Pharmacy Jobs

Role & Responsibilities • Coordinate day-to-day clinical trial activities at the site • Assist investigators during study initiation, conduct, and close-out • Maintain essential trial documents including ISF, CRFs, and logs • Ensure compliance with ICH-GCP, SOPs, and study protocols • Support subject recruitment, informed consent, and follow-ups • Coordinate with monitors, sponsors, and ethics committees • Handle data entry, query resolution, and audit readiness Qualifications & Experience • Degree in Life Sciences, Pharmacy, Nursing, or related field • 6 months – 1 year of experience in clinical research or CRC role • Practical knowledge of clinical trials, GCP, and regulatory guidelines Skills • Strong documentation and organizational skills • Good patient coordination and communication abilities • Ability to work in compliance-driven clinical environments About the Company • JSS Research is a reputed clinical research organization supporting regulated clinical trials in metro cities across India

Role & Responsibilities • Oversee, manage, and coordinate clinical trials as per approved protocols and regulatory requirements • Obtain informed consent and ensure adherence to ethical clinical research practices • Manage study protocols and maintain strict documentation standards • Ensure regulatory compliance throughout the study lifecycle • Maintain accurate and up-to-date study records and research documentation • Coordinate with investigators, medical staff, and multidisciplinary research teams • Support smooth execution and timely completion of clinical research activities Qualifications & Experience • B.Pharm, M.Pharm, PharmD, B.Sc / M.Sc Life Sciences or related field • Demonstrated clinical research or clinical trial experience • Strong knowledge of ICH-GCP and regulatory requirements Skills • Excellent documentation and record-keeping abilities • Strong organizational, time management, and problem-solving skills • Effective communication and stakeholder coordination skills • Ability to work collaboratively within multidisciplinary teams Preferred • Advanced degree or certification in clinical research About the Company • Research-focused clinical organization based in Prayagraj conducting regulated clinical trials

Role & Responsibilities • Conduct off-site monitoring visits during study phases • Perform Site Initiation Visits (SIVs) and ensure study readiness • Review protocol prerequisites and site compliance • Execute routine monitoring as per study monitoring plans • Coordinate with sites for feasibility assessments • Prepare and submit study-related reports (SIV, monitoring, close-out, etc.) • Collect and manage essential trial documents • Review trial documents for SOP, protocol, and regulatory compliance • Train and mentor teams on ICH-GCP and regulatory updates • Support internal and external audits and inspections Qualifications & Experience • Degree in Life Sciences, Pharmacy, or Clinical Research • 1-3 years of experience as a Clinical Research Associate or equivalent • Strong knowledge of ICH-GCP guidelines • Experience in clinical trial monitoring and CRO operations • Excellent documentation, communication, and coordination skillsSkills • Proficient in ICH-GCP and regulatory compliance • Strong organizational and time-management skills • Ability to analyze clinical trial data and resolve issues • Good problem-solving and decision-making skills • Excellent communication skills (verbal and written) • Detail-oriented with strong documentation skills About the Company • Veeda Clinical Research is a well-established CRO in India, supporting global and domestic clinical trials across multiple therapeutic areas, offering strong career-building opportunities for aspiring CRAs.

Role & Responsibilities • Ensure smooth day-to-day operations of clinical trials at the site • Collect, review, and update clinical trial data daily • Share weekly updates on data collection and trial progress • Manage query response and ensure timely resolution • Coordinate patient follow-ups and visit schedules • Maintain compliance with ICH-GCP, SOPs, and regulatory requirements • Support investigators and sponsors during trial execution Qualifications & Experience • B.Pharm (Bachelor of Pharmacy) / M.Pharm (Master of Pharmacy) • 0-3 years of experience in clinical research or clinical trials • Sound knowledge of ICH-GCP guidelines • Good documentation and data management skills • Strong communication and coordination abilities About the Company • Micro Data Labs is a leading Clinical Research Organization (CRO), providing clinical trial management and operations in compliance with ICH-GCP guidelines.

Role & Responsibilities • Recruit and enroll eligible study participants • Coordinate patient visits, procedures, and follow-ups as per study protocol • Enter and maintain clinical research data in electronic data capture (EDC) systems • Address protocol-related queries from study participants • Ensure compliance with ICH-GCP, ethical guidelines, and regulatory requirements • Prepare, maintain, and update essential study documentation • Archive Case Report Forms (CRFs) and trial-related documents properly • Coordinate with sponsors, ethics committees, investigators, and study sites • Support Principal Investigators (PI) for smooth study conduct Qualifications & Experience • Bachelor’s or Master’s degree in Biotechnology, Biochemistry, Microbiology, Biology, Life   Sciences, Nursing, or Pharmacy • Diploma in Clinical Research (optional) • 1–5 years of experience in clinical research coordination • Strong understanding of clinical trial processes and documentation • Proficiency in MS Word and MS Excel • Good communication and interpersonal skills About the Company • Indira IVF Hospital is one of India’s leading fertility and reproductive healthcare organizations,    known for its hospital-based clinical research and patient-centric trials.

Key ResponsibilitiesReview and evaluate AEs and SAEs; perform first-line clinical assessmentPrepare SAE narratives and collect follow-up safety informationMonitor and report safety data from trials, RWE, spontaneous reports, and literatureSupport DSMB / Safety Review Committee activitiesEnsure timely regulatory safety submissions (FDA, EMA, etc.)Maintain and reconcile safety databasesPerform MedDRA and WHO Drug codingContribute to SaMPs, protocols, SOPs, and CRFsEnsure compliance with GCP, GVP, and global regulationsParticipate in audits and quality improvement initiativesQualificationsBachelor’s degree in Pharmacology, Nursing, Life Sciences, or related field1–2 years experience in Pharmacovigilance / Clinical Safety preferredFreshers considered with relevant internships, projects, or PV certificationsRequired SkillsStrong knowledge of GCP, GVP, and GxP principlesGood clinical judgment and scientific writing skillsHigh attention to detail and strong organizational skillsEffective communication and teamwork in global settingsWhy Emmes GroupGlobal CRO with strong scientific reputationExposure to international trials and regulatory workLearning-focused culture and career growth opportunities

Role & Responsibilities • Review and verify medication orders for safety and effectiveness • Interpret medication orders for clarity, accuracy, and patient suitability • Prepare, compound, and dispense medications, including pediatric, IV admixtures, TPN, and chemotherapy therapies • Conduct final checks on medications and maintain accurate records • Provide patient counseling on proper medication use • Ensure secure storage and handling of narcotics and controlled drugs • Collaborate with healthcare professionals to promote cost-effective medication use • Respond to medication-related queries, incidents, and adverse drug reactions • Ensure compliance with regulatory requirements and maintain hygiene and equipment functionality Qualifications & Experience • Bachelor of Pharmacy (BPharm) from an accredited institution • Current National License • 1-4 years of experience in a pharmacy setting About the Company • Sheikh Shakhbout Medical City is a premier healthcare provider in Abu Dhabi, committed to delivering high-quality medical and pharmacy services.

Role & Responsibilities • Accurately interpret and dispense prescriptions • Provide expert advice on medication usage and side effects • Ensure medications are dispensed in compliance with UAE laws and clinic policies • Counsel patients on correct medication usage, storage, and precautions • Address patient inquiries about medications and treatment options Qualifications & Experience • Bachelor’s degree in Pharmacy (BPharm or equivalent) • Valid UAE pharmacy license • Minimum of 2 years of experience as a licensed pharmacist • Strong knowledge of pharmaceuticals, medical terminology, and safety regulations • Excellent communication and customer service skills About the Company • Yas Clinic Group is a leading healthcare provider in the UAE, committed to delivering high-quality medical and pharmacy services to the community.

Role & Responsibilities • Receive, review, and accurately dispense prescriptions and medication orders • Verify prescriptions for appropriateness, dosage, and potential interactions • Counsel patients on medication usage, side effects, storage, and precautions • Provide guidance to healthcare professionals on drug therapies • Monitor and assess patient medication therapy to optimize outcomes • Detect and prevent adverse drug interactions and medication errors • Manage inventory, ensure proper storage of medications, and restock as needed • Maintain accurate patient medication records and ensure compliance with laws and regulations • Participate in quality assurance, audits, and continuous improvement initiatives Qualifications & Experience • Bachelor of Pharmacy (BPharm) • 1-7 years of experience in a pharmacy setting • Strong communication skills and patient counseling abilities About the Company • Tawteen provides healthcare services in Muscat, Oman, committed to ensuring safe and effective medication management for patients.

Role & Responsibilities • Accurately interpret and dispense prescriptions • Provide expert advice on medication usage and potential side effects • Ensure proper storage, labeling, and dispensing of medications • Maintain accurate records of all prescriptions and transactions • Offer excellent customer service and ensure patient satisfaction • Collaborate with the healthcare team to ensure optimal patient care Qualifications & Experience • Bachelor's or Master's degree in Pharmacy (BPharm, MPharm) • Valid license or certification to practice as a pharmacist in the UAE • Minimum of 2 years of pharmacy experience, preferably in the UAE • Strong communication and customer service skills • Proficiency in English About the Company • Al Kamal Medical Center is committed to providing high-quality healthcare and pharmacy services to the community.

