1113 Pharmacology Jobs - Page 37

Ascentrik Research Pvt. Ltd is a premier Research & Data Service Provider serving the Top Fortune 500 Companies & many more Multi-National Companies across different industries & sectors. We are pioneers in customized Research Services and are providing actionable insights with quality data to our clients. We are operating with a large work force from offices in Pune, Navi Mumbai and Noida and are aiming to grow even more. We are looking out for a Sr. Clinical Research professional who has a relevant experience and has excellent knowledge. Beacon Targeted Therapies (https://beacon-intelligence.com/) Beacon provides a customizable, modular, cloud-based software-as-a-service platform that enables you to personalize drug development data and analysis so that it seamlessly integrates into your daily workflows. The solutions are designed to enable multinational pharma, biotech and anyone with a vested interest in the progress and development of new therapies to conduct: Target discovery and analysis Candidate screening and benchmarking Market entry and exit strategy Trial design and development Translational science analysis Key Responsibilities Lead and manage a research team in order to curate accurate, timely, insightful and comprehensive data and intelligence. Identify and analyse the most relevant information for Beacon and its users. Coordinate with UK based clients on a regular basis to understand and meet the project deliverables. Manage the activities required towards launch of a beacon module and further support the needs towards maintenance post launch. You will be part of a global network of life science researchers working on dynamic, fast growing products in exciting, cutting edge life science areas. Perform data management activities on the assigned project in a timely and efficient manner Generate queries to clarify and improve the quality of the data. Strong understanding of Clinical Trials and their data Strong understanding on preclinical data What attributes will you need? An ideal candidate might be a subject matter expertise in various drug therapies in field of oncology (Antibody drug conjugate/Bispecific/Adoptive cell therapy/Checkpoint modulators/oncolytic virus/Gene therapy) and experience with managing a team of resources. Proven ability to deal with complex life science concepts Excellent written and verbal communication skills. Previous experience in a research role and/or data-oriented role is desirable but not essential. Experience and understanding in the field of pharmacology, drug discovery and development and clinical trials would be a bonus. Good project and people management skills are a must have. Results-oriented, passionate about delivering value and impact, proactive. Most of all, you will need to be curious and willing to learn at all times. Eligibility Masters in Pharmacy (except Pharmacognosy)/Biology/Bio-Technology/Bio-Chemistry/Pharm D with minimum 2-3+ years’ of relevant experience Bachelors in Pharmacy (except Pharmacognosy)/Biology/Bio-Technology/Bio-Chemistry with at-least 4 years of relevant experience Candidates with additional Clinical research diploma or relevant courses can apply. Candidate should have basic computer skills, Microsoft Office & detailed Internet Knowledge. Candidate should have one research paper published Ability to work in a high-pressure, deadline-driven environment Exceptional communication and reporting skills Location Pune, Maharashtra Apply Now To apply please email your CV to hr@ascentrik.com

JOB_DESCRIPTION.SHARE.HTML CAROUSEL_PARAGRAPH JOB_DESCRIPTION.SHARE.HTML India - Bengaluru Medical & Safety No Regular Full-Time 2524 Emmes Global mail_outline Get future jobs matching this search or Overview Job Description Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose The Safety Monitor II will implement Pharmacovigilance activities in collaboration with other members of the Pharmacovigilance and Medical Monitoring (PMM) department, under general supervision. The Safety Monitor II will assist senior level Safety Monitors with interventional and non-interventional clinical projects in conjunction with the assigned Medical Monitor/Medical Officer and the project team and may be assigned as the Primary Safety Monitor for small projects. In addition, the Safety Monitor II will assist with the designing and execution of the assigned Pharmacovigilance (PV) related projects (e.g., management of local or international PV systems for contracted Clients; PV supervision of RWE (Real World Evidence projects); etc.) in close cooperation with other Emmes roles, especially with Medical Officers/Medical Monitors (or other similar medical expert roles), Regulatory roles, etc. The Safety Monitor II will support the adherence to Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP) and other relevant Pharmacovigilance requirements. Responsibilities Assists in performing safety monitoring activities in cooperation with project Medical Monitor/Medical Officer and other relevant project team members. Reviews safety events. Assists in the collection, assessment, monitoring, review and reporting of adverse drug reaction cases from all sources – clinical (both interventional and non-interventional), data sets analyzed in association with RWE projects, spontaneous reports, literature, etc. ▪ Provides first line evaluation of serious adverse events (SAEs). Communicates with site staff regarding reported AEs or SAEs to gather additional information. Prepares a summary narrative for each reported SAE suitable for Medical Monitor/Officer review, and inclusion in Data Safety Monitoring Board (DSMB) reports, regulatory submissions, and final study reports. Coordinates the timely completion and submission of required reports to health authorities and business partners. ▪ Maintains ongoing database of SAEs and reconciles SAEs in the database as needed. Reviews adverse events and/or other safety related data such as toxicities, concomitant medications and medical history, etc. for the study on a regular basis. Establishes direct communication with Client, investigator site staff, national and regional regulatory authorities, health professionals, pharmaceutical and other study partners, as necessary. Responds to site, Client, DSMB, or Medical Monitor/Officer requests for information regarding safety in clinical trials (both interventional and noninterventional). Participates in DSMB or other safety review committee (SRC) meetings, including Protocol Safety Review Team (PSRT) meetings, as necessary. Reviews and contributes to DSMB/SRC reports regarding safety; reviews and contributes to safety sections of annual as well as periodic safety reports. Coordinates with project staff. Participates in project team meetings for the planning, preparation, and development of all safety-related sections of protocols, study specific safety documents such as Safety Management Plan (SaMP), Manual of Operations (MOP), project Standard Operating Procedures (SOPs), and ancillary documents to ensure project compliance with corporate SOPs. Contributes to the development and implementation of safety-related Case Report Forms (CRF) and SaMP. Ensures maintenance of documentation required by both corporate and project SOPs. Participates in project process improvement and corporate quality assurance activities through Internal Quality Audit Team (IQAT) processes, project SOP and Compliance/Variance table development, participation in both internal and external audits, as well as professional development activities. Performs Medical Dictionary for Regulatory Activities (MedDRA) and World Health Organization (WHO) Drug coding, as applicable. Guarantees compliance and adherence to the quality standards. Contributes to the development and maintenance of departmental quality documents (e.g., SOPs) and other work practices as assigned. Maintains accurate reporting to relevant authorities, such as Food and Drug Administration (FDA), European Medicines Agency (EMA) etc. when applicable per client contract. Contributes to the verification that Quality Control processes are conducted in accordance with applicable written procedures. Completes all relevant professional training in the given scope and time frame. Participates in corporate activities such as corporate safety meetings/activities; annual SOP reviews; cross-department working groups dedicated to improvement of the work processes and development of innovative solutions and other relevant corporate initiatives. Performs other duties as assigned. Qualifications Bachelor’s degree in pharmacology, nursing or other scientific discipline is required with relevant experience in clinical practice (e.g., pharmacy, inpatient or outpatient healthcare facility, or clinical research center, etc.). At least 2 years of related experience in research or with a pharmaceutical company (CRO, SMO, pharma company, etc.) Experience in safety monitoring/pharmacovigilance is preferred. The readiness to work in a regulated environment and understanding of the Good “x” Practice (GxP) principles. Ability to learn and understand quickly. Consistency, quality, compliance and patient centricity respected as key values. Excellent clinical judgement and ability to communicate moderately complex clinical issues in a scientifically sound and understandable way. Detail-oriented with good organizational skills Ability to work as a team member and function on a cross-functional team. Excellent verbal and written communication skills. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes Show more Show less

About Company ASG Eye Hospitals is a chain of super specialty eye hospitals in India. It offers a comprehensive range of eye care services including treatment and surgeries of Retina, Cataract, Squint, Oculoplasty, Cornea, Lasik, ICL, Glaucoma, and Paediatric Ophthalmology. Currently, the group has 165+ Eye Hospitals across 83+ cities in India. Role - Executive - Pharmacist Location - Varanasi,UP Job Responsibilities Provide advice about health issues, symptoms and medications in response to customer enquiries. Process prescriptions and dispense correct medication. Ordering, selling and controlling medicines and other stock. Manage inventory to ensure an adequate supply of medications. Managing budgets Keeping statistical and financial records Preparing publicity materials and displays Counsel patients on proper medication and side effects. Desired Candidate Profile D.Pharm / B.Pharm Must be a registered Pharmacist from the State Pharmacy Council. Good Communication Skills. Must have Basic computer knowledge. Perks and Benefits + Performance Based Incentives Interested candidates mail your resume along with below details on WhatsApp 8875029935 Total Experience - Current City- Home Town- Current CTC - Expected CTC - Notice Period -

Assistant Professor Pharmacology Associate Professor Pharmacology Professor for Pharmacology 9451802744 9415408154

A pharmacologist investigates how drugs and other chemical substances interact with living organisms, including humans and animals. They conduct research to understand drug effects, develop new medications, and ensure the safe use of existing drugs.

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Read and understand analytical procedures Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs Gain a technical understanding of the techniques in which review is being performed Use MS Windows applications such as EXCEL, Word, Access, Outlook email Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications M.Pharm (Pharmaceutical Analysis) / M.Sc Chemistry Additional Information Experience level : 0 - 2 years in Bio/Pharmaceutical Analysis Key Candidate Attributes: Self-motivation; excellent quality of work and attention to detail Ability to communicate effectively with coworkers and internal/external clients Ability to learn new tasks quickly and to move easily from task to task Ability to handle prioritization and multiple tasks simultaneously Ability to use a personal computer and learn necessary programs Good communication skills (oral and written) Organizational ability and good judgement Science background/education and/or laboratory experience

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. The Project Manager Assistant (PMA) position is an administrative role working directly with a group of Project Managers, focusing on a specific area of the business. This role requires the use of technical functions to navigate Eurofins Lancaster Labs (ELLI) information systems, construct and develop relationships with ELLIs internal scientific and support departments, and assist project managers with a variety of tasks to allow the PMs to focus on client communication. Please note that this position does require direct client interaction. This is a great role if you also aspire to move into a PM position in the future. Employee Responsibilities: Support Sample and Project Management in building and maintaining studies including entering and review of material items, study start and end dates, and generating project plans for the PM teams. Managing incoming and in house Reference Standards by reaching out to the client for updated CoAs when expirations are approaching. Working with Pricing and Analytical Definition to generate quotes and build templates for sample entry of incoming samples. Track financial aspects of projects including purchase order and invoice management. This may also include generating Change Orders, special invoice requests and potentially End of Month billing for clients that qualify. Support Project Managers in an administrative capacity with a variety of other assignments Qualifications M. Pharm / M.Sc, Analyitical Chemistry PMP certification would be an additional advantage Additional Information Experience Level : 5 - 7 years in Bio/Pharmaceutical Analysis Key Candidate Attributes: Possesses excellent communication skills both oral and written Has a strong organization and attention to detail Computer skills Experience utilizing MS Office and MS Project or other project organization tools. Experience navigating a LIMS or equivalent is a plus Ability to learn new techniques, perform and prioritize multiple tasks simultaneously, keep accurate records, follow instructions, and comply with agency and company policies (GMP knowledge is a plus) Ability to work both independently and as part of a team, be self-motivated, adaptable, and maintain a positive attitude, even with critical deadlines Initiative/ Self-Starter proactively seek out work and training opportunities, offer to assist others, strive for high productivity and output in a fast-paced environment

Hi, We are hiring for the Leading ITES Company for Medical Writing Role. Job Description: Prepare and review clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, and Post Approval Documents across the Therapeutic Areas. Quality check of the clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, Clinical Summary of Safety, Clinical Summary of Efficacy and Common Technical Document Modules. Initiate start up meetings with the Study Teams related to the creation and development of the clinical document for regulatory submission, if required. To work in coordination with all the members in the study team- internal and external for the development of clinical documents. Share project timelines amongst the study team for the development of document. Prepare Clinical Documents according to the Standard Operating Procedures, Document Standards and Guidance document. Review statistical analysis plans and table/figure/listing, when required. Ensure uniformity and consistency in the scientific content of the regulatory documents Preparation of documents in the scope and other Medical Writing documents that may be required for domestic and international regulatory submissions to the US, European, and other regulatory agencies Prepare Medical Writing documents within established timelines that are of high quality for scientific content, organization, clarity, accuracy, format, and consistency, with adherence to regulatory guidelines and applicable standards, styles, guidelines, and processes. Perform peer review and quality control review of the documents within established timelines with adherence to applicable guidelines, and processes, using appropriate checklists. Take an active role on assigned projects with respect to planning of content, format, and timing of documents, report scheduling/tracking, etc. Provide support to the assigned clinical development or project team to ensure that project needs, and department standards are met, while completing reports within established schedules/timelines. Plan and organize project and non-project meetings, as and when required Key Skills: a) Min 1 Year Experience in Clinical Study and Summary Writing Common Technical Document. b) Should have Experience in making Clinical Study Pharmacology Report, Clinical Study Report and Clinical Summary of Safety c) Any Graduate To Apply, WhatsApp 'Hi' @ 9151555419 Follow the Steps Below: >Click on Start option to Apply and fill the details >Select the location as Other ( to get multiple location option ) a) To Apply for above Job Role ( Bangalore ) Type : Job Code # 396

Hi We are hiring for ITES Company Role -Medical Reviewer Qualification : MBBS/MD only (MCI Certification is not mandate**) Experience Range : 1 to 7 Years Preferred Experience: Minimum of 1 years of experience in PV/ Clinical Research (drug safety) Job Description: Author a company clinical comment (CCC) for case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Edit the Periodic Report Comment, if applicable, directly within the Periodic Report Comment field in the Patient Safety database. Perform the following actions within the Comments field of the GSP Review Workflow step in the Patient Safety database: -Review and respond to any queries/comments from the Case Owner, which are recorded in the Comment field of the GSP Review Workflow step in the Patient Safety database. -Detail any requests for changes to the case, including the narrative. -Detail any follow-up information that is required and not already noted within the Query Manager in the Patient Safety database. Provide product advice as required, especially with regards to case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Review the company causality assessment provided by Medical Advisor. • Review the medical sense including seriousness and coding of the case in the global context of the drug or clinical project, including the narrative, AE/SAE terms, suspect drugs, concomitant medications, laboratory data, and medical history. To provide documentation of the review and case comments in Sapphire in Medical Review workflow. Maintain knowledge of the marketed drug currently under litigation. Maintain knowledge of the company disease and therapeutic areas for marketed drugs and drugs in development through periodic medical review training held by client medical staff. Skills required: Computer Literate (good knowledge of MS Office) Sound understanding of the Drug Safety and Regulatory process Good problem solving and decision-making skills Capability to lead by motivation and example Ability to prioritize schedule and organize Excellent interpersonal and communication skills To Apply, WhatsApp 'Hi' @ 9151555419 Follow the Steps Below: >Click on Start option to Apply and fill the details >Select the location as Other ( to get multiple location option ) a) To Apply for above Job Role ( Mumbai ) Type : Job Code # 47 b) To Apply for above Job Role ( Pune ) Type : Job Code # 48 c) To Apply for above Job Role ( Bangalore ) Type : Job Code # 51

Hi We are hiring for the leading ITES Company for the Medical Reviewer Role. Qualification - MBBS/MD is Must (Full TIme) Job Overview: The Medical Reviewer is responsible for the evaluation and analysis of clinical data to ensure accuracy, compliance with regulations, and the highest quality standards. This role involves reviewing clinical trial data, medical documentation, and regulatory submissions to support the approval of new medical products and therapies. Key Responsibilities: Clinical Data Review : Evaluate clinical trial data for completeness, accuracy, and adherence to protocols. Ensure data integrity and consistency across various documents and databases Medical Documentation: Review and verify the accuracy of medical documentation, including patient records, case reports, and clinical study reports. Ensure documentation complies with regulatory requirements and company standards. Regulatory Compliance: Stay updated with the latest regulatory guidelines and ensure all reviews align with current regulations. Prepare and review regulatory submissions to ensure timely and successful product approvals. Training and Development: Stay informed about advancements in medical research and regulatory changes. Participate in continuous training and development programs to enhance knowledge and skills. Skills required: Computer Literate (good knowledge of MS Office) Sound understanding of the Drug Safety and Regulatory process Good problem solving and decision-making skills Capability to lead by motivation and example Ability to prioritize schedule and organize Excellent interpersonal and communication skills To Apply, WhatsApp 'Hi' @ 9151555419 Follow the Steps Below: >Click on Start option to Apply and fill the details >Select the location as Other ( to get multiple location option ) a) To Apply for above Job Role ( Pune ) Type : Job Code # 48 b) To Apply for above Job Role ( Chennai ) Type : Job Code # 52 c) To Apply for above Job Role ( Indore ) Type : Job Code # 53

Continental Hospitals, Gachibowli, Hyderabad Continental Hospital is a JCI and NABH accredited facility offering multi-specialty, tertiary, and quaternary care services with more than 56 specialties, the healthcare institution is spread across 18 floors (1.4 million sq. ft), located in the IT and Financial District of Hyderabad, Gachibowli. Continental Hospitals was founded by Dr Guru N Reddy in April 2013 to redefine healthcare in India by providing quality patient care with integrity, transparency, a collaborative approach, and evidence-based medicine Continental Hospitals, India’s first LEED qualified super specialty hospital is built on international standards and is designed to enhance the healing spaces with natural ventilation, safety, and privacy. The hospital has incorporated the safest standards in the world including fire, water resources, sanitation, and internal transportation systems. Continental Hospitals has a special health check lounge and a dedicated area for international patients, state-of-the-art facilities and medical equipment, as well as the latest communication and information technology. Key specialties include Gastroenterology, Oncology, Orthopedics, Neuroscience, Cardiology, and Multi-organ Transplants. Our proactive team of highly experienced doctors, nurses, and staff ensures that we deliver the highest standard of personalized care to our patients at all times. Job Title: Clinical Pharmacist Department: Clinical Pharmacy Services / Pharmacy & Therapeutics Location: Continental Hospitals, Financial Distt, Nanakramguda Role Summary: We are seeking an experienced and highly competent Clinical Pharmacologist with a minimum of 8 years of proven experience in a multispecialty hospital environment. The ideal candidate will play a key role in ensuring safe, effective, and evidence-based medication use, supporting patient care through clinical expertise and active collaboration with the medical team. Key Responsibilities: Medication Safety: Implement and monitor medication safety protocols to reduce errors and enhance patient safety. Medication Reconciliation: Conduct thorough medication reconciliation during patient admission, transfer, and discharge to avoid discrepancies. Medication Therapy Management (MTM): Evaluate and optimize medication regimens in collaboration with physicians to ensure therapeutic effectiveness and minimize risks. Adverse Drug Event (ADE) Reporting: Identify, document, and report adverse drug reactions and medication errors per hospital and regulatory protocols. Medication Management: Oversee appropriate storage, usage, and administration of drugs across clinical departments in compliance with regulatory guidelines. Therapeutic Drug Monitoring: Monitor and adjust dosages for high-risk medications (e.g., antibiotics, anticoagulants) based on pharmacokinetic and lab data. Prescription Auditing: Audit prescriptions for accuracy, appropriateness, interactions, and compliance with hospital formulary and guidelines. Drug Dose Calculations: Ensure correct dosage calculations, especially for pediatric, geriatric, renal, and critical care patients. Protocol Development: Participate in the development and review of drug use protocols, clinical pathways, and standard treatment guidelines. Case & Seminar Presentations: Prepare and deliver case studies, clinical reviews, and seminars to enhance pharmacy and interdisciplinary knowledge. Required Qualifications & Experience: Education: M. Pharm / Pharm. D (Doctor of Pharmacy) Experience: Minimum 8 years of experience in a clinical pharmacy role within a multispecialty hospital Licensure: Registered with State Pharmacy Council Key Competencies: In-depth knowledge of pharmacology, clinical therapeutics, and drug interactions Strong analytical and problem-solving skills Excellent communication and presentation abilities Commitment to patient-centered care and interdepartmental collaboration Familiarity with EMR systems and pharmacy informatics tools Preferred Certifications: Certification in Clinical Pharmacy Practice / Pharmacovigilance Advanced training in MTM or Medication Safety (preferred) Show more Show less

Job Description Designation: Subject Matter Expert (SME) – Pharmacy Employment: Full Time Location: Hyderabad, India Job Summary: We are looking for a dedicated and detail-oriented Subject Matter Expert (SME) in Pharmacy to join our academic content team in Hyderabad. The SME will be responsible for developing, reviewing, and ensuring the accuracy and quality of pharmacy-related academic content in alignment with current curriculum and industry standards. Key Responsibilities: · Develop and structure academic content for Diploma, B.Pharm courses, including study material, assessments, case studies, MCQs, and digital learning modules. · Ensure all content is scientifically accurate, pedagogically effective, and aligned with pharmacy regulatory bodies (e.g., PCI, AICTE, UGC). · Collaborate with instructional designers, editors, and multimedia teams to create engaging and interactive e-learning content. · Review and validate existing content created by internal teams or external contributors for accuracy, consistency, and curriculum alignment. · Research and incorporate the latest developments in the field of pharmacy, including pharmacology, pharmaceutics, pharmacognosy, and pharmaceutical chemistry. · Provide academic expertise in planning curriculum structures and designing learning outcomes. · Train and mentor junior writers, freelancers, or interns, if applicable. · Participate in academic audits, feedback implementation, and content improvement strategies. Required Qualifications & Skills: Master’s degree in Pharmacy (M.Pharm) from a recognized institution. Minimum 1+ years of experience in academia, clinical research, pharmaceutical industry, or content development. Strong foundational knowledge in core pharmacy subjects such as Pharmacology, Pharmaceutical Analysis, Pharmaceutics, and Medicinal Chemistry. Familiarity with academic frameworks like Bloom’s Taxonomy, outcome-based education (OBE), etc. Proficiency in MS Office Suite (Word, Excel, PowerPoint); experience with LMS or content tools (Articulate, Moodle) is a plus. Ability to work independently with attention to detail and accuracy. Job Types: Full-time, Permanent Pay: ₹28,000.00 - ₹35,000.00 per month Benefits: Commuter assistance Provident Fund Schedule: Day shift Work Location: In person

Work Schedule Standard (Mon-Fri) Environmental Conditions Office At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Discover Impactful Work: We are passionate about being data and technically agile and driving enhanced value for our clients and patients. Determined to improve patient health, we help PPD provide industry-leading statistical, programming and clinical pharmacology contributions through global delivery, consistent quality adherence and scientific insight. A day in the Life: Administers the daily financial management of simple or moderately complex studies, for the functional area's portion of a project budget, as assigned with minimal supervision. Performs review of contract and bidding assumptions. Performs analysis of budget to actual data on monthly or other specified basis. Works closely with project lead to update resource forecasts and unit grids, present and resolve pending issues with resource forecasts, unit grids and contract modifications. Close collaboration with other departments and project lead to coordinate financial aspects of functional area's portion of projects. Assists project team to identify risks, define reasons for unsupported hours, and attends risk meetings as needed. Prepares estimates for contract modifications. Keys to Success: Education Bachelor's degree in finance, accounting, mathematics or related field or equivalent and relevant formal academic / vocational qualification, and Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). The following education and experience is preferred: Experience 2+ years complex project management experience to include allocation of resources against budget, forecasting, and completion/coordination of related quantitative and analytical tasks Knowledge, Skills, Abilities Shown budgeting and forecasting skills Solid analytical skills and capable of handling data effectively Solid problem solving skills Good written and verbal communication skills Strong digital literacy (Microsoft Office, etc.) for analysis and presentation of data Good understanding of project management principles and application Capable of focusing on individual projects while covering similar aspects across multiple projects Capable of working independently Capable of providing mentorship and promoting partnership in a multi-disciplinary team setting Solid organizational skills with the ability to adapt and adjust to changing priorities Positive attitude Show more Show less

Bachelor’s degree in pharmacy or pharmacology is not mandatory Proven experience as a pharmacist or any medical shop Detailed understanding and knowledge of dosage requirements and administration, chemical compounds, and pharmaceutical brands. Working knowledge of Microsoft Office Suite and software applications, used by pharmacies, such as MEDITECH and Mediware. Great organizational skills. Excellent verbal and written communication skills. Job Types: Full-time, Permanent Pay: ₹10,000.00 - ₹14,000.00 per month Benefits: Cell phone reimbursement Paid sick time Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Application Question(s): Are you comfortable with Dunlop location? How many years do you have experience as a pharmacist? fresher is not applicable Work Location: In person

We are looking for an MSL- Oncology for a Global Pharmaceutical MNC Profile: Medical Science Liaison- Oncology Location: Delhi/ Kolkata/ Chennai (3 openings) Qualification: MD Pharmacology fresher or with minimum 6 months of experience MDS/ PhD with minimum 1yr of Oncology experience as MSL/RMA Job Purpose: The Medical Science Liaison (MSL) will establish the company’s medical affairs presence with external stakeholders through scientific exchange and research support in oncology. The focus will be on licensed and non-licensed products for hard-to-treat cancers, including metastatic pancreatic cancer, cholangiocarcinoma, digestive cancers (such as stomach cancer, pancreatic cancer, and cholangiocarcinoma), glioma, brain tumors, hematologic cancers (acute myeloid leukemia, acute lymphoblastic leukemia, and lymphoma), and pediatric cancers. This role is field-based, covering the India region. The MSL will communicate balanced therapeutic area-related, product-related, and clinical information to external stakeholders (e.g., physicians, academic institutions, hospital formulary committees), respond to unsolicited requests for medical information, facilitate research discussions, and bring key insights from the medical and scientific community to internal stakeholders. The role also involves ensuring compliance with all company procedures, confidentiality standards, and contributing to business success with a focus on patient safety. Principal Accountabilities: 1. Exchange of Medical and Scientific Information: Responsible for communicating fair and balanced therapeutic area-related, product-related, and clinical information to external stakeholders. Execute the scientific engagement plan in alignment with the Therapy Medical Plan. Proactively develop long-term peer-to-peer relationships with opinion leaders and relevant stakeholders. Respond to unsolicited requests for medical information, including off-label data, related to marketed products and pipeline products. Provide clinical and medical presentations to external stakeholders as needed. Disseminate updates from scientific meetings and report information of strategic interest to cross-functional teams. 2. Supporting Clinical Research: Support ongoing and future Medical Affairs Company-Sponsored Studies, providing country-level review of proposed research site lists, attending site visits if necessary, and providing feedback to the line manager. Support unsolicited requests for investigator-initiated trials (IITs) proposals by offering appropriate investigator support as per company SOPs. Assist in the development and support of national disease registries and Real-World Evidence (RWE) projects as necessary. 3. Contributing to the Organization through Medical Expertise & Market Insights: Maintain up-to-date knowledge of scientific/medical developments in the relevant therapeutic area through literature searches, clinical papers, conferences, and other relevant events. Capture and share in-field insights to develop territorial Field Medical Plans and support medical and scientific strategies. Provide medical and scientific expertise to commercial partners within regulatory guidelines. Act as a field-based scientific and clinical reference for internal stakeholders (e.g., sales, market access) through training and ad-hoc support. 4. Cross-Functional Collaboration: Support the development of medical/scientific materials, ensuring content is reviewed and approved according to company policies. Contribute to the development and execution of the regional medical affairs strategy and action plan in collaboration with field departments such as Sales, Clinical Research, and Market Access. Keep medical representatives and their managers informed about the latest scientific developments. Support the market access strategy at a regional level, including hospital listings, in coordination with the market access manager. 5. Compliance with External Regulations and Company Policies: Maintain a high level of scientific, clinical, and environmental knowledge through courses, self-learning, and attendance at relevant meetings. Stay informed about regulations related to medical information services in the pharmaceutical industry. Ensure all activities comply with internal and external codes of conduct, prioritizing patient safety by following pharmacovigilance processes. Support the company’s reputation in the field by adhering to industry regulations. 6. Patient-In Activities: Support patient awareness initiatives, both physical and digital. Contribute to the Patient-In strategy, understanding the patient journey in coordination with therapeutic area experts, and set up Patient Support Programs (PSPs) to improve patient outcomes as per local regulations. General Administration: Complete all required administration within the specified timelines. Submit monthly reports and expenses by the second working day of each month. Ensure timely completion and submission of all required documentation to the Head Office as appropriate. Profile Requirements A] Minimum Requirements: Education: MBBS/MD Minimum 1-2 years of working experience in oncology. B] Indispensable Qualities: Strong ability to learn new subjects and environments comprehensively. Excellent written and spoken communication and presentation skills, with the ability to build and maintain collaborative relationships with opinion leaders, physicians, and other healthcare decision-makers. Substantial business acumen and autonomy in managing priorities and activities. Strong commitment to compliance with relevant rules and procedures, as well as scientific integrity and quality. Ability to manage cross-functional projects effectively. Leadership skills, emotional intelligence, active listening, and strength of conviction. Negotiation and problem-solving abilities. Proficiency in English is essential. Ability to innovate and execute strategies effectively. Relevant candidates can share their CV at pooja.j@domniclewis.com Show more Show less

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

🔹 Job Title: Freelance Subject Matter Expert (SME) – Pharmacy Subjects 📍 Employment Type: Freelancer 🌐 Location: Work From Home 📢 Open Positions (Subject-wise): Pharmacology Pharmaceutical Chemistry Pharmacognosy Pharmaceutics Allied Subjects (Biochemistry, HAP, Biotechnology, etc.) 🎓 Qualification & Eligibility: Must hold or be in the final year of a B.Pharm degree. Strong command over the selected subject area. 🧠 Experience: 0 to 1 year of relevant experience. Freshers with good knowledge are welcome. 💼 Skill Set Requirements: Basic understanding of Google Suite (Docs, Sheets, Drive, etc.) Clear understanding of quality standards in academic question creation. Must have appeared for Pharmacy entrance/competitive exams like GPAT, NIPER, Drug Inspector, etc. 📌 Roles & Responsibilities: Create high-quality, original, and exam-relevant MCQs and questions for: GPAT NIPER Drug Inspector Exams Ensure academic accuracy, clarity, and relevance of content. Follow the prescribed format and quality benchmarks. 💻 Work Mode: Remote/Freelance – flexible working hours. If you are passionate about pharmacy education and want to contribute to helping aspirants succeed, apply now! Show more Show less

We Are Hiring - International Sales Specialist – Life Sciences Online Education Experience: Minimum 6 to 8 Years Industry: Education / E-Learning / EdTech Joining: Immediate Joiners Preferred Company: YesM Pharma Job Description: We are a US-based online education provider offering specialized courses in Life Sciences, including Pharmacology, Pharmacokinetics & Pharmacodynamics, Signal Detection, Clinevo database training, and Clinical Trial Management. We are looking for a results-driven International Sales Specialist to promote our courses to foreign medical doctors and healthcare professionals. The ideal candidate should have a solid background in international education or healthcare sales, with an understanding of life sciences or medical training. Key Responsibilities: Drive international sales for online Life Sciences training programs Generate leads, pitch services, and convert prospects across the USA, UK, and Middle East markets Conduct virtual presentations and follow-ups with individual Build and maintain long-term relationships with foreign medical professionals and clients Maintain CRM and sales reporting tools with updated pipeline and progress Coordinate with academic and marketing teams for campaign execution Desired Candidate Profile: 6–8 years of international sales experience (preferably in education, training, or healthcare industry) Strong exposure to USA, UK, and Middle East markets Excellent English communication skills (spoken and written) – must be able to engage fluently with foreign clients Background in Life Sciences, Pharmacy, or Medical domain is a strong advantage Familiar with CRM tools and remote sales practices Must be comfortable working USA shift hours Only candidates with relevant international B2B/B2C sales experience will be considered. Mail CV - pankaj@marketingpanthers.com Show more Show less

Pharmacist (Immediate Joiners) Walk-in Interview : Time : 12 pm Location:- Nashik / D. Vijay Pharma Pvt. Ltd. Old, Mumbai - Agra National Hwy, next to Samrat Hotel CBS, Nashik, Maharashtra 422001 Designation: Pharmacist Gender: Male Work Experience: 0-4 Years in Retail / Hospital Attached Medical Store Job Description: Dispensing prescribed drugs as per physicians instructions / hospital’s indent. As a Jr. 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 Salary : 12000 to 20000 (per month) Job Types: Full-time, Permanent, Fresher Pay: ₹12,000.00 - ₹20,000.00 per month Benefits: Cell phone reimbursement Health insurance Leave encashment Life insurance Paid time off Provident Fund Schedule: Day shift Evening shift Morning shift Rotational shift Supplemental Pay: Overtime pay Performance bonus Shift allowance Yearly bonus Education: Diploma (Required) Experience: Total: 1 year (Required) License/Certification: Pharmacist License (Required) Location: Nashik, Maharashtra (Required) Shift availability: Day Shift (Required) Night Shift (Required) Overnight Shift (Preferred) Work Location: In person

Job Description You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise. Officer - Store Company: Ahlcon Parenterals IN Ltd Job Posting Location: IN-Bhiwadi Functional Area: Supply Chain Management Working Model: Onsite Requisition ID: 4929 Are you a Store Officer passionate about Physical verificationa, dispensing and documentation of Raw Material in Store? If so, this opportunity could be for you! Join us in Bhiwadi at Ahlcon Parenterals, a pioneer in medical devices, where your skills and experience will be recognized and celebrated. Take the next step in your career with us and help shape the future of healthcare! As a Store Officer at B. Braun Group you will play a vital role in efficient dispensing, physical verification, RM Store temperature monitoring as per SOP. Your key responsibilities: Dispensing of Raw Material as per BMR. Physical verification of Raw materials. Maintain clean record, temperature monitoring of RM Store and Dispensing area. Issuance of material as per FEFO and calculation of material. Maintaing dispensing and raw material store clean and presentable for audit. What you will bring to the team: Strong knowledge of receipt and dispensing of raw material in Store. Experience in inventory management, documentation, and Audit related to store activities. A Bachelor's degree in Pharmacy or a Bachelor of Science or a Master of Science in a relevant scientific discipline (e.g., Chemistry, Biology, Microbiology, Pharmacology) provides a strong foundation for the role. With 2-5 years of experience, you bring valuable hands-on knowledge of industry processes and best practices. What sets B. Braun apart? Ahlcon Parenterals (India) Limited is a B. Braun group company, located at Bhiwadi, Rajasthan. We are a major pharmaceutical formulation manufacturer of both Large and Small Volume Parenterals (LVP and SVP) for domestic and export markets. Our core values of Innovation, Efficiency, Sustainability, Trust, Accountability, and Diversity foster a performance-driven culture where we challenge each other constructively to grow personally and professionally. Recognized through awards such as 'Dream Companies to Work For' and 'Great Place to Work,' we invite you to join our team driven by a shared vision - to protect and improve the health of people around the world. What can we offer you? Convenient transport and subsidized canteen services. Mediclaim and Life Insurance. Learning programs and workshops to drive your development. Mental Wellness Support with counselling and mindfulness sessions. Paternity & Birthday Leave for life’s special moments. Fun activities and team building events. What’s next? Upon receiving your application, our dedicated Talent Acquisition team will review your application. If you stand out, you’ll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead you into our seamless onboarding experience. Join us and be part of something extraordinary! We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are. To find out more about our commitment to diversity click here Check us out on social media! B. Braun Group LinkedIn B. Braun India Facebook B. Braun Group YouTube

Main responsibilities: Provide scientific expertise and build knowledge-based relationships with Key Opinion Leaders (KOLs) to advance medical practice and research for societal benefit, enhancing Pfizer’s image in the scientific community. Act as an interface with identified scientific leaders, building regional relationships to contribute to understanding diseases, research trends, clinical practice guidelines, and treatment patterns. Educate healthcare professionals about specific drugs or medical devices, answering their scientific questions and ensuring products are used effectively. Collect insights from KOLs regarding product usage, unmet needs, and potential areas for research, feeding this information back to internal teams (marketing, sales, clinical development). Stay informed of the latest scientific research and clinical developments in their therapeutic area. Collaborate with internal teams, including marketing, sales, clinical research, and medical information, to ensure consistent and accurate messaging. Implement the medical activities relevant to brand plan strategies for specific products and therapy areas. Participate in and provide medical inputs for KOL meetings, advisory boards, customer pre-launch and launch meetings (CLMs). Conduct/facilitate round table meetings/group discussions and CMEs as a speaker/moderator for assigned therapy areas/products. Support sales force training by providing medical expertise Skill set: Basic knowledge of the pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines Knowledge of “pharmaceutical medicine” including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics, and relevant therapeutic areas/products Communication skills, both written and verbal (including medical writing and presentation skills) Analytical skills and reasoning, and sound medical judgment/decision making Interpersonal skills, internal & external networking, and the ability to impact and influence & present complex information clearly and concisely to diverse audiences Experience in neurology and gastrology therapy area are preferred. Managerial: N/A Certifications: N/A Education: Graduate/Post Graduate in Medicine or other medical sciences (e.g., MBBS, MD in Pharmacology or Community Medicine, PhD in allied sciences, MPH etc.) Work Location Assignment: Remote - Field Based Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Medical Show more Show less

Main responsibilities: Provide scientific expertise and build knowledge-based relationships with Key Opinion Leaders (KOLs) to advance medical practice and research for societal benefit, enhancing Pfizer’s image in the scientific community. Act as an interface with identified scientific leaders, building regional relationships to contribute to understanding diseases, research trends, clinical practice guidelines, and treatment patterns. Educate healthcare professionals about specific drugs or medical devices, answering their scientific questions and ensuring products are used effectively. Collect insights from KOLs regarding product usage, unmet needs, and potential areas for research, feeding this information back to internal teams (marketing, sales, clinical development). Stay informed of the latest scientific research and clinical developments in their therapeutic area. Collaborate with internal teams, including marketing, sales, clinical research, and medical information, to ensure consistent and accurate messaging. Implement the medical activities relevant to brand plan strategies for specific products and therapy areas. Participate in and provide medical inputs for KOL meetings, advisory boards, customer pre-launch and launch meetings (CLMs). Conduct/facilitate round table meetings/group discussions and CMEs as a speaker/moderator for assigned therapy areas/products. Support sales force training by providing medical expertise Skill set: Basic knowledge of the pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines Knowledge of “pharmaceutical medicine” including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics, and relevant therapeutic areas/products Communication skills, both written and verbal (including medical writing and presentation skills) Analytical skills and reasoning, and sound medical judgment/decision making Interpersonal skills, internal & external networking, and the ability to impact and influence & present complex information clearly and concisely to diverse audiences Experience in neurology and gastrology therapy area are preferred. Managerial: N/A Certifications: N/A Education: Graduate/Post Graduate in Medicine or other medical sciences (e.g., MBBS, MD in Pharmacology or Community Medicine, PhD in allied sciences, MPH etc.) Work Location Assignment: Remote - Field Based Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Medical Show more Show less

As a B.Pharm 3rd-year student, I assist in basic pharmaceutical tasks such as drug dispensing, inventory management, and research support. I have foundational knowledge in pharmacology and formulation, with a strong interest in healthcare, patient care, and medical research. Eager to apply my skills in a clinical or research setting to gain hands-on experience and contribute to the healthcare field. Show more Show less

Jubilant Biosys is hiring for Senior Research Associate - In Vivo Biology Experience : 5-8 Years Qualification : M. Pharmacy (Pharmacology) Responsibilties : Drug discovery in pre-clinical pharmacology, In-vivo pharmacology, Animal model development and Efficacy study and Pharmacological screening of Pharmaceutical drug molecules in the respective therapeutic areas such as CNS/ Metabolic disorder/ Autoimmune/Inflammatory diseases/ Pain/Oncology in Drug Discovery field. Evaluation of NCEs in target engagement and efficacy models. Responsible for writing of Protocols, uploading of the data, Lab note book record keeping. SOP writing Exploring scientific journals in order to find new ways/techniques to develop the animal models in a robust and reproducible manner. Follow the guidelines followed in the lab towards different safety aspects and help the lab head in designing the new guidelines. Follow ethical guidelines towards assay validation, data analysis and maintenance.

We are a start-up company offering B2B online marketplace platform connecting medical consumables & devices distributors and manufacturers with healthcare providers such as hospitals, clinics etc. Kogland is a subsidiary of Fingent Corporation and located inside Carnival Info park, Kochi. Skill Set Requirement: Should hold a B. Pharm / D Pharm degree. Should have experience in dispensing drugs for at least 5 years in an offline store. Thorough understanding of dosage administration and measurement, Integrity and compassion. Should have permanent address in Tamil Nadu(Chennai Preferred) as per address proof and currently based out of Kerala( or ready to move to Cochin), Roles and Responsibilities: Review and execute physician s prescriptions checking their appropriateness and legality Listen carefully to customers to interpret their needs and issues and offer information and advice Keep records of patient history and of all activities regarding heavy medication Support Drug Inspector with required documents and sample during inspection Comply with all applicable legal rules, regulations and procedures