1075 Pharmacology Jobs - Page 14

Date: 1 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Dedicated Centre Job Description Designation: Associate Scientist / Senior Associate Scientist Job Location: Bangalore Department: TM-TDDT About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Job Purpose (1-2 Lines) We are seeking motivated master’s level scientists (MS, MTech, MSc, etc) to join the Translational Medicine team at the Biocon Bristol Myers Squibb Research Center in Bangalore, India. Key responsibilities of this role are to serve as an execution arm for the preclinical support of asset programs through mechanism of action-based studies, differentiation from standard of care and competitive therapeutics, combination rationale, new indications (life cycle management), and patient selection strategies. S/He will work directly with translational scientists, disease leaders within translational medicine, and will also interact with thematic research centers in early development within the company. Key Responsibilities Conduct preclinical/laboratory experiments on late stage BMS portfolio compounds to support annual goals and objectives for Translational Medicine (for internal /external, collaborations, compound specific plans etc). Responsible for delivering data in support of translational strategies including biomarkers, patient selection hypotheses, dose and schedule, combination strategies, resistance mechanisms and differentiation. Interfaces with TM scientists across departments to ensure seamless flow of information for assets which are entering the remit of translational medicine. Assists in designing experiments and delivering data for collaborative projects along with TM scientists. Maintains comprehensive records, communicates regularly and makes presentations within the department, as required. Reports experimental finding in written nonclinical pharmacology study reports, to support regulatory filings. Educational Qualification Masters with at least 2 years of relevant work experience across immunology, oncology, heme-oncology focus areas. Industry experience is a plus. Multiple positions can range upto 6 years of experience. Technical/functional Skills Cell culture, primary cell isolation, cell transfection and single cell cloning; including siRNA / CRISPR / TALEN or HDR workflows Gene expression methods including qRT-PCR and/or familiarity with RNA sequencing, epigenomic methods including methylation analysis, ChIP etc Protein analyses and immunoassays, and cell phenotyping analysis (e.g. ELISA, MSD, Luminex, TSA, CBA, flow cytometry). Design, setup and execution of autoimmune, solid tumor oncology or heme-oncology in vivo pharmacology models. Excellent verbal and written communication skills, familiarity with standard or relevant software platforms, and scientific qualities are expected. Competence in analysis and solving of problems, keeping track of overall goals. Maintain a good understanding of the methodological basis and biological significance of assays performed. Forecast potential issues regarding support of assays for current and long term projects. Devise strategic solutions to identified and potential hurdles/issues and efficiently and proactively troubleshoot technical and experimental problems. Experience 2-6 years Behavioral Skills A self-starter, who is/can become technically proficient in a diverse set of techniques and assays with a focus on quality and speed, and will meticulously follow internal SOPs Good basic lab skills required (pipetting, balances, etc.) Highly detailed and meticulous, high standards of data entering and QC Must be highly adaptive to changing timelines and goals Must be comfortable taking on complex tasks with minimal direct supervision An excellent multitasker with an ability to be level-headed in a fast-paced lab setting Team-oriented and comfortable working in a highly dynamic matrix environment across multiple locations Prior experience working with patient samples (i.e. FFPE tissue, Fresh Frozen tissue, blood) or working in a CLIA/GCLP/clinical environment is a plus Must be comfortable and able to work with animal (rodent) or human derived samples Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Scientific Content Writer (Intern) Duration: 3–6 months About HaystackAnalytics HaystackAnalytics is a genomics-based health tech company, revolutionizing infectious disease diagnostics, personalized medicine, and public health through cutting-edge technologies like Next-Generation Sequencing (NGS). Our flagship product Infexn™ is transforming how infections are diagnosed and treated across India. Role Overview We are looking for a Scientific Content Writing Intern who can help translate complex scientific data into clear, accurate, and engaging content. This role is ideal for students or early-career professionals passionate about science communication, public health, and genomics. Key Responsibilities Assist in writing, editing, and proofreading scientific documents including: Scientific content for blog posts, case studies, product brochures, and posters Whitepapers and abstracts for scientific conferences Website and social media content related to genomics and diagnostics Conduct literature reviews and ensure content accuracy and alignment with current scientific understanding Collaborate with R&D, and clinical teams to gather data and insights Maintain referencing and citations in appropriate formats (e.g., AMA, Vancouver) Support development of visual science communication tools like infographics Requirements Master’s or final year Bachelor's student in life sciences, biotechnology, microbiology, genetics, pharmacology, or a related field Excellent written and verbal communication skills Strong understanding of biology/genomics and interest in diagnostics or healthcare innovation Ability to interpret and simplify research findings for broader audiences Familiarity with literature databases (e.g., PubMed) and reference managers (e.g., Mendeley/Zotero) What You’ll Gain Hands-on experience at the intersection of science, technology, and healthcare Mentorship from experienced medical writers, scientists, and clinicians Opportunity to publish or contribute to high-visibility content and campaigns Potential for full-time opportunities based on performance Note: This is a paid internship.Skills: editing,literature review,scientific writing,healthcare,communication,healthcare innovation,data analysis,proofreading,genomics,science communication,genomics understanding,life sciences knowledge,visual communication,writer

Job description Applications are invited for the faculty positions We are looking for Senior Resident, Assistant Professor, Associate Professor, professor And Consultant. JOB LOCATION -TAMIL NADU 1. Senior Resident Anatomy, Paediatrics, Biochemistry, Forensic Medicine, General Medicine, Radiology , Obstetrics & Gynaecology, General Surgery, Microbiology, Pharmacology, Physiology, Community Medicine, Pathology, Respiratory medicine, Emergency Medicine.Anesthesia,Ophthalmology,Orthopaedics,Psychiatry, Dermatology. 2. Assistant Professor Anatomy, Paediatrics, Biochemistry, Forensic Medicine, General Medicine, Radiology , Obstetrics & Gynaecology, General Surgery, Microbiology, Pharmacology, Physiology, Community Medicine, Pathology, Respiratory medicine, Emergency Medicine.Anesthesia,Ophthalmology,Orthopaedics, Psychiatry, Dermatology. 3. Associate Professor Anatomy, Paediatrics, Biochemistry, Forensic Medicine, General Medicine, Radiology , Obstetrics & Gynaecology, General Surgery, Microbiology, Pharmacology, Physiology, Community Medicine, Pathology, Respiratory medicine, Emergency Medicine.Anesthesia,Ophthalmology,Orthopaedics, Psychiatry, Dermatology,ENT. 4. Professor Anatomy, Paediatrics, Biochemistry, Forensic Medicine, General Medicine, Radiology , Obstetrics & Gynaecology, General Surgery, Microbiology, Pharmacology, Physiology, Community Medicine, Pathology, Respiratory medicine, Emergency Medicine.Anesthesia,Ophthalmology,Orthopaedics, Psychiatry, Dermatology,ENT. 5.CONSULTANT - Cardiologist - Radiologist - Surgical Gastro - Gynaecology - Microbiology - Pathology Kindly Share your cv to 8428096996 M - 8428096996 Contact Person - G Sathya Qualification: As per NMC Norms.. Remuneration: As per qualification & Experience.. Location: - Tamil Nadu

Company Description CT Group of Institutions is a leading educational group committed to excellence in education and overall well-being. The group includes a wide range of institutions from pre-schools to postgraduate institutes, offering world-class infrastructure, Wi-Fi enabled campuses, well-equipped libraries, and advanced laboratories. Supported by experienced academicians, CT Group offers an ideal environment for education across various fields, including Engineering, Architecture, Management, Pharmacy, IT, Hotel Management, and more. Located in Jalandhar, the institutions aim to provide education that is at par with the best in the world. Role Description This is a full-time, on-site role for Professor, Associate Professor, and Assistant Professor of Pharmaceutics and Pharmacology, located in Jalandhar. The role includes developing and delivering curriculum, mentoring students, conducting research, publishing articles, collaborating with other departments, and participating in academic events. The faculty members will also engage in administrative duties and contribute to the growth and development of the department. Qualifications Proficiency in Pharmaceutics and Pharmacology Experience in research and academic publishing Strong teaching and mentoring skills Effective communication and interpersonal skills Ability to collaborate with other departments Experience in curriculum development and academic administration Ph.D. in Pharmaceutics, Pharmacology, or a related field Previous teaching experience at the college or university level is preferred Commitment to staying updated with advancements in the field

Interested canddiates may come for Walk-In Interview as per below details- Position - Clinical Pharmacist Date of Interview - 10th & 11th Jul 2025 Reporting Time - 10 am Venue Medanta Hospital, Amar Shaheed Path, Sushant Golf City, Lucknow (LG Floor Area Admin Block (HR Department) Role & responsibilities 1. Checking the Medication Administration Records in the ward and rectification of any medication error observed. 2. For clarification check the patient record at the ward / ICU discuss with Clinical Pharmacologist. 3. In case any non-formulary drugs are indented inform to the concerned doctor and substitute it with the drugs given in the formulary. 4. Responsible for checking the drugs in impress stock, crash cart, disaster kits and ambulance regularly. 5. Responsible for documentation of restricted antibiotics and report it to Clinical Pharmacologist 6. Monitoring of adverse drug reaction. 7. Drug information resource. Preferred candidate profile B. Pharma / M. Pharma / Pharma D. / (Fresher OR Experienced) Great interpersonal skills and team work ability. Good analytical skills and quick thinking. Good knowledge of medicines. Should have knowledge to work on Computer

Urgent Requirement of MD/MS doctors for Medical Colleges all over India

Akshara Consultancy - Laboratory Items Distribution Company Qualifications: Bachelors degree,or masters preferably Pharmaceutics, or Pharmacology 2-3 years of sales experience, preferably in pharmaceutical laboratory items. Key Responsibilities: Sell laboratory items, including microbiology and chromatography products (HPLC/GC vials and columns). Develop and expand client relationships. Conduct regular field visits to follow up with clients and secure orders. Maintain and enhance sales performance for both existing and new business. Travel across Telangana to meet clients and ensure customer satisfaction. Desired Skills and Attributes: Strong interpersonal and communication skills. Ability to work independently and manage time effectively. Self-motivated with a proactive sales approach. Willingness to travel extensively within the region.

Job Title: Senior Pharmacist Company Name: Manipal Hospitals Job Description: As a Senior Pharmacist at Manipal Hospitals, you will play a critical role in delivering high-quality pharmaceutical care to patients. You will be responsible for managing the pharmacy department, overseeing medication distribution, ensuring compliance with healthcare regulations, and providing expert medication counseling to healthcare professionals and patients. Your role will involve collaborating closely with interdisciplinary teams to optimize therapeutic outcomes and enhance patient safety. Key Responsibilities: - Oversee the daily operations of the pharmacy department, including medication preparation, dispensing, and inventory management. - Ensure compliance with all legal, regulatory, and accreditation requirements related to pharmacy operations. - Provide clinical pharmacy services including medication therapy management, drug utilization review, and formulary management. - Assist in the training and mentoring of junior pharmacists and pharmacy staff. - Evaluate and verify medication orders for accuracy, appropriateness, and safety. - Educate healthcare professionals and patients about medication therapies, including proper administration and potential side effects. - Conduct medication reconciliation to ensure continuity of care for patients. - Participate in quality improvement initiatives and contribute to patient safety programs. - Stay updated with the latest developments in pharmacy practice, pharmacotherapy, and drug information. Skills Required: - Strong knowledge of pharmacology, therapeutics, and pharmacy regulations. - Excellent clinical judgment and decision-making abilities. - Good communication and interpersonal skills for effective patient and team interaction. - Strong organizational skills with the ability to prioritize tasks effectively. - Proficiency in using pharmacy management software and electronic health records (EHR). - Adept at conducting clinical assessments and evaluating patient medication regimens. - Commitment to continuous learning and professional development. Tools Required: - Pharmacy management systems (e.g., Pyxis, Meditech). - Electronic health records (EHR) systems. - Drug information databases (e.g., Micromedex, Lexicomp). - Medication therapy management software. - Inventory management tools and software. - Standard office software (e.g., Microsoft Office Suite). This position requires a dynamic individual with a strong commitment to patient care and a collaborative approach to healthcare. Join us at Manipal Hospitals and be part of a team dedicated to providing exceptional pharmaceutical services. About the Role: As a Senior Pharmacist at Manipal Hospitals, you will play a vital role in ensuring optimal medication management for patients. You will be responsible for overseeing pharmacy operations, ensuring compliance with regulatory standards, and providing expert guidance on pharmacotherapy to healthcare providers. You will also participate in clinical rounds and collaborate with multidisciplinary teams to enhance patient care. About the Team: You will be part of a dynamic and collaborative team that includes fellow pharmacists, pharmacy technicians, and healthcare professionals committed to patient safety and medication efficacy. The team values continuous learning and innovation, working together to improve pharmaceutical care services across the hospital. A supportive work environment fosters professional development and knowledge sharing. You are Responsible for: - Managing medication therapy and ensuring the safe dispensing of pharmaceuticals. - Conducting medication reconciliation and providing consultations to healthcare providers. - Developing and implementing pharmacy policies and procedures to enhance service delivery. - Supervising pharmacy staff and ensuring their adherence to best practices. - Monitoring drug utilization patterns and conducting quality improvement initiatives. To succeed in this role - you should have the following: - A Bachelor s or Doctor of Pharmacy (PharmD) degree from an accredited institution. - Valid pharmacy license and relevant clinical experience in a hospital setting. - Strong knowledge of pharmacology, therapeutics, and medication management. - Excellent communication and interpersonal skills to work effectively with multidisciplinary teams. - A commitment to continuous professional development and staying updated on pharmaceutical advancements.

Job Role: Senior Resident Location: Gujarat Experience: 0 - 1 Years Salary: 1.10 L/Mo - 1.20 L/Mo; negotiable Language Skills: Essential: English Desirable: Gujarati / Hindi Gender: Male / Female Required Candidate profile Education: UG: MBBS or equivalent as per NMC rules PG: MD/DNB (Pharmacology) or equivalent Eligibility: As per NMC rules Accommodation Details: Accommodation Provided Perks and benefits Salary Negotiable, Accommodation Provided

#MDPharmacology Greetings from India Pharma People A leading Pharma major is looking for a Medical Advisor based at their corporate office in Mumbai Candidate essentially need to be MD Pharmacology have exposure to Medico Marketing with leading Pharma Major The JD would be as Product Launch Conduct comprehensive literature search, prepare medical manuals and Power point slides. New Product Launch Presentation to the Marketing team and field force with technical inputs on therapy area and product details. Responding to Queries Ensure good customer relations by addressing queries from field force and doctors along with relevant scientific support. Scientific Support to the Brands Keep abreast of the latest scientific information on products, therapy areas, landmark trials, guidelines from scientific associations on therapy areas Provide technical support to the Marketing/Sales Department in terms of references on new as well as existing products. Prepare prescribing Information. Validate medical content in marketing inputs for accuracy and high scientific quality. Organize CME (Continuing Medical Education) Kits including Power point slide presentation and important references. Please share your CV at ipp@indiapharmapeople.com oe whatsApp at 9767790833 Regards Jai Hind Satish Sanhotra 9767790833

We are looking for a licensed and detail-oriented Pharmacist to join our healthcare team. The ideal candidate will be responsible for dispensing medications, providing expert advice on prescription use, and ensuring patient safety by reviewing potential drug interactions. Key Responsibilities: Accurately dispense prescription medications to patients Provide information and guidance on drug usage, dosage, interactions, and side effects Review and interpret prescriptions from doctors and other medical professionals Ensure compliance with all pharmacy laws and regulations Maintain proper storage and security conditions for medications Oversee and manage inventory of pharmaceuticals Provide vaccination and health screening services (if applicable) Maintain patient records and handle insurance claims Counsel patients on lifestyle changes and wellness programs as needed Supervise and train pharmacy assistants and technicians Qualifications: Bachelor's or Doctor of Pharmacy (PharmD) degree Proven experience as a pharmacist is preferred Strong knowledge of pharmacology and drug interactions Excellent communication and customer service skills High attention to detail and accuracy Familiarity with pharmacy software and systems Work Schedule: Flexible working hours Weekend or shift flexibility may be required Benefits: Competitive salary Paid time off Medical insurance Ongoing training and development Supportive work environment Job Type: Full-time Pay: ₹10,000.00 - ₹20,000.00 per month Work Location: In person

Pharmacist Location:- Shree Siddhivinayak Cancer Hospital, Miraj. Designation: Pharmacist Work Experience: 1-4 Years in Retail / Hospital Attached Medical Store Job Description: Dispensing prescribed drugs as per physicians instructions / hospital’s indent. Pharmacist attend to patients, manage high volume of prescriptions & get involved in operational activities. Check prescriptions to ensure that there are no errors & that they are appropriate & safe for the individual/ patient as per their need. Contacting referring physicians with the questions regarding prescription. Handle customer complaints/ queries & counselling/ resolving patient’s issues, whenever needed. Comply with all applicable rules and regulations of D&C Act and SOPs of the organization. Participate in daily / weekly / monthly stock checking processes & separate expired medicines on a periodic basis. Oversee & maintain a safe & clean working environment. Contributing to team effort by accomplishing related results as needed. Completing pharmacy operational requirements by organizing & directing workflow. Verifying bill entries, charges, discounts, inspections & tally with the cash inflow of each day. Requirements: 1. D. Pharm/ B. Pharm/ M. Pharm. From an accredited university. 2. Pharmacist License Critical Skills: 1. Analyzing information & stock time to time 2. Administering medication 3. Verbal communication 4. Pharmacology 5. Managing Process 6. Quality service 7. Attention to detail 8. Team work 9. Coordination 10. Professional Ethics Job Types: Full-time, Permanent, Fresher Pay: From ₹250,000.00 per year Benefits: Cell phone reimbursement Health insurance Leave encashment Life insurance Paid time off Provident Fund Schedule: Day shift Evening shift Morning shift Night shift Rotational shift Supplemental Pay: Overtime pay Performance bonus Shift allowance Yearly bonus Education: Diploma (Required) Experience: Total: 1 year (Required) Hospital Pharmacist: 1 year (Required) License/Certification: Pharmacist License (Maharashtra Council) (Required) Location: Miraj, Maharashtra (Required) Shift availability: Day Shift (Required) Night Shift (Required) Work Location: In person

Summary To write, review and manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. To provide authoritative documentation-related consultancy to other line functions. To coach, mentor and train less experienced writers. About The Role Major accountabilities: To author, review and/or independently manage high quality clinical and safety documents: complex Clinical Study Reports (CSR), Risk Management Plans (RMP), complex CTD submission documents (clinical overviews, summaries of clinical efficacy and safety, summaries of clinical pharmacology and biopharmaceutics), other documents for health authorities (e.g., Briefing Books, answers to questions). Lead writing team for complex submissions, actively contributing to key messaging and pooling strategy, providing expert content guidance for clinical portions of the CTD, and ensuring compliance of documentation to internal company standards and external regulatory guidelines. Input into planning of data analyses and presentation (statistical analysis plan review and meetings) used in CSRs, submission documents and/or answers to questions. Documentation expert in GCTs and CSTs to ensure compliance to internal company standards and external regulatory guidelines. Provide content and strategic expertise for clinical portions of the CTD. Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Key Performance Indicators Delivery of high quality clinical and safety documents in time and in compliance with internal and external standards -Customer / partner/ project feedback and satisfaction -Adherence to Novartis policy and guidelines Minimum Requirements Work Experience: Functional Breadth. Project Management. Collaborating across boundaries. Operations Management and Execution. Representing the organization. Skills Clinical Research. Clinical Trials. Detail Oriented. Medical Writing. People Management. Project Management. Regulatory Compliance. Safety. Languages English. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Summary To write, review and manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. To provide authoritative documentation-related consultancy to other line functions. To coach, mentor and train less experienced writers. About The Role Major accountabilities: To author, review and/or independently manage high quality clinical and safety documents: complex Clinical Study Reports (CSR), Risk Management Plans (RMP), complex CTD submission documents (clinical overviews, summaries of clinical efficacy and safety, summaries of clinical pharmacology and biopharmaceutics), other documents for health authorities (e.g., Briefing Books, answers to questions). Lead writing team for complex submissions, actively contributing to key messaging and pooling strategy, providing expert content guidance for clinical portions of the CTD, and ensuring compliance of documentation to internal company standards and external regulatory guidelines. Input into planning of data analyses and presentation (statistical analysis plan review and meetings) used in CSRs, submission documents and/or answers to questions. Documentation expert in GCTs and CSTs to ensure compliance to internal company standards and external regulatory guidelines. Provide content and strategic expertise for clinical portions of the CTD. Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Key Performance Indicators Delivery of high quality clinical and safety documents in time and in compliance with internal and external standards -Customer / partner/ project feedback and satisfaction -Adherence to Novartis policy and guidelines Minimum Requirements Work Experience: Functional Breadth. Project Management. Collaborating across boundaries. Operations Management and Execution. Representing the organization. Skills Clinical Research. Clinical Trials. Detail Oriented. Medical Writing. People Management. Project Management. Regulatory Compliance. Safety. Languages English. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Job Role: Professor Location: Gujarat Experience: 8 - 12 Years Salary: 3.25 L/Mo - 3.75 L/Mo; negotiable Language: Essential: English Desirable: Gujarati / Hindi Gender: Male / Female Required Candidate profile Education: UG: MBBS or equivalent as per NMC rules PG: MD / DNB (Pharmacology) or equivalent Accommodation Details (if Provided): Accommodation Provided Perks and benefits Salary Negotiable, Accommodation Provided

We are currently hiring for Medical Coding Trainer with minimum 5 Years of experience into Medical Coding Prior experience training medical coding batches in a classroom or group setting is required. Strong background in ICD-10, CPT, and HCPCS Required Candidate profile Proven ability to design and lead group training sessions, including interactive learning activities and performance evaluations. CPC (Certified Professional Coder) certification required.

Summary Of Responsibilities Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits. Prepares and implements project plans related to Clinical Monitoring responsibilities. Ensures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements. Safeguards data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems. Confirms Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial. Guarantees that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements. Ensures adherence to global quality control and CRA performance metrics. Ensures audit readiness at site level. Acts in the project role of a Lead CRA as assigned. General On-Site Monitoring Responsibilities: Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study. Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements. Ensure the integrity of the source data reported by careful source document review. Monitor data for missing or implausible data. Ensure study data completeness, accuracy, consistency, and compliance; identify deficiencies, deviations and discrepancies, and initiate corrective action as required. Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy. Travel, including air travel, may be required and is an essential function of the job. Prepare and submit accurate and timely trip reports. Independently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision, on Fortrea or client data management systems, as assigned by management. Assist with the administration of clinical research projects, recruiting investigators (if applicable), collecting investigator documentation and site management. Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems. Track IP shipments and supplies, as needed. Track and follow-up on serious adverse events as assigned. Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met. Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned. Attend investigators’ meetings (if applicable), project team meetings and teleconferences, and others as needed. Present training content for site initiation. Assist with training of new employees (e.g., co-monitoring). All other duties as needed or assigned. Qualifications (Minimum Required) University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate. Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements. Thorough knowledge of monitoring procedures. Basic understanding of the clinical trial process. Fluent in local office language and in English, both written and verbal. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Experience (Minimum Required) University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). AND A minimum of 3 years of Clinical Monitoring & Oncology experience. Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines. Ability to work with minimal supervision. Have an understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs. Good planning, organization, and problem-solving abilities. Works efficiently and effectively in a matrix environment. Preferred Qualifications Include Thorough working knowledge of Fortrea SOPs for site monitoring. One (1) or more additional years of experience in a related field (i.e., medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred. Phase I monitoring experience. Life Science or Nursing qualification. Specific skills, systems, certifications, and/or licenses preferred. Personal characteristics (leadership, problem solving, interpersonal skills). Good attention to detail. Methodical approach to work. Good understanding of medical and clinical research terminology and clinical research processes. An understanding of the basics of physiology, pharmacology, and medical devices (when applicable). Good understanding of the principles of ICH GCP, ISO 14155 (if applicable) and local regulatory requirements. Good computer literacy with working knowledge of PCs, Windows and Microsoft Office applications. Good oral and written internal and external communication. Strong interpersonal team and organizational skills, personal presentation. The ability to communicate effectively in English. Focus on Customer. Innovate and Change. Pursue Scientific and Process Excellence. Work with Others. Achieve Results. Ability to maintain confidentiality of data and information during interactions with staff at all levels and across studies and sponsors. Demonstrated ability to conduct clinical operations activities most effectively and efficiently. Good analytical and negotiation skills. Experience using e-clinical systems [e.g., clinical trial management system (CTMS)]. For medical device positions, experience in providing customer service to device end users. Physical Demands/Work Environment Must be able to sit at a computer for long periods of time. Must be able to use hands to finger, handle or touch objects, tools or controls, including a computer keyboard, for up to 8 hours per day. Standard office and/or home working environment. Clinical Research Unit and hospital environment (administrative only). Risk of eye strain. Will involve outside of normal office hours as required by the role. Travel Requirement is 60% of the time (traveling to study sites). Learn more about our EEO & Accommodations request here.

The candidate should possess excellent communication, negotiation, and interpersonal skills, along with a strong understanding of medical terminology, pharmacology, and the healthcare industry. A minimum of two years of relevant experience is required. Job Type: Full-time Pay: ₹25,000.00 - ₹30,000.00 per month Benefits: Cell phone reimbursement Flexible schedule Health insurance Life insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person Application Deadline: 17/07/2025

Dispensing medications, providing medication information, medical center experience ensuring patient safety. They review prescriptions, counsel patients on drug use Managing inventory Ensuring regulatory compliance

The Position Will be responsible for executing medical affairs strategy in the assigned zone. Tasks & Responsibilities Understand the current practices, medicines being used, and trends in relation to their respective therapeutic area through key customer contacts, attending scientific symposia and reviewing key therapeutic journals in order to provide relevant information to internal and external customers. Effectively gathers and disseminates information in a concise and understandable format to both internal and external customers and position BI Medical as a preferred partner for key customers through credible and clear non-promotional communication Execute key medical projects (e.g. IIS studies) to ensure that BI interacts most efficiently with customers and key customer networks through optimal contact, so as to bring significant value to both the customer and BI Participate in the implementation of the local medico marketing strategy. Identify the EEs in the territory. Develop relationship with team and network for effective promotion of BI and BI products. Give feedback to the management regularly about KOL development. Provide medical and product expertise towards registration of new products/indications with federal/state regulatory authorities through delivery of scientific presentations, provision of medical rationale and published literature, and liaison with key HCPs for obtaining support for new product/indication. Provide medical and product expertise towards defense of marketed products (regulators, NGOs, press, etc.) Write, revise, and review labeling documents for pipeline/local products per relevant SOPs. Assist regulatory affairs with EE access when appropriate. Requirements Education : Medical degree (preferable qualification in Pharmacology), or qualification in life-sciences. Preferably 0-3 years experience on the same field and Pharmaceutical or Healthcare industry. Beginner level can apply as long as candidate is graduate of MD of Pharmacology. For professional without doctoral qualification, relevant field-based work experience of 10+ years with good scientific expertise is preferable. Scientific expertise on diabetes therapy area is required. Excellent interpersonal skill. Basic IT Knowledge on MS Office applications Role is based in Delhi READY TO APPLY? Click the “Apply On Company website” button. Create an account or sign in and continue to register your profile, upload your resume, and apply in the company site. For any technical issues or additional questions, contact HR Direct. (Note: resumes should not be submitted to HR Direct since job applications are not processed via email or phone call) HR Direct contact information: Phone: +91-22-7145-6700 Email: HRDirect.PH@boehringer-ingelheim.com Our Company Why Boehringer Ingelheim? With us, you can develop your own path in a company with a culture that knows our differences are our strengths \u2013 and break new ground in the drive to make millions of lives better. Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed. Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after \u2013 as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations. Want to learn more? Visit https://www.boehringer-ingelheim.com

The Position Will be responsible for executing medical affairs strategy in the assigned zone. Tasks & Responsibilities Understand the current practices, medicines being used, and trends in relation to their respective therapeutic area through key customer contacts, attending scientific symposia and reviewing key therapeutic journals in order to provide relevant information to internal and external customers. Effectively gathers and disseminates information in a concise and understandable format to both internal and external customers and position BI Medical as a preferred partner for key customers through credible and clear non-promotional communication Execute key medical projects (e.g. IIS studies) to ensure that BI interacts most efficiently with customers and key customer networks through optimal contact, so as to bring significant value to both the customer and BI Participate in the implementation of the local medico marketing strategy. Identify the EEs in the territory. Develop relationship with team and network for effective promotion of BI and BI products. Give feedback to the management regularly about KOL development. Provide medical and product expertise towards registration of new products/indications with federal/state regulatory authorities through delivery of scientific presentations, provision of medical rationale and published literature, and liaison with key HCPs for obtaining support for new product/indication. Provide medical and product expertise towards defense of marketed products (regulators, NGOs, press, etc.) Write, revise, and review labeling documents for pipeline/local products per relevant SOPs. Assist regulatory affairs with EE access when appropriate. Requirements Education : Medical degree (preferable qualification in Pharmacology), or qualification in life-sciences. Preferably 0-3 years experience on the same field and Pharmaceutical or Healthcare industry. Beginner level can apply as long as candidate is graduate of MD of Pharmacology. For professional without doctoral qualification, relevant field-based work experience of 10+ years with good scientific expertise is preferable. Scientific expertise on diabetes therapy area is required. Excellent interpersonal skill. Basic IT Knowledge on MS Office applications Role is based in Mumbai READY TO APPLY? Click the “Apply On Company website” button. Create an account or sign in and continue to register your profile, upload your resume, and apply in the company site. For any technical issues or additional questions, contact HR Direct. (Note: resumes should not be submitted to HR Direct since job applications are not processed via email or phone call) HR Direct contact information: Phone: +91-22-7145-6700 Email: HRDirect.PH@boehringer-ingelheim.com Our Company Why Boehringer Ingelheim? With us, you can develop your own path in a company with a culture that knows our differences are our strengths \u2013 and break new ground in the drive to make millions of lives better. Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed. Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after \u2013 as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations. Want to learn more? Visit https://www.boehringer-ingelheim.com

Role & responsibilities Clinical trial designing, protocol inputs for generic products and their FDCs The position is to Lead team of scientists to accomplish activities related to clinical trial designing, monitoring, concluding and MMA. Phase trials I IV execution. NDDS product development. Define objectives/ sample size calculation for protocols of clinical trials. AE/ SAE monitoring & reporting. Site selection/ site evaluation. Training to investigators, guide the trial site for execution of the study as per expectation of protocol. Preferred candidate profile MD (Pharmacology) with 2-4 yrs of relevant experience. Interested candidates are requested to share their CVs on vilshashah@torrentpharma.com

Opportunity to spearhead the One Health Initiative Opportunity to join a leading vaccine company in India About Our Client Our client is the market leader in veterinary and human biologicals in India. Job Description The key responsibilities include: Strategic Leadership Develop and execute the R&D strategy aligned with corporate vision and market needs. Lead long-term innovation and product development roadmap. Identify new technologies, partnerships, and platforms to strengthen the R&D pipeline. Scientific Oversight Supervise discovery, preclinical, and/or clinical research programs. Ensure scientific rigor and regulatory compliance across all projects. Drive IP strategy and oversee patent filings in collaboration with legal teams. Team Management Build, mentor, and manage multidisciplinary R&D teams (molecular biology, biochemistry, pharmacology, bioinformatics, etc.). Foster a culture of innovation, collaboration, and accountability. Project and Portfolio Management Oversee project prioritization, resource allocation, timelines, and budgets. Manage internal and external collaborations, including CROs, academic partners, and technology vendors. Regulatory and Quality Interface Coordinate with QA/RA teams to ensure compliance with FDA, EMA, and other global regulatory bodies. Support IND/NDA submissions, clinical trial design, and documentation processes. Cross-Functional Collaboration Collaborate closely with business development, manufacturing, marketing, and clinical operations. Translate R&D outcomes into business value and marketable products. The Successful Applicant The successful candidate would have: Animal health R&D background preferred; if from human health, the ideal candidate must have viral vaccine/ polysaccharide conjugate vaccine experience. Expertise in viral and bacterial vaccines. PhD and ownership of patents/ high-impact publications are desirable. Strong grasp of emerging science trends, solid analytical understanding, and familiarity with the technical aspects of clinical testing. Proven leadership ability What's on Offer The role offers the opportunity to lead large-scale vaccine R&D programs with direct impact on innovation, scientific direction, and product development. Contact: Sangya Shaily Quote job ref: JN-072025-6780858

University: Helmholtz Centre for Infection Research (HZI) Country: Germany Deadline: 2025-07-30 Fields: Chemistry, Biochemistry, Pharmacology, Molecular Biology, Microbiology The Chemical Biology Department at the Helmholtz Centre for Infection Research (HZI), under the leadership of Prof. Brönstrup, is seeking applications for a PhD researcher in the field of Bioanalytical Chemistry / Metabolomics. HZI is a member of the Helmholtz Association of German Research Centres, the largest scientific organization in Germany, and is dedicated to advancing strategies for the prevention, diagnosis, and treatment of infectious diseases. Research at HZI focuses on both bacterial and viral pathogens, their interactions with the immune system, and the discovery of novel therapeutic compounds. The Chemical Biology Department is committed to the discovery and characterization of new anti-infective agents through screening, mode of action studies, and chemical synthesis. Requirements For Application – Cover letter outlining your motivation and suitability for the position – Curriculum vitae (resume) – Employment references and certificates – Work samples or reference projects (if available) – Please do not include a photograph Application Procedure Applicants should submit all required documents, quoting the reference number 076/2025, to the Human Resources Department, Helmholtz Centre for Infection Research GmbH, Inhoffenstr. 7, 38124 Braunschweig, Germany. Applications may also be submitted by email as a single PDF document to jobshzi@helmholtz-hzi.de. Further information about the position can be found at: https://www.helmholtz-hzi.de/en/career/job-portal/job/076-2025-phd-researcher-f-m-d-in-bioanalytical-chemistry-metabolomics/ Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/position-alert-service/ We’re an independent team helping students find opportunities. Found this opportunity helpful? Support us with a coffee! Also See Postdoctoral Position in Chrononutrition at the German Institute of Human Nutrition Graduate Teaching & Research Assistant Position in Medicinal Chemistry and/or Chemical Biology Doctoral Scholarship in Immunoparasitology and Vaccine Development PhD Opportunities in Plastic Pollution and Climate Sustainability PhD Position in Gut Microbiota, Immune Regulation, and Liver Health in Diabetes

Job Title: Senior Pharmacist Company Name: Manipal Hospitals Job Description: As a Senior Pharmacist at Manipal Hospitals, you will play a critical role in delivering high-quality pharmaceutical care to patients. You will be responsible for managing the pharmacy department, overseeing medication distribution, ensuring compliance with healthcare regulations, and providing expert medication counseling to healthcare professionals and patients. Your role will involve collaborating closely with interdisciplinary teams to optimize therapeutic outcomes and enhance patient safety. Key Responsibilities: - Oversee the daily operations of the pharmacy department, including medication preparation, dispensing, and inventory management. - Ensure compliance with all legal, regulatory, and accreditation requirements related to pharmacy operations. - Provide clinical pharmacy services including medication therapy management, drug utilization review, and formulary management. - Assist in the training and mentoring of junior pharmacists and pharmacy staff. - Evaluate and verify medication orders for accuracy, appropriateness, and safety. - Educate healthcare professionals and patients about medication therapies, including proper administration and potential side effects. - Conduct medication reconciliation to ensure continuity of care for patients. - Participate in quality improvement initiatives and contribute to patient safety programs. - Stay updated with the latest developments in pharmacy practice, pharmacotherapy, and drug information. Skills Required: - Strong knowledge of pharmacology, therapeutics, and pharmacy regulations. - Excellent clinical judgment and decision-making abilities. - Good communication and interpersonal skills for effective patient and team interaction. - Strong organizational skills with the ability to prioritize tasks effectively. - Proficiency in using pharmacy management software and electronic health records (EHR). - Adept at conducting clinical assessments and evaluating patient medication regimens. - Commitment to continuous learning and professional development. Tools Required: - Pharmacy management systems (e.g., Pyxis, Meditech). - Electronic health records (EHR) systems. - Drug information databases (e.g., Micromedex, Lexicomp). - Medication therapy management software. - Inventory management tools and software. - Standard office software (e.g., Microsoft Office Suite). This position requires a dynamic individual with a strong commitment to patient care and a collaborative approach to healthcare. Join us at Manipal Hospitals and be part of a team dedicated to providing exceptional pharmaceutical services. Roles and Responsibilities About the Role: As a Senior Pharmacist at Manipal Hospitals, you will play a vital role in ensuring optimal medication management for patients. You will be responsible for overseeing pharmacy operations, ensuring compliance with regulatory standards, and providing expert guidance on pharmacotherapy to healthcare providers. You will also participate in clinical rounds and collaborate with multidisciplinary teams to enhance patient care. About the Team: You will be part of a dynamic and collaborative team that includes fellow pharmacists, pharmacy technicians, and healthcare professionals committed to patient safety and medication efficacy. The team values continuous learning and innovation, working together to improve pharmaceutical care services across the hospital. A supportive work environment fosters professional development and knowledge sharing. You are Responsible for: - Managing medication therapy and ensuring the safe dispensing of pharmaceuticals. - Conducting medication reconciliation and providing consultations to healthcare providers. - Developing and implementing pharmacy policies and procedures to enhance service delivery. - Supervising pharmacy staff and ensuring their adherence to best practices. - Monitoring drug utilization patterns and conducting quality improvement initiatives. To succeed in this role – you should have the following: - A Bachelor’s or Doctor of Pharmacy (PharmD) degree from an accredited institution. - Valid pharmacy license and relevant clinical experience in a hospital setting. - Strong knowledge of pharmacology, therapeutics, and medication management. - Excellent communication and interpersonal skills to work effectively with multidisciplinary teams. - A commitment to continuous professional development and staying updated on pharmaceutical advancements.