Role & Responsibilities • Develop clinical manuscripts, abstracts, posters, and presentations • Perform end-to-end scientific and regulatory writing • Manage Veeva Vault / PubConnect / Datavision workflows • Conduct literature searches and plan publications • Coordinate with biostatistics, regulatory, and medical affairs teams • Ensure compliance with journal, congress, and company SOPs • Mentor junior medical writers and perform peer reviews Qualifications & Experience • B.Pharm, M.Pharm, PharmD, MSc Life Sciences, PhD • 4–7 years of experience in medical writing and publication planning • Strong command of ICH guidelines and publication ethics • Familiarity with Veeva Vault MedComms or PromoMats About the Company • Syneos Health is a global biopharmaceutical solutions company, providing an inclusive work culture and opportunities to work on FDA and EMA-approved products, with global exposure across 110+ countries.

Role & Responsibilities • Conduct systematic and ad-hoc literature searches in Embase, PubMed, Medline • Identify Individual Case Safety Reports (ICSRs) from scientific literature • Develop and validate pharmacovigilance search strategies • Perform case triage, data entry, MedDRA/WHODrug coding • Prepare narratives and ensure regulatory compliance (ICH-GCP, GVP) • Generate expedited and periodic safety reports • Support audits, inspections, and TMF/PVSMF documentation • Act as Subject Matter Expert (SME) and mentor team members Qualifications & Experience • B.Pharm, M.Pharm, PharmD, BDS, BMS • Minimum 5 years of experience in pharmacovigilance, including literature case processing • Strong knowledge of global and local pharmacovigilance regulations • Hands-on experience with safety databases • Expertise in literature surveillance and case processing About the Company • Syneos Health is a global leader in biopharmaceutical solutions, working with 94% of FDA-approved novel drugs and offering career growth opportunities for professionals in the field.

Role & Responsibilities • Serve as a liaison to the medical/scientific community, establishing partnerships with Healthcare Providers (HCPs) • Disseminate clinical and scientific information on Novartis compounds in an ethical and stakeholder-focused manner • Implement clinical and educational strategies in collaboration with Novartis colleagues • Address HCP inquiries with the latest emerging data and available resources • Identify and engage Medical Experts and study investigators aligned with the Integrated Product Strategy (IPS) • Educate on Novartis clinical research programs and support trial feasibility and accrual • Facilitate independent research submissions and material transfer agreements • Promote scientific exchange on emerging principles and trends • Report HCP insights to inform medical strategy and IPS planning • Act as a local medical resource and contribute to strategy design and execution • Ensure adherence to compliance processes and foster a diverse, inclusive environment Qualifications & Experience • Degree in PharmD, PhD, or MD (Medical Doctor) • At least 1 year of experience as a Medical Science Liaison (experience in Hematology is a plus) • Fluent in both Arabic and English About the Company • Novartis is a global healthcare company committed to discovering and developing innovative medicines to improve patient outcomes.

Role & Responsibilities • Oversee all pharmacy operations and ensure compliance with regulatory requirements • Develop and implement strategies to optimize medication management processes • Manage inventory and procurement of pharmaceuticals and supplies • Train and supervise pharmacy staff to ensure high-quality service • Stay updated on advancements in pharmacy practice and incorporate best practices • Conduct medication reviews and provide drug information to healthcare providers • Monitor medication safety and implement measures to prevent errors and adverse events • Participate in interdisciplinary committees and contribute to quality improvement initiatives • Evaluate and implement technology solutions to enhance pharmacy operations Qualifications & Experience • Bachelor of Pharmacy (B.Pharm), Master of Pharmacy (M.Pharm) • Active licensure as a pharmacist in the relevant jurisdiction • Board certification in a specialized area of pharmacy practice (preferred) • 10-15 years of experience in pharmacy practice, with at least 5 years in a leadership role Skills • Strong analytical and problem-solving skills • Ability to effectively manage multiple priorities and meet deadlines • Proven leadership abilities and experience in team management • Commitment to continuous professional development and staying current with industry trends • In-depth knowledge of pharmacy regulations, practices, and medication management Preferred • Experience with pharmacy management software and technology solutions • Expertise in medication safety and quality assurance protocols About the Company • Confidential Company in Dubai, UAE is committed to providing high-quality pharmaceutical services with a focus on regulatory compliance, patient safety, and innovation in pharmacy practice.

