Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world’s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level: - Research Associate -1 Location : - Greater Noida Department: - Synthesis Reporting Manager: - Group Leader Key Responsibilities Synthesis, purification and characterization of novel chemical compounds. Deliver small to large quantities of by novel chemical entities for drug discovery. Work collaboratively in a team to drive chemistry projects forward. Responsible for safe conduct of reactions. Excellent knowledge in basic and advance organic chemistry. Good knowledge in functional group conversion and multiple step synthesis. Basic knowledge retrosynthetic analysis (desirable). Good expertise in handling pyrophoric reactions. Good knowledge of TLC, column purification, extraction. Excellence in analyzing NMR, IR and Mass Spectrometry data. Always adhere to safe laboratory practices. Enthusiasm to work in a dynamic research environment. Always stretch when project challenge increases. Good knowledge in computer (MS-word/Excel/Power point) and structure drawing (Chem Draw/ISIS) and recording in electronic lab notebook. Good communication and presentation skill. Good in literature search using Reaxys. Person Profile Qualification: - M.Sc in Organic Chemistry or related field/ M. Pharma. Experience:- 1-5 years of industry experiences with any leading CRO organization. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. Show more Show less

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world’s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level : - RA Location: - Greater Noida Department: - Analytical Key Responsibilities Having exposure of 1-4 years in analytical chemistry, method development and analysis of regular samples on chromatographic instruments (LC-MS). Candidate should be well acquainted with the respective instrument and software. Maintenance, cleaning, documentation and calibration of analytical instruments. Demonstrate perseverance, team co-ordination and analytical approach at the work place. Should be flexible with working hours. Provide training to new joiners. Practice safe work habits including complying with all safety health and environmental rules and regulations Person Profile Qualification: - M. Sc. (Analytical Chemistry)/ M. Pharm or related field from reputed university/institute. Experience: - 1-4 years of relevant experience for Masters. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. Show more Show less

Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world’s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level: - Research Scientist/Sr. Research Scientist (L1/L2) Location : - Greater Noida Department: - Synthesis Reporting Manager: - Group Leader Key Responsibilities Synthesis, purification, and characterization of chemistry intermediates. Ability to lead 3-8 chemists. Deliver small to large quantities of lead novel chemical entities for drug discovery. Work collaboratively in a team to drive chemistry projects forward. Responsible for safe laboratory practices. Excellent knowledge of basic and advance organic chemistry. Very good knowledge of functional group conversion and multiple step synthesis. Knowledge of retrosynthetic analysis and route-designing of project. Good team leading skills of 3-8 chemists along with own-reactions. Excellent problem solving ability. Good expertise in handling various pyrophoric reactions and trouble-shooting. Good Knowledge of chiral chemistry, diastereomer separation. Excellent trouble-shooting skills in purification and extraction. Good Knowledge of (Prep)-HPLC and analyzing NMR, IR, Mass Spectrometry data. Excellent knowledge of writing and reviewing electronic lab notebooks; and writing reports, patents and manuscripts. Expertise in literature search using Reaxys/Scifinder etc. Always adhere to safe laboratory practices. Multi-tasking i.e. good in chemical ordering and maintaining lab inventory. Enthusiasm to create a dynamic research environment. Always stretch when project challenge increases. Excellent communication and presentation skill. Attention to the details. Ability to motivate team to work. Person Profile Qualification: - Ph.D in Organic Chemistry or related field /Post Doctorate Experience: - 1-5 years of industry/post-doc experiences. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. Show more Show less

Design & execute in vivo experiments using rodent models to evaluate pharmacological properties of drug candidates, focusing on dosing, administration routes, & model selection. Conduct safety & efficacy studies (oncology, metabolic disorder, skin disorders) in disease-relevant rodent models, monitor disease progression, & assess treatment endpoints following established protocols. Conduct Pharmacokinetics (PK) study in mice and rats using different modes of administrations Conduct single and multiple day dose tolerability study Analyze in vivo data, generate reports, & contribute to regulatory submissions & publications. Collaborate with cross-functional teams (in-vitro pharmacologists, medicinal chemists, bio-analytical teams) to integrate pharmacology data into drug development strategies. Ensure adherence to ethical standards & regulatory guidelines, maintaining high animal care & welfare. Oversee vivarium management, including creating SOPs & liaising with regulatory bodies (CPCSEA) Prepare reports, presentation materials, & contribute to scientific publications & regulatory submissions. Ensure compliance with local regulations, bio-safety, & data integrity standards in animal research. Job Types: Full-time, Permanent, Fresher Pay: ₹500,000.00 - ₹700,000.00 per year Benefits: Paid sick time Provident Fund Schedule: Day shift Work Location: In person

Employment Offer In Vivo Biologist at Patanjali Research Foundation, Haridwar Patanjali Research Foundation is a fully integrated innovative research institute to conduct modern experimentation on Ayurvedic medicines for the treatment of various diseases. The Institute has a diversified research portfolio and a substantial clinical testing pipeline. With its R&D centre and headquarters in Haridwar, Patanjali also has a mega manufacturing facility, an Ayurvedic hospital and medical college, a university, and herbarium along with herbal garden. Research laboratories at Patanjali are accredited with NABL, DSIR, DBT, and have CPCSEA approved animal house along with well-defined IAEC, IBSC and IEC structures. These are probably one-of-the-kind, and literally state-of-the-art facilities to conduct research on Ayurveda. Top of the line equipments and globally trained workforce energizes the research operations, on a daily basis. The In-Vivo Biologist will be a laboratory-based role responsible for developing and executing in vivo primary screening and disease differentiation models across various therapeutic areas. The candidate will contribute significantly to the design and validation of functional in vivo protocols, including molecular, biochemical, and histopathological evaluations. The role involves independent planning and execution of in vivo pharmacology and non-clinical safety studies, with meticulous documentation and analysis of experimental data. Job Responsibilities Assist in the development of in vivo primary screening, disease and differentiations models encompassing a broad range of therapeutic areas. Draft succinct study plans subsequent to extensive literature search, from the perspective of functional in vivo, biochemical, molecular and histopathological parameters. Conduct in vivo efficacy and non-clinical safety studies. Formulate exhaustive reports with an objective of delivering a pharmacology dossier that substantiates the effectiveness of classical as well as novel Ayurvedic test articles Prepare Institutional Animal Ethics protocols and defend them in Institutional Animal Ethics Committee meetings. Prepare SOPs related to general experimental procedures and instruments. Ensure regular maintenance of equipment and instruments as per the facility’s schedule. Draft manuscripts for communication to scientific journals (with an IF of 2+). Requirements M.Pharm(Pharmacology)/M.V.Sc.(Veterinary Pharmacology)/PhD in Pharmacology with 2-3 years of industrial/academic experience. Demonstrated expertise in basic in vivo pharmacology techniques and assays, compound administration by different routes, blood withdrawal, animal necropsy and organ collection. Capability to work independently, within the project teams, and amongst different disciplines. Exceptional verbal, written communication and presentation skills. Excellent interpersonal skills. Patanjali Research Foundation is an equal opportunity employer and does not discriminate against any applicant because of race, colour, religion, gender, national origin, age and physical disability. How To Apply Write to jobs@patanjali.res.in with your detailed CV and career aspirations. Mention In Vivo Biologist in the subject field of your email. List three professional references other than your friends and family. Show more Show less

Excellent domain expertise and process knowledge of RCM for Hospital facility. Understanding of Hospital Facility IP DRG coding concepts, MS DRG, APR DRG, reimbursement methodology, ICD-10-CM, ICD-10-PCS guidelines, elements of UHDDS guidelines, query processes, documentation guidelines. Strong knowledge in human anatomy, physiology, pathophysiology, pharmacology, diagnostic studies, conservative and surgical treatments. Understanding of all document types, Operative Reports, Discharge Summary, Progress Notes, ED Report and all other report formats used in hospital care setting. Understanding of CMS IPPS payment methodologies Aware of consequences of risky practices like up-coding and down-coding, fraud and abuse, inflated documentation, OIG guidelines, and HIPAA rules. Skills Strong interpersonal skills, excellent communication skills, and ability to effectively work with and coach team members. Ability to communicate with other stakeholders and clients, MIS team, and training teams for driving quality management. Possess operational skills to manage team with better resource utilization. Should have an aptitude to learn new things. Ability to read, writes, and performs basic computer operations. Must be a self -starter, motivated, organized and able to prioritize tasks. Managing reports daily, weekly, monthly and monitoring and being active participant in client calls and maintaining good client relationship. Research, analyze and respond to inquiries regarding compliance, Show more Show less

Urgent requirement of Associate Professor Pharmacology Qualification- MD Pharmacology Salary- best in industry Eligibility- As Per NMC Job Types: Full-time, Part-time Schedule: Day shift Work Location: In person

Urgent requirement of Assistant Professor Pharmacology Qualification- MD Pharmacology Salary- best in industry Eligibility- As Per NMC Job Type: Full-time Schedule: Day shift Work Location: In person

Greetings from Venkateshwara Institute of Medical Sciences, Gajraula UP We are inviting applications from the all pre- para and clinical department who are looking for the full time. Giving the opportunity to explore the experience with us in the following Positions: Senior Resident/Assistant Professor/Associate Professor and Professor. #Generalmedicine #Generalsurgery #Anatomy #Biochemistry #Phsiology #Communitymedicine #Forensicmedicine #microbiology #Obstetrics & Gynaecology #pedaitrics #Ophthalmology #ENT #orthopedics #pharmacology #Anesthesiology Interested candidates Kindly approach Yashwant Singh on 9971796967 or email your resume at amr.vims@svu.edu.in Thanks & Regards Yashwant Singh HR VIMS, Gajraula

Location: [Lucknow, Shahjahanpur] Medical College Experience: Freshers to 20+ years Type: Full-Time | On-Site Notice Period: Immediate Joiners Preferred / Up to 1 Month Contact US - 8178692895 Email ID - effra@trimushr.com

Job Description :- Clinical Work Provide direct & indirect patient care in emergency care situations. Provide any & every detail about the procedures, medications, and answer patient queries & subsequent follow-up. Reporting & documenting USG findings/treatment plan in File/Portal. Documenting the prescribed mediation/Stimulation/HRT drugs etc. & in file/portal/ providing Trigger time. Executing all Donor Related Activity, in association with Donor Coordinator. Administer injection to patient/donor, as prescribed in file. Maintain stock of all required injections/drugs. Elicit accurate & relevant patient/donor medical history Co-ordinate procurement of necessary documents from patient/donor, per PCPNDT regulations. Update all patient records in both physical, as well as digital format. File all regulatory forms/consents before each procedure. Submit PCPNDT forms timely, as required by PCPNDT office. Identify & provide for physical, emotional, and developmental needs of patients. Counsel patients & their families; explain procedures planned for them. Ensure all procedures are carried out as per the SOP, and are compliant with the Policies on Universal Protection, Biomedical Hazard & Infection Control. Should have valid state registration Only immediate joiners apply for the role

Job Description :- Clinical Work Provide direct & indirect patient care in emergency care situations. Provide any & every detail about the procedures, medications, and answer patient queries & subsequent follow-up. Reporting & documenting USG findings/treatment plan in File/Portal. Documenting the prescribed mediation/Stimulation/HRT drugs etc. & in file/portal/ providing Trigger time. Executing all Donor Related Activity, in association with Donor Coordinator. Administer injection to patient/donor, as prescribed in file. Maintain stock of all required injections/drugs. Elicit accurate & relevant patient/donor medical history Co-ordinate procurement of necessary documents from patient/donor, per PCPNDT regulations. Update all patient records in both physical, as well as digital format. File all regulatory forms/consents before each procedure. Submit PCPNDT forms timely, as required by PCPNDT office. Identify & provide for physical, emotional, and developmental needs of patients. Counsel patients & their families; explain procedures planned for them. Ensure all procedures are carried out as per the SOP, and are compliant with the Policies on Universal Protection, Biomedical Hazard & Infection Control. Should have valid state registration Only immediate joiners apply for the role

Department-Centralised Monitoring Unit (CMU) Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can-do attitude with continuous improvement as one of your career objectives? Then we might have the right position for you. Apply now and join a growing team, working in an international environment. About the department The Centralised Monitoring Unit (CMU)- Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Medical reviewers) and technical programmers (Functional programmers, statistical monitors). Medical reviewers are actively involved in Risk-based medical monitoring in collaboration with the medical specialists from Denmark, with a focus on ensuring overall patient safety and wellbeing of all clinical trial participants, by ensuring compliance to protocol and identifying potential clinically significant outliers that require medical attention and medical data cleaning. The Functional Programmers develop operational visualizations in data visualization tools to support the trial teams on proactive centralized monitoring and Statistical Monitors perform the detection of unusual data patterns, systematic errors, and potential lack of compliance or fraud across trials. The Position: (NoteThis is not a role within Pharmacovigilance) The Senior Medical Reviewer is responsible for conducting comprehensive medical reviews of clinical trial data across various therapy areas within the drug development portfolio. This role ensures the highest quality and consistency of medical data, with a strong emphasis on patient safety, protocol adherence, and compliance with Good Clinical Practice (GCP), ICH guidelines, local regulations, and Standard Operating Procedures (SOPs). Key responsibilities include collaborating closely with study team members"”such as Data Managers, Trial Managers, and Medical Specialists"”throughout the trial process, providing timely updates on the status of medical reviews, and escalating any issues to maintain trial integrity and compliance. Responsible for contribution to or participation in trial planning activities related to medical review. Perform the quality check measure for the medical review. Responsible for clarifying and if possible, resolving issues of medical concern and inconsistencies in clinical trial data with staff at investigational sites. Responsible for presenting findings of Medical Review to relevant Medical Specialists to enable decision-making. Responsible for documenting medical reviews in the sponsor TMF. Ensure close collaboration with relevant study group members, especially the Data Manager, Trial Manager(s), and Medical Specialist during trial conduct. Provide training on the project and process to the new team members. Review and provide inputs to MMP as well as Medical Monitoring, Displays or other data listing required to perform Medical review. The input should ensure unambiguous monitoring requirements as well as medical monitoring displays and data listing to enable efficient medical review. Qualifications: A graduate degree in Medicine or a related field is required (MBBS & MD in Pharmacology preferred; MBBS & MD in other clinical or paraclinical areas with relevant experience in clinical patient management or clinical research will also be considered). Preferably 3-5 years of relevant experience in Clinical Drug Development (Medical Data Review, Medical Monitoring, Investigator, Safety Surveillance, Scientific Clinical Drug Development etc). 1-2 years of project management experience is essential. Solid understanding of ICH (International Council for Harmonisation) guidelines and GCP (Good Clinical Practice) principles. Proficient in computer applications, including MS Office, MS Project, and PowerPoint. Strong grasp of medical terminology and clinical trial processes. Demonstrated analytical skills with a results-oriented approach. Exceptional proficiency in written and spoken English.

Roles and Responsibilities Interpret diagnostic imaging results from various modalities such as CT scan, MRI, ultrasound, mammography, and X-rays. Conduct Doppler studies to evaluate blood flow and identify abnormalities. Perform sonography procedures to visualize internal organs and tissues. Collaborate with other healthcare professionals to develop treatment plans based on radiological findings. Stay up-to-date with latest advancements in medical imaging technology and best practices. Desired Candidate Profile 0-2 years of experience in Radiology or related field (freshers can apply). Strong knowledge of pharmacology, radiation safety, and medical terminology. Proficiency in performing various diagnostic tests including CT scans, MRI scans, ultrasounds, mammographies, MRIs etc. . Ability to work effectively under pressure during emergency situations.

Excellent domain expertise and process knowledge of RCM for Hospital facility. Understanding of Hospital Facility IP DRG coding concepts, MS DRG, APR DRG, reimbursement methodology, ICD-10-CM, ICD-10-PCS guidelines, elements of UHDDS guidelines, query processes, documentation guidelines. Strong knowledge in human anatomy, physiology, pathophysiology, pharmacology, diagnostic studies, conservative and surgical treatments. Understanding of all document types, Operative Reports, Discharge Summary, Progress Notes, ED Report and all other report formats used in hospital care setting. Understanding of CMS IPPS payment methodologies Aware of consequences of risky practices like up-coding and down-coding, fraud and abuse, inflated documentation, OIG guidelines, and HIPAA rules. Skills: Strong interpersonal skills, excellent communication skills, and ability to effectively work with and coach team members. Ability to communicate with other stakeholders and clients, MIS team, and training teams for driving quality management. Possess operational skills to manage team with better resource utilization. Should have an aptitude to learn new things. Ability to read, writes, and performs basic computer operations. Must be a self -starter, motivated, organized and able to prioritize tasks. Managing reports daily, weekly, monthly and monitoring and being active participant in client calls and maintaining good client relationship. Research, analyze and respond to inquiries regarding compliance,

II We are Hiring II Pharmacology - Assistant Professor Teach medical students in the classroom and clinical settings Participate in academic activities such as seminars, conferences, and workshops Supervise and mentor junior residents and medical students Perform administrative tasks as assigned by the department head Monitoring and providing general care to patients on hospital wards and in outpatient clinics. Admitting patients requiring special care, followed by investigations and treatment. Examining and talking to patients to diagnose their medical conditions. Teaching and supervising junior doctors and medical students. Qualification - MBBS, MD Free Accommodation within Campus Salary - 20 L - 24 L (Negotiable) Share CV @ hr@amrach.com Thanks & Regards; Amrach Consulting Services LLP Call@ 9105521331 WhatsApp@ 9105521331

Teaching undergraduate and graduate courses in pharmacology, conducting research, and supervising student Supervise and mentor undergraduate and graduate students in their research and academic development.

We require doctors for Medical Colleges & Hospitals PAN India Qual: MD/MS, DNB, (All Dept) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Jyoti Call/Whatsapp: 7973500988 weps.recruitments@gmail.com

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

Designations : Senior Resident Assistant Professor, Associate Professor, Professor. Role & responsibilities Assistant Professor Responsibilities: Assisting with various departmental duties and providing academic support to Professors and other staff. Recruiting, training, and mentoring new TAs and other junior staff. Conducting research and publishing papers in academic journals. Representing the university at conferences and delivering presentations when necessary. Teaching and supervising undergraduate and graduate students. Providing demonstrations and supervising experiments and investigations. Answering questions in class or via email or telephone. Providing Professors and Department Heads with feedback on student progress. Writing proposals to secure funding for research. Attending faculty and departmental meetings and voicing concerns or providing suggestions for improvement. Associate Professor Responsibilities: Developing and delivering course material, curricula, and syllabi. Assisting with the training and recruitment of new lecturers, teaching assistants, and Professors. Conducting research, publishing papers, and attending conferences. Attending academic events and networking with other researchers and field experts. Supervising, advising, and mentoring teaching assistants and graduate students. Participating in faculty and departmental meetings. Shortlisting, interviewing, and selecting students for graduate programs. Organizing guest seminars and faculty events where students can interact with established industry professionals. Traveling to other higher education settings to gain experience and expand networks. Writing proposals to secure research funding. Professor Responsibilities: Developing curricula and delivering course material. Conducting research, fieldwork, and investigations, and writing up reports. Publishing research, attending conferences, delivering presentations, and networking with others in the field. Traveling to other universities or academic settings to participate in learning opportunities and gain experience. Participating in committee, departmental, and faculty meetings. Providing training and mentoring to teaching assistants and junior lecturers. Reviewing methods and teaching materials and making recommendations for improvement. Assisting with student recruitment, interviews, and academic counseling sessions. Contributing to the creation of an environment that promotes growth, equality, and freedom of speech. Designations : Senior Resident Assistant Professor, Associate Professor, Professor. Location : Lb Nagar Hyderabad Further Details : 9490294856 Mail ID - recruitment@kaminenihospitals.com

Urgent requirement of Associate Professor Pharmacology Qualification- MD Pharmacology Salary- Best in industry Eligibility- As Per NMC Norms Job Type: Full-time Schedule: Day shift Work Location: In person

A reputed medical college and hospital in Banthra, Shahjahanpur (U.P.) invites applications from eligible candidates for faculty positions across multiple departments. Walk-in interviews are held every Tuesday from 09:00 AM to 02:00 PM at the Principal Office, Ground Floor . We are hiring for the following teaching positions: Professor Associate Professor Assistant Professor Senior Resident Departments with Openings Anatomy Physiology Biochemistry Pharmacology Pathology Microbiology FMT Community Medicine General Medicine Paediatrics Dermatology (Skin) Psychiatry General Surgery Orthopaedics ENT Ophthalmology Obstetrics & Gynaecology Anaesthesia Radiology Eligibility CriteriaSenior Resident Qualification: MD/MS/DNB Experience: Freshers eligible Assistant Professor Qualification: MD/MS/DNB Experience: 1 year Senior Residency in the same department Associate Professor Qualification: MD/MS/DNB Experience: 4 years as Assistant Professor + 2 paper publications + MEU + BCMR Professor Qualification: MD/MS/DNB Experience: 3 years as Associate Professor + 2 paper publications + MEU + BCMR Note: Eligibility as per the latest amendment of NMC regulations. Akash HR Manager akash@medicohire.com || 90 637 637 34 Medico Hire || www.medicohire.com Job Type: Full-time Pay: ₹250,000.00 - ₹300,000.00 per month Benefits: Cell phone reimbursement Flexible schedule Leave encashment Provident Fund Schedule: Day shift Morning shift Rotational shift Language: English (Preferred) Work Location: In person

Clinical Pharmacist || Work life balance (Only Graduates Can Apply, Max age require- 33 Yrs.) || Near Gurgaon. **NOTE** - Pharmacy Council registration/ Registration applied slip (acknowledgement) is mandatory . Educational Qualification: Pham D (Doctor of Pharmacy). - Preferable. M.Pharma (Done in either Pharmacology or Pharmacy Practice) B.Pharma (Done in either Pharmacology or Pharmacy Practice) Fresher can also apply. Job Description: - To ensure medication & patient safety by appropriately following hospital policies & regulatory / accreditation related guidelines 1. Before Administration, Medication review and clinical audits on the floor. 2. Transcription / Indenting of drug and non-drug orders. 3. Responsible for medication tracking and receiving from pharmacy. 4. Auditing all the in-patient orders for drug name, strength, formulation, dosage and duration of therapy, therapeutic duplication and to check for possible drug interaction, if any as per hospital protocols. 5. Checking the Medication Administration Records in the ward and rectification of any medication error observed. 6. For clarification check the patient record at the ward / ICU discuss with Clinical Pharmacologist. 7. In case any non-formulary drugs are indented inform to the concerned doctor and substitute it with the drugs given in the formulary. 8. Responsible for checking the drugs in impress stock, crash cart, disaster kits and ambulance regularly. 9. Responsible for documentation of restricted antibiotics and report it to Clinical Pharmacologist. 10. Monitoring of adverse drug reaction. 11. Drug information resource. Note: Pharmacy Council registration/ Registration applied slip (acknowledgement) is mandatory . Rotational shifts (including nights). Job Types: Full-time, Permanent, Fresher Pay: ₹22,000.00 - ₹30,000.00 per month Benefits: Commuter assistance Health insurance Leave encashment Life insurance Paid sick time Paid time off Provident Fund Schedule: Day shift Evening shift Morning shift Night shift Rotational shift Supplemental Pay: Overtime pay Performance bonus Work Location: In person

Male M.Pharm Faculty for Pharmacy College at Patna, Bihar Role and Responsibilities: Teaching and Curriculum Development: - Deliver lectures and facilitate discussions on various topics in pharmacy, such as pharmacology, pharmaceutical sciences, clinical pharmacy, and pharmacy practice. Develop and update course syllabi, instructional materials, and assessments to ensure alignment with program goals and objectives. Utilize innovative teaching methods, technology, and active learning strategies to enhance student engagement and learning outcomes. Provide academic advising and mentorship to students, including guidance on career paths and research opportunities. Research and Scholarship: - Conduct original research in areas related to pharmacy practice, drug development, pharmaceutical sciences, or other relevant fields. Publish research findings in reputable peer-reviewed journals and present at national and international conferences. Collaborate with colleagues, industry partners, and healthcare professionals on research projects and grants. Stay abreast of emerging trends, advancements, and best practices in pharmacy through continuous professional development. Service and Leadership: - Participate in departmental, college, and university committees, meetings, and events. Contribute to the development and evaluation of the pharmacy program's curriculum, policies, and accreditation processes. Engage in community outreach activities, such as health fairs, educational programs, and collaborations with local healthcare organizations. Foster positive relationships with students, faculty, preceptors, and professionals within the pharmacy field. Good Communication Skills Qualification: M.Pharm from any reputed University Experience: 3 - 5 Years Salary: Negotiable Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Schedule: Day shift Language: English (Preferred) Work Location: In person

Job Title: Assistant Professor – Cardiovascular Technology Job Summary: We are seeking a highly skilled and motivated Assistant Professor Cardiovascular Technology to teach, guide, and inspire students in the field of cardiovascular health, diagnostic technology, and medical procedures. The ideal candidate will have a strong clinical background, a passion for education, and a commitment to research excellence. This position offers an opportunity to shape the future of cardiovascular technologists through innovative teaching, clinical training, and active participation in academic research. Key Responsibilities: 1. Teaching and Instruction: - Deliver high-quality instruction in cardiovascular technology courses, including topics such as cardiovascular anatomy, physiology, electrocardiography (ECG), echocardiography, invasive and non-invasive diagnostic procedures, and cardiac pharmacology. - Develop and update course content, lecture materials, and laboratory exercises in accordance with current cardiovascular practices and technologies. - Create an engaging learning environment utilizing both traditional and technology-enhanced teaching methods. - Assess student performance through exams, quizzes, lab work, projects, and clinical evaluations. 2. Clinical Training and Supervision: - Oversee and guide students in clinical settings, ensuring proper application of cardiovascular technology in real-world scenarios. - Supervise and mentor students during clinical internships, providing feedback on their performance and helping them develop professional skills. - Ensure that students follow safety, ethical, and clinical protocols while interacting with patients in a clinical setting. 3. Research: - Engage in original research in the field of cardiovascular technology, including innovations in diagnostic procedures, technologies, and patient care. - Publish research findings in peer-reviewed journals and present at relevant academic and professional conferences. - Actively seek out research grants and opportunities for collaboration with industry or other academic institutions. - Encourage and involve students in research projects and foster an academic culture of inquiry. 4. Curriculum Development: - Contribute to the development and review of the Cardiovascular Technology curriculum, ensuring that it aligns with industry standards, accreditation requirements, and emerging trends in healthcare. - Stay current with technological advancements in cardiovascular healthcare and integrate them into the curriculum. - Review and update course syllabi regularly to maintain academic rigor and relevance. 5. Student Mentorship and Advising: - Provide academic and career counselling to students in the cardiovascular technology program. - Advise students on internship opportunities, job placement, and certification preparation. - Serve as a mentor for students, guiding them in their professional development and offering support for both academic and personal growth. 6. Academic Administration: - Participate in departmental meetings, committees, and university events. - Contribute to institutional development and accreditation processes related to the Cardiovascular Technology program. - Maintain student records, grades, and other academic documentation as required. 7. Professional Development: - Actively engage in continuing education and professional development to stay up-to-date with advancements in cardiovascular technology and teaching methodologies. - Attend workshops, seminars, and conferences to enhance knowledge in both cardiology and educational practices. Qualifications: - Master’s or Doctorate in Cardiovascular Technology, Cardiology, or a related field. - Certification in Cardiovascular Technology or related certifications (e.g., Registered Cardiovascular Invasive Specialist [RCIS], Registered Diagnostic Cardiac Sonographer [RDCS], etc.) is required. Experience: - At least 2–3 years of clinical experience in cardiovascular technology or related healthcare field. - Teaching experience in a higher education setting is preferred. - Experience with curriculum development and student assessment is a plus. Skills: - Strong knowledge of cardiovascular diagnostic technologies, including ECG, echocardiography, and cardiac catheterization. - Ability to explain complex cardiovascular topics in an engaging and understandable manner. - Familiarity with clinical practice and patient care in cardiovascular settings. - Proficiency with educational technology and learning management systems. - Strong communication, organizational, and interpersonal skills. Job Type: Full-time Work Location: In person