2847 Pharmacology Jobs - Page 15

Eligibility : MD ANATOMY/MD GENERAL MEDICINE/MD PAEDIATRICS,MD PHARMACOLOGY,MD RADIODIAGNOSIS,MD TRANSFUSION MEDICINE,MS GENERAL SURGERY,MD MICROBIOLOGY

We are seeking a Marketing Strategist with professional expertise in rehabilitation field to join our team. The successful candidate will be responsible for bringing in clients as well as hearing aid sales by establishing rapport with doctors, hospitals, clinics, playschools and other institutions. The candidate will act as effective interface between our clinic and outside agencies/ institutions. Also, the candidate will be responsible in identifying new business opportunities, building relationships with potential client’s/ business partners, for which career growth opportunities are assured. Candidate will play vital role in developing marketing strategies both online as well as offline m...

Job Description Pharmacy professional (Pharmacist) ensures safe dispensing of medications, evaluates prescriptions, and advises patients on proper drug usage. They maintain inventory, monitor stock levels, and handle regulatory compliance. In addition, they collaborate with healthcare teams to optimise patient therapy, manage medication records, and prevent drug interactions. Their role includes patient counselling, identifying side-effects, and promoting health-awareness through responsible pharmaceutical practices. Key Responsibilities Dispense prescribed medicines accurately and verify proper dosages. Review patient prescriptions for potential drug interactions and contraindications. Coun...

What you will do In this vital role you will be part of the Product Team responsible for completing the digital roadmap strategy, ongoing design, development, management, and optimization of Amgen Operations Electronic Lab Notebook (ELN) and Instrument Data Acquisition Platform. The ideal candidate will have an excellent grasp of the technology for Lab applications with a passion for fostering innovation and excellence in the biotechnology industry. Strong preference will be given to candidates with experience working in ELN Applications, Enterprise Application Integration, end-to-end data and process harmonization, as well as handling the seamless integration of Lab Instrument data to vario...

We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you! Responsibilities Determine plan of action for incoming calls; Collect, process, and track incoming adverse and serious adverse events; Write safety narratives; Report on various safety data; and Collaborate with internal departments and investigative clinica...

- Manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. - Conducts research to ensure these products are safe. - Ordering, tracking, and managing IP and trial materials. Required Candidate profile - Knowledge of the pharmaceutical industry, terminology, and practices. - Knowledge of FDA regulations and their practical implementation. - Strong verbal and written communication skills.

Job Summary The Head of R&D – Personal Care (Ayurvedic & Herbal) will lead the development of innovative, safe, and effective personal care formulations rooted in Ayurvedic and herbal sciences. This role combines traditional knowledge with modern scientific methodologies to deliver high-quality products that meet regulatory standards and consumer expectations. Key Responsibilities: 1. Product Research & Formulation Development Lead the end-to-end development of new Ayurvedic, herbal, and natural personal care products (e.g., skincare, haircare, hygiene, body care, etc.). Conceptualize and formulate new products based on market trends, consumer needs, and Ayurvedic principles. Develop prototy...

Company Description Rama University is a distinguished academic institution committed to fostering innovation and academic excellence. With its focus on holistic learning, the university integrates practical techniques such as industry visits, guest lectures, and case studies to prepare students for real-world challenges. Rama University is approved by AICTE and UGC, ensuring high academic standards. The university operates across two fully-equipped campuses spanning 150 acres in Delhi NCR and Kanpur, Uttar Pradesh, offering a vibrant atmosphere for education and research. Role Description The Assistant Professor: Pharmacy position is a full-time, on-site role based in Kanpur. The role invol...

Job Description ROLE SUMMARY 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 & Dairy Farmers in coordination with the Sales team for sharing technical information and attending customer complaints. Responsibilities 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...

Job Description THE OPPORTUNITY The RMA (Regional Medical advisor) will be a valued representative of our company India working in the field to interact and engage key stakeholders. Our medical affairs team objective is to provide scientific expertise across their identified regions/products/therapy areas to these valued customers. What You Will Do The RMA will have the following key responsibilities Developing and implementing medical strategies Scientific leader identification development and engagement to build regional, national or international relationships to contribute to understanding of diseases, scientific trends, practice guidelines, and treatment patterns in areas relevant to ou...

Need Fresh graduate with Strong understanding of Human anatomy and physiology, Proficiency in medical terminology and ability to learn new terms quickly. Takehome salary - 15.2 K per month (After all deduction) + Yearly Bonus Direct Walk-in - Access Healthcare Head Quaters Ambattur Timings - 8th November 2025 (10 to 3 PM ) Work Location - Ambattur Kosmo One No direct walk -in only shortlisted will be called for interview, Whatsapp - 7200516569 (No calls only whatsapp message) for details We intend to hire 300 new medical coders each month. We recommend you to either enroll in a medical coding training institute or improve your knowledge in human anatomy and physiology on your own to be prepa...

Parul Hospital - India is looking for Pharmacist to join our dynamic team and embark on a rewarding career journey Dispense prescriptions and counsel patients on medications Supervise pharmacy staff and ensure inventory control Maintain compliance with drug laws and protocols Collaborate with doctors for accurate medication usage 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

Purpose And Scope This position will assist the Clinical Trial Lead (s) and Clinical Trial Manager(s) in the day-to-day operations, set-up, execution and close-out of assigned drug trials, which may include: pre/post-POC interventional drug trials, Clinical Pharmacology normal healthy volunteer clinical trials, pre-approval access and post-marketing regulatory commitment trials (interventional and non-interventional). This position is accountable to the clinical trial team for the support of the trial execution and works collaboratively with all global cross-functional team members and vendors to ensure proper set-up of trial processes and plans to execute the protocol with operational excel...

Purpose And Scope This position will assist the Clinical Trial Lead (s) and Clinical Trial Manager(s) in the day-to-day operations, set-up, execution and close-out of assigned drug trials, which may include: pre/post-POC interventional drug trials, Clinical Pharmacology normal healthy volunteer clinical trials, pre-approval access and post-marketing regulatory commitment trials (interventional and non-interventional). This position is accountable to the clinical trial team for the support of the trial execution and works collaboratively with all global cross-functional team members and vendors to ensure proper set-up of trial processes and plans to execute the protocol with operational excel...

Urgent Walk in For M.Pharmacy fresher Completed Clinical Data Management Training only Eligible CDM Certification is Mandatory Knowledge of Clinical Data Management Plan, study phase conduct phase and Close out phase Required Candidate profile Strong knowledge of cGMP and relevant regulatory requirements: This includes understanding manufacturing processes, quality control procedures, and validation requirements.

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

Perform triage & intake of ICSR received daily in ARGUS databases Should have hands On Experience On ARGUS Safety Database Should Have hands on Experience on MEDDRA Applicants Should Complete Certification in Pharmacoviiglance 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

Walk-In Interview for Pharmacy Life Science Fresh Graduates For Medical Coding Non Certified Applicants should have good knowledge in Medical Coding Anatomy and Medical Terminology Required Candidate profile Candidates Should have good knowledge in Medical Coding ICD 10, Anatomy Medical terminology and CPT

Walk-In Interview for Pharmacy Life Sciences Biotechnology Biochem Chemistry Nursing MLT Fresh Graduates For Medical Coding Non Certified Freshers Applicants should have good knowledge in Medical Coding Anatomy and Medical Terminology Required Candidate profile Candidates Should have good knowledge in Medical Coding ICD 10, Anatomy Medical terminology and CPT Exposure to CPT-4, ICD-9, ICD-10, and HCPCS coding

Walk-In Interview for Pharmacy Life Sciences Biotechnology Biochem Chemistry Nursing MLT Fresh Graduates For Medical Coding Non Certified Freshers Applicants should have good knowledge in Medical Coding Anatomy and Medical Terminology Required Candidate profile Candidates Should have good knowledge in Medical Coding ICD 10, Anatomy Medical terminology and CPT Exposure to CPT-4, ICD-9, ICD-10, and HCPCS coding

We are currently hiring for DSA I role with a minimum of 3 to 5 years Of experience in Pharmacovigilance Perform triage & intake of ICSR received daily in ARGUS databases. Ensure data entry of ICSR in ARGUS Knowledge In Aggregate Reporting is Must Required Candidate profile Require 3 to 5 years of pharmacovigilance case processing experience. Responsible for coding events using MEDDRA Any Life Sciences(B pharm/M Pharm/ Pharm D, Life Sciences, Nursing, BDS, BPT)

Hiring Fresh Pharmacy and Life Science Nursing Graduates Medical and Para Medical For Claims Associate Freshers Only Applicants should have good knowledge in Medical Coding Anatomy and Medical Terminology. Required Candidate profile Candidates Should have good knowledge in Medical Coding ICD 10, Anatomy Medical terminology and CPT Immediate Joiners Will be Preferred

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

We are currently hiring for DSA I role with a minimum of 1 year experience in Pharmacovigilance Perform triage & intake of ICSR received daily in ARGUS databases. Ensure data entry of ICSR in ARGUS Required Candidate profile A minimum of 1 year pharmacovigilance case processing experience. Responsible for coding events using MEDDRA Any Life Sciences(B pharm/M Pharm/ Pharm D, Life Sciences, Nursing, BDS, BPT) are Eligible

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols. Should have knowledge in Clinical Data Management EDC Edit Checks SAE Reconcillation Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study