Role & Responsibilities • Conduct research and analysis in the field of Ayurveda and related subjects • Assist in the preparation of research reports, publications, and scientific papers • Support ongoing research projects and contribute to data collection and analysis • Collaborate with senior researchers and the research team for project execution • Maintain accurate and detailed records of research activities and results • Participate in meetings, discussions, and reviews of research progress Qualifications & Experience • B.Pharm, B.E./B.Tech, M.Pharm from a recognized university • Previous research experience (preferred) Skills • Strong knowledge of research methodologies and scientific principles • Excellent data analysis, report writing, and presentation skills • Ability to work independently as well as in a team-oriented environment • Proficiency in using research tools, databases, and statistical software Preferred • Experience in research in Ayurveda or related fields • Familiarity with laboratory techniques and scientific research protocols How to Apply • Interested candidates should attend the Walk-in Interview at the following venue: Regional Ayurveda Research Institute Nehru Garden, Near Gandhi Bhavan, Kothrud, Pune – 411038, Maharashtra • Ensure that all required documents are brought along for the interview. About the Company • CCRAS (Central Council for Research in Ayurvedic Sciences) is a research organization dedicated to the promotion of Ayurveda through research and development. It focuses on advancing Ayurvedic medicine and healthcare.Official NotificationClick Here

Role & Responsibilities • Manage and oversee engineering projects in Civil, Electrical, and Mechanical domains • Lead project teams, ensuring timely delivery within scope and budget • Develop and maintain project plans, timelines, and budgets • Ensure compliance with all regulations, quality standards, and safety protocols • Coordinate with clients, vendors, and stakeholders for smooth project execution • Track project progress, report issues, and provide solutions to overcome challenges • Manage project documentation, including reports, contracts, and progress updatesName of the PostsVacanciesEducationProject Manager09B.E./B.Tech in Civil, Electrical, and Mechanical Engineering, MBA, B. Pharm, PGDM Skills • Strong knowledge of project management principles and engineering concepts • Excellent leadership, communication, and interpersonal skills • Ability to manage multiple tasks and projects simultaneously • Proficiency in project management software and tools Preferred • Professional certifications in project management (PMP, PRINCE2) are advantageous • Experience with government or large-scale engineering projects About the Company • BPSC (Bihar Public Service Commission) is a government organization responsible for recruiting candidates for various positions across the state of Bihar, ensuring effective governance and service delivery.Starting date08-01-2026Closing date29-01-2026Extended notificationClick HereApplication FormClick Here

Role & Responsibilities • Dispense medications according to prescriptions and ensure proper medication management • Counsel patients on the safe use of medications • Maintain accurate pharmacy records and inventory • Work with healthcare providers to ensure the proper use of drugs Qualifications & Experience • B. Pharm or D. Pharm degree from a recognized university • Previous pharmacy experience (preferred)Vacancies No - 05 Skills • Strong knowledge of pharmacology and medication safety • Good communication skills for patient education • Ability to manage pharmacy operations effectively About the Company • ECHS Gaya ensures access to safe and effective pharmaceutical services for ex-servicemen and their families through qualified pharmacists.How to Apply • Interested candidates should submit their applications to Station HQ, GayaStarting date08-01-2026Closing date05-02-2026Official NotificationClick Here

Role & Responsibilities • Process Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs). • Log and track Adverse Events (AE) and Serious Adverse Events (SAE). • Write patient narratives and code events using MedDRA. • Support safety report submissions and maintain safety databases. • Assist in quality review, reconciliation, and audit readiness. • Train and mentor junior staff.Qualifications & Experience • PharmD, MS/MA in Life Sciences, or BS/BA in related fields. • 1-2 years of experience in safety, pharmacovigilance, or clinical research.Skills • Knowledge of AE/SAE processing and safety databases. • Strong attention to detail and data accuracy. • Proficiency in MS Office and Windows.About the Company Fortrea is a global leader in clinical research and pharmacovigilance, providing safety and regulatory services to biopharmaceutical companies worldwide.

Role & Responsibilities • Collate data from primary/secondary data sources and maintain databases. • Interpret and analyze results using statistical techniques, providing summary reports. • Develop and implement data collection systems, analytics, and strategies for operational efficiency. • Work with cross-functional teams to gather data requirements for analysis projects. • Identify, analyze, and interpret trends or patterns in complex data sets. • Prepare dashboards for management meetings. • Identify opportunities for process improvement.Skills & Qualifications • Bachelor’s or Master’s degree in Pharmacy or Life Sciences. • 0-1 years of experience in data analysis, data cleaning, and validation (preferably from pharma/life sciences). • Experience with data visualization tools (Tableau, Power BI). • Technical expertise in data models, database design, data mining, and segmentation techniques. • Strong analytical skills with attention to detail and accuracy. • Ability to work both independently and collaboratively in a fast-paced environment. • Excellent communication skills.About the Company ClinChoice is a global leader in clinical research, offering comprehensive solutions to the pharmaceutical and life sciences industries. We focus on providing exceptional regulatory affairs services to support drug development and market authorization.