leads for preclinical research services. * Submit tailored technical and commercial quotations to potential clients. * Network extensively across Pharma, Agrochemical, Vaccine, Generic Drug, Medical Device, and Chemical industries. * Understand client requirements and align them with organizational capabilities in **GLP and non-GLP studies**. * Develop and maintain strong client relationships to drive repeat and long-term business. * Coordinate with internal scientific and operational teams to design study proposals and timelines. * Provide market intelligence and competitor analysis to support strategic planning. * Track, monitor, and support **regulatory submissions** to international authorities such as USFDA, EMA, WHO, PMDA, ANVISA, etc. * Stay updated with global guidelines relevant to **Mammalian Toxicology**, **Ecotoxicology**, and **Regulatory Submissions**. * Promote services across **small and large animal studies**, including rodent, canine, minipig, and non-human primate models. * Collaborate on proposals for government and international grants or tenders (if applicable). Key Requirements:** * Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related fields. * Minimum 2–15 years of BD experience in a CRO or related preclinical research setting. * Strong understanding of **GLP requirements** and study types. * Working knowledge of **toxicology, pharmacology, ecotoxicology**, and **regulatory pathways**. * Familiarity with **GTC (General Toxicity Category)** studies and their scope. * Excellent communication, negotiation, and relationship-building skills. * Self-motivated and target-oriented with strong business acumen. * Willingness to travel domestically and internationally as required. --- Preferred Experience: * Exposure to **OECD, ICH, USFDA, EPA, REACH, and other regulatory guidelines**. * Experience in handling **multi-national clients** and long-term contracts. Vivo Bio Tech Ltd Survey # 349/A, Pregnapur Village, Gajwel Mandal. Siddipet District, PIN 502311,Telangana, India. Regards, Chandra Kanth | HRD chandrakanth.k@virinchi.com

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols Recruit, screen, and enroll study participants while maintaining accurate documentation and records Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

Clin Infotech is offering the internship opportunity for BDS MDS Dental Graduates Should have Knowledge in Pharmacovigilance Should Have knowledge on Argus & MEDDRA Applicants Should Complete Certification in Pharmacovigilance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage