Pharmacy Jobs

Role & Responsibilities • Develop and adapt health economic models (cost-effectiveness, cost-utility, cost-minimisation, and budget impact) • Conduct systematic, targeted, or structured literature reviews to gather inputs for economic models • Assist with submissions to Health Technology Assessment (HTA) agencies • Write detailed technical reports for health economic models • Perform quality checks on models developed by other health economists • Identify, extract, analyze, and summarize data from various sources • Summarize model methodology and findings in reports and slide-decks • Communicate effectively with clients and internal teams to ensure timely and smooth project execution • Provide writing support for publications based on HEOR studiesExperience: 2+ years in Health Economics and Outcomes Research (HEOR) Skills • Strong expertise in health economic modeling (cost-effectiveness, cost-utility, cost-minimisation) • Experience with systematic literature reviews and data analysis • Proficiency in health economics tools and software • Strong communication and collaboration skills • Ability to write clear, concise, and detailed reports About The Company • Skyward Analytics is a leading company in health economics and outcomes research, providing solutions to healthcare challenges through advanced analytics.The company offers a flexible work environment, allowing for both full-time and part-time roles, with opportunities for hybrid and remote work. Skyward Analytics emphasizes innovation and collaboration to drive impactful health solutions.

Role & Responsibilities • Conduct comprehensive health data analysis across patient charts, claims databases, and electronic hospital records to support real-world evidence (RWE) initiatives • Develop and apply advanced statistical and machine learning techniques to generate actionable insights • Contribute to retrospective database analyses to support medical affairs, market access, and clinical development • Draft and review technical reports, abstracts, manuscripts, protocols, SAP, and presentations based on RWE findings • Collaborate cross-functionally to define research questions, study designs, and analytical approaches • Present complex analytical findings to internal and external stakeholders in a clear and impactful manner • Contribute to thought leadership through publications, conference presentations, and internal knowledge sharing • Ensure rigorous project management across timelines, budgets, and quality standards • Deliver on projects involving new technologies like Causal Inference, Digital Twins, and Generative AI Skills • Proficiency in inferential statistics, predictive modeling, and machine learning techniques (preferred) • Expertise in SQL, Python, R, and data visualization tools; familiarity with Excel, PowerPoint, and Word • Strong problem-solving skills with the ability to adapt analytical strategies to evolving business needs • Excellent written and verbal communication skills • Ability to lead projects independently and engage key stakeholders effectively • Strong understanding of therapeutic areas and disease treatment pathways Qualifications • 3-8 years of global experience in RWE analytics, healthcare data science, or related fields within life sciences or consulting About The Company • Axtria is a global leader in life sciences analytics, leveraging advanced technologies like AI/ML to address healthcare challenges. Axtria offers a collaborative work environment, fostering innovation and knowledge sharing without hierarchical boundaries.

Role & Responsibilities • Refine literature review questions in alignment with the team lead and prepare research protocols • Design literature searches for electronic databases (e.g., PubMed, EMBASE, Cochrane Library) and grey literature (e.g., conference proceedings, regulatory sites) • Screen abstracts and full-texts to determine relevance based on PICO criteria • Create and review PRISMA diagrams to document full-text study selection • Extract data from included articles into predefined data extraction templates • Draft evidence tables, figures, final reports, and presentation decks, interpreting patterns and trends • Ensure the quality of assigned work • Support and maintain effective relationships with key stakeholders • Work effectively with global HEOR teams across various time zones Skills & Competencies • Excellent written and oral communication skills in English, with the ability to tailor content to different stakeholders • Experience in medical writing is a plus • Skilled in EndNote or other reference management tools (preferred) • Proficiency with Microsoft Office (Word, PowerPoint, Excel) • Strong attention to detail and strong editing/fact-checking abilities • Experience in systematic review tools and citation databases (e.g., PubMed, EMBASE) • Ability to manage multiple projects efficiently and prioritize tasks across different stages of the process • Experience with innovative use of artificial intelligence to boost efficiency in systematic reviews • Collaborative and team-oriented, with the ability to work across global teams and time zones Qualifications • Bachelor’s or Master’s degree in pharmacy, health economics, public health, medicine, epidemiology, or a related health sciences field Experience • 3+ years of experience in systematic literature review methods for Master's degree holders • 5+ years of experience in systematic literature review methods for Bachelor's degree holders • Experience in conducting various types of literature reviews (clinical, economic, QoL, burden of illness, etc.) • Proficiency in biomedical databases (e.g., MEDLINE, Embase) • Strong understanding of research principles and implementation About The Company • Amgen is a global biotechnology company committed to unlocking the potential of biology for patients suffering from serious illnesses.

Role & Responsibilities • Collaborate with HEOR core team leaders to ensure alignment of HEOR deliverables with the Health Outcomes Research Plan (HORP) and broader company strategies • Facilitate change management processes for HEOR projects, ensuring scope alignment and budget compliance • Provide strategic and tactical updates to HEOR Operations Steering Team • Partner with scientists, leadership, and business partners to ensure timely, on-budget execution of HEOR projects • Track project progress and ensure quality and compliance deliverables are met • Deliver cross-functional results through project management, influence, and communication skills • Facilitate project reviews, identify bottlenecks, and resolve issues to ensure smooth execution • Lead retrospective project/process review meetings to identify strengths and areas for improvement • Contribute to process improvements and share best practices across teams Skills • Applied knowledge of project management tools and processes • Strong proficiency in Microsoft Office (Word, Excel, PowerPoint), Microsoft Project • Ability to translate complex scientific information into clear and concise communication • Strong problem-solving skills and ability to resolve cross-functional issues • Excellent organizational and self-management skills • Ability to influence and collaborate across teams • Experience in managing cross-functional projects Qualifications • Bachelor’s or Master’s degree in Pharma, Science, or MBA • 7-10 years of experience in Project Management, preferably in HEOR or related fields • Knowledge of drug development processes and therapeutic areas • Previous experience with project management tools (Planisware, SAP, Salesforce) is preferred • PMP certification or higher degree in project management is a plus • Experience with Six Sigma (Green Belt/Black Belt) and critical chain project management principles is preferred About The Company • Eli Lilly and Company is a global healthcare leader headquartered in Indianapolis, Indiana. The company is dedicated to discovering and delivering life-changing medicines and improving the understanding and management of diseases worldwide.

Role & Responsibilities • Lead regulatory submissions and ensure compliance with local and international regulations • Prepare and review regulatory dossiers and submissions for product approvals • Communicate with regulatory agencies to resolve issues related to product submissions • Support the regulatory strategy for new product development • Monitor changes in regulations and provide guidance to internal teams Qualification: Degree in Life Sciences / PharmacyExperience: 2-3 years Skills • Strong knowledge of regulatory affairs and submission processes • Experience in product registrations and renewals • Proficient in using regulatory tools and software • Strong communication skills in English & Hindi • Ability to manage multiple projects and priorities About The Company • The company is expanding its regulatory affairs team to support business growth. The company provides a collaborative environment and opportunities for career advancement. With a focus on compliance and business development, the company serves clients across various sectors.

Role & Responsibilities • Assist in the preparation and submission of regulatory documents • Monitor and ensure compliance with regulatory requirements • Support the regulatory team in product registrations and renewals • Maintain communication with regulatory agencies and stakeholders • Assist in compiling and reviewing technical documentation Qualification: Relevant degree in Life Sciences / PharmacyExperience: Freshers Skills • Basic computer skills • Strong communication skills in English & Hindi • Attention to detail and organizational skills • Willingness to learn and adapt to regulatory practices About The Company • A growing team dedicated to regulatory affairs and business development. A dynamic environment focused on delivering quality services and ensuring compliance. The company values innovation, collaboration, and growth within the life sciences industry.

Role & Responsibilities • End-to-end ICSR processing • Safety case follow-up and submissions • Adhere to client and global regulatory guidelines • Conduct internal quality checks and documentation Qualification: B.Pharm / Life SciencesExperience: 1-3 years Skills • Knowledge of ICSR processing and safety case management • Familiarity with regulatory guidelines in Pharmacovigilance • Attention to detail and strong organizational skills • Ability to work in a compliance-driven, fast-paced environment About The Company • Accenture is a global leader in life sciences operations, focusing on regulatory services and pharmacovigilance. The company offers structured growth opportunities in the life sciences sector. Accenture fosters a diverse and inclusive work environment while collaborating with leading biopharma clients.

Role & Responsibilities • Translate Japanese safety cases to English • Prepare Japan HA E2B reports • Conduct case quality review, follow-ups, and submissions • Ensure SLA and quality compliance for Japan foreign cases Qualification: Life Sciences / Pharmacy / Any Graduate Language Requirement: Japanese (JLPT N5 or above)Experience: 1-3 years Skills • Japanese language proficiency (JLPT N5 or above) • Knowledge of Pharmacovigilance operations • Experience in case quality review and regulatory submissions • Attention to detail and compliance mindset About The Company • Accenture provides global exposure in pharmacovigilance, working with leading biopharma clients. The company fosters a collaborative and inclusive workplace. Accenture offers structured career growth opportunities and a focus on compliance-driven roles.

Role & Responsibilities • ICSR case intake and data entry • MedDRA coding and safety database management • Case processing and regulatory submissions • Compliance with global PV regulations (ICH, GVP)Qualification: B.Pharm / Life SciencesExperience: 0-1 year (Freshers eligible) Skills • Knowledge of Pharmacovigilance operations • Familiarity with MedDRA coding and safety databases • Attention to detail and compliance-driven mindset • Ability to work in rotational shifts About The Company • Accenture offers structured learning and growth opportunities in pharmacovigilance. • The company specializes in life sciences regulatory services and has a strong global presence. • Accenture works with leading biopharma clients and promotes an inclusive work culture.

Role & Responsibilities • Prepare and manage global regulatory submissions (eCTD) • Handle lifecycle management submissions (CMC, SPL, amendments) • Coordinate documentation for global health authority filings • Ensure regulatory compliance and audit readinessQualification: B.Pharm / M.PharmExperience: 1-3 years Skills • Knowledge of regulatory processes and global submissions • Proficiency in eCTD publishing, Veeva Vault, DocuBridge • Strong attention to detail and compliance mindset • Excellent communication and coordination skills About The Company • Accenture is a global leader in professional services and life sciences operations. • The company offers structured growth, global exposure, and compliance-driven roles aligned with international regulatory standards. • Accenture provides an inclusive and equal-opportunity workplace, working with leading biopharma clients.

Roles & Responsibilities:• Convert medical records into numeric or alphanumeric codes using ICD-10-CM, CPT, and HCPCS• Accurately review and analyze patient medical records for coding compliance• Ensure proper documentation and coding accuracy as per healthcare standards• Work closely with quality and audit teams to maintain coding accuracy• Follow HIPAA guidelines and maintain patient data confidentiality• Participate in training programs and continuous learning sessions• Meet productivity and quality benchmarks defined by the organizationQualification:• UG / PG in Life Sciences, Paramedical, or Allied Healthcare fieldsEligible Backgrounds:• Nursing Freshers (GNM / DGNM / Staff Nurse)• Pharmacy Freshers (B.Pharm / D.Pharm / M.Pharm)• Physiotherapy (BPT)• Dentistry• Life Sciences• Biotechnology• Microbiology• Biomedical / Biomedical Engineering• Biochemistry• Bioinformatics• Botany / Zoology• Optometry• Radiology / Anesthesia (Allied Health)Experience:• Freshers or candidates with up to 2 years of experienceSkills:• Basic knowledge of medical terminology• Interest in medical coding and healthcare documentation• Willingness to learn ICD-10-CM, CPT, and HCPCS coding standards• Good analytical and attention-to-detail skills• Ability to work in a structured, process-driven environmentPerks & Benefits:• Incentives up to ₹5,000• Insurance coverage• Provident Fund (PF)• Career growth opportunities in Medical CodingAbout the Company:OMS Healthcare is an ISO 9001:2015 certified organization delivering high-quality medical coding services to the healthcare industry. The company specializes in Risk Adjustment Coding and is driven by a team of skilled professionals focused on accuracy, compliance, and continuous improvement. OMS Healthcare offers excellent training, career development, and long-term growth opportunities for freshers entering the medical coding domain.

Role & Responsibilities • Engage with Medical Experts (MEs) to educate them on medical/scientific information • Identify and map MEs/Key Accounts, pinpointing opportunities to involve MEs when a specific medical need arises • Develop and execute ME engagement plans aligned with the country strategy • Respond to unsolicited requests for information from MEs • Support Novartis clinical research programs and optimize trial execution • Provide scientific educational support to potential and actual study sites in collaboration with clinical operations • Serve as a medical resource to field matrix colleagues • Report technical complaints, adverse events, or special case scenarios related to Novartis products within 24 hours of receipt • Be flexible to be on the field (80%) across key areas within Egypt Qualifications • Medical Degree (MD), Ph.D. in Pharmacy, or PharmD is required Experience • 0-3 years of experience in a medical role is preferred Skills • Strong scientific knowledge and ability to educate Medical Experts on medical/scientific information • Ability to collaborate with clinical research teams and study sites • Excellent communication and interpersonal skills • Flexibility to engage in fieldwork (80% travel across Egypt) • Ability to handle adverse event reporting and technical complaints in compliance with company protocols About The Company • Novartis is a global healthcare company focused on reimagining medicine to improve and extend lives. The company is committed to providing high-quality medicines and is recognized for its strong research and development capabilities.

Role & Responsibilities • Conduct hands-on analyses using large-scale secondary data sources such as claims, EHR, and registries • Develop study protocols and statistical analysis plans (SAPs) for Real-World Data (RWD) studies • Perform data cleaning, transformation, and statistical modeling using tools like SAS, R, and Python • Interpret and report results in a scientifically sound and business-relevant manner • Adhere to timelines, manage data deliverables, and communicate effectively with internal and external partners • Stay updated on the latest data and methodological standards, contributing insights to HEOR data strategies Qualifications • Master's degree or higher in Epidemiology, Biostatistics, Health Economics, Public Health, or a related field Experience • 5+ years of hands-on experience in RWD analysis using claims, EHR, or registry data • Strong experience in writing protocols, SAPs, and scientific reports Skills • Proficiency in statistical software (e.g., SAS, R, Python) and data visualization tools • Excellent communication and interpersonal skills • Ability to manage multiple priorities and work collaboratively across teams • Familiarity with budget impact modeling and basic health economic calculations is a plus About The Company • Alcon is a leading innovator in the eye care industry, dedicated to providing products and solutions that improve sight and lives. The company offers a collaborative and intellectually stimulating environment focused on advancing HEOR strategies globally.

Role & Responsibilities • Plan and manage material requirements planning (MRP) for production • Ensure timely availability of materials for production, maintaining optimal inventory levels • Coordinate with cross-functional teams to ensure smooth production processes • Monitor inventory levels, ensuring material availability and minimal excess stock • Collaborate with production and procurement teams to address material shortages or excesses • Drive process improvements to enhance production efficiency • Report and analyze inventory data to ensure operational excellence Qualifications • Bachelor's degree in Supply Chain Management, Logistics, or related field • Proven experience in MRP, material planning, production planning, and inventory control • Exposure to US market regulatory and operational requirements Experience • Minimum 3-5 years of experience in a formulation manufacturing environment • Strong proficiency in SAP for planning, procurement, and inventory transactions • Experience managing cross-functional collaboration and handling multiple priorities Skills • Strong communication and coordination skills • Analytical mindset with the ability to interpret data and anticipate material risks • Detail-oriented with a focus on operational excellence • Ability to manage fast-paced manufacturing operations About The Company • Alembic Pharmaceuticals is a leading global player in the pharmaceutical industry, specializing in the manufacturing of high-quality formulations.

Role & Responsibilities Identify, develop, and maintain collaborative relationships with KOLs, scientific experts, and other medical stakeholders. Deliver high-quality medical and scientific communications in line with defined communication plans. Create and execute stakeholder engagement plans, adhering to Sobi’s high standards. Support the country Hemophilia team in developing local medical tactics and provide input to HQ/regional plans if relevant. Organize and set up scientific advisory boards with key stakeholders, in collaboration with HQ. Work with the local patient access team to support local access. Contribute and support medical scientific aspects in various activities locally and regionally. Provide local and regional feedback to Regional office when performing Business Development Due Diligence. Coordinate ISSs and NPU as appropriate. Handle medical information enquiries in collaboration with HQ in Stockholm. Attend relevant local, regional, and global congresses and symposiums to represent Sobi and interact with stakeholders. Represent the scientific interests in internal and external forums and interact with KOLs at hospitals, patient associations, and other NGOs within the therapeutic area. Maintain and develop strong relationships with scientific societies and central decision-makers at local health authorities. Provide advice to the organization and management on medical matters and their legal implications. Ensure that medical and scientific knowledge for the therapeutic area remains at the forefront of contemporary thinking. Report to management in accordance with Sobi requirements and standards. Lead a team of Medical Science Liaisons (MSLs) and provide medical leadership with partners. Qualification Bachelor's degree in a medical field (Pharmacy, Medicine); postgraduate degree preferred. Experience 8+ years of experience in the medical function within the Pharmaceutical Industry. Experience in Haematology & Rare diseases field; GCC markets experience is a plus. Demonstrated ability to manage a diversified portfolio and meet medical KPIs. Skills Fluency in written and spoken English & Arabic. Proficiency in Microsoft Office suite. Strong operational discipline and execution skills. Alignment with Sobi core values: Care, Ownership, Urgency, Partnership, Ambition. About The Company Sobi - Swedish Orphan Biovitrum AB (publ) is a global biopharmaceutical company focused on providing innovative therapies for rare diseases. Sobi’s commitment to science and collaboration enables them to deliver life-changing treatments to patients worldwide. Their culture is driven by a desire to make a positive impact on the world’s most challenging health conditions, with a focus on rare diseases.

Role & Responsibilities • Review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. • Review includes coding, assessment of seriousness, expectedness, and causality. • Write Company comments, follow-up questions, and analyze similar events. • Complete all required supporting documentation, such as trackers. • Support the Qualified Person for Pharmacovigilance (if not medically qualified) in the medical understanding and evaluation of any safety issues. • Review and provide input in periodic reports. • Review literature screening search strategies and review articles to determine if they contain ICSRs/SAEs related to the relevant Medicinal Product or other safety-related findings. Qualification • MD qualification is required. Experience • Proven ability to plan, organize, prioritize, and execute multiple tasks efficiently. Skills • Ability to work cross-culturally and cross-functionally, valuing teamwork. • Strong communication and presentation skills. • Advanced English skills, both verbal and written (at least B2 level). • Advanced knowledge of MS Office. About The Company • PrimeVigilance offers an opportunity for Medical Doctors to develop a career in Drug Safety.The company’s Pharmacovigilance Physician team operates across North America, Europe, and Asia, providing global pharmacovigilance services. PrimeVigilance is focused on creating a collaborative, high-quality environment for physicians interested in pharmacovigilance.

Role & Responsibilities • Author medical writing tasks, including aggregate reports, Risk Management Plans (RMPs), and other documents throughout the product’s life cycle. • Responsible for the quality and content of documents, as well as quality control review of documents prepared by medical writing peers. • Engage in continuous self-education regarding all aspects of medical writing activities. • Actively participate in training sessions, maintenance, and development of quality system documents. • Support pharmacovigilance operations associated with medical writing. Qualification • PhD or MSc in Life Sciences or Healthcare (e.g., pharmacy, biology, chemistry, veterinary medicine). Experience • Previous experience in drug safety medical writing, including PBRERs, DSURs, and RMPs. Skills • Strong time management, organization, and multitasking skills with excellent attention to detail. • Strong communication and presentation skills. • Advanced knowledge of MS Office. • Fluency in English (both verbal and written). About The Company • PrimeVigilance offers an opportunity for medical writers to further develop their careers in pharmacovigilance medical writing.

Role & Responsibilities • Review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports for medical and causality assessments. • Assess the seriousness, expectedness, and causality of reports. • Write company comments, follow-up questions, and perform analysis of similar events. • Complete required supporting documentation such as trackers. • Support the Qualified Person for Pharmacovigilance (QPPV) in evaluating safety issues (if not medically qualified). • Provide input for periodic reports. • Review literature screening search strategies and articles to determine safety findings or ICSRs/SAEs related to the relevant medicinal products. Qualification • MD (Medical Doctor) Experience • Experience in Pharmacovigilance, preferably with exposure to ICSR handling and safety reporting • Strong understanding of drug safety regulations and practices Skills • Ability to plan, organize, prioritize, and execute multiple tasks • Strong communication and presentation skills • Ability to work cross-culturally and functionally as part of a global team • Advanced English skills (both verbal and written), at least B2 level • Advanced knowledge of MS Office About The Company • PrimeVigilance is a global pharmacovigilance and drug safety service provider. The company offers an opportunity for medical doctors to build and develop their careers in drug safety.

Roles & Responsibilities: • Manage end-to-end TMF and document management operations in compliance with ICON SOPs, client requirements, and regulatory guidelines • Lead and mentor 20–30 TMF professionals, ensuring high performance and quality delivery • Coordinate TMF activities across multiple studies and clients • Generate and present TMF status reports for internal stakeholders and clients • Drive process improvement initiatives to enhance efficiency and quality • Ensure TMF inspection readiness and participate in internal and external audits • Oversee TMF archiving activities and study close-out documentation • Liaise with clinical study teams, training departments, and clients • Manage quality control, tracking, and compliance metrics • Support departmental and cross-functional projects as assigned Qualification: • Bachelor’s degree in Science, Medicine, Pharmacy, Life Sciences, or equivalent • Strong understanding of clinical study start-up, maintenance, and close-out activities Experience: • 12+ years of experience in TMF Operations within clinical research or CRO environments • 3+ years of people management experience managing large teams (20–30 members) Skills: • Excellent organizational, communication, and stakeholder management skills • Proven ability to manage multiple projects and global clients • Strong analytical, problem-solving, and conflict management skills • Willingness to travel up to 25% (domestic/international) About the Organisation: ICON plc is a global leader in healthcare intelligence and clinical research, known for its strong culture of Accountability, Collaboration, Partnership, and Integrity. ICON provides professionals the opportunity to work on global clinical trials, shaping the future of drug development while delivering high-quality solutions to clients worldwide.