Browse the latest opportunities in Pharmacy Jobs.
About Role & Responsibilities • Monitor clinical trial sites for protocol compliance • Perform site initiation, monitoring and close-out visits • Ensure data quality and regulatory compliance • Coordinate with investigators and CRO teams • Maintain trial documentation and reports Qualification B.Pharm / M.Pharm / Pharm.D / MSc / BSc (Life Sciences) Experience 0 – 3 years Skills • GCP & ICH guidelines • Clinical monitoring • Documentation & reporting • Site coordination About the Company Thermo Fisher Scientific is a global leader in scientific services, clinical research and life-science solutions
About Role & Responsibilities • Review, assess and medically evaluate adverse event reports • Ensure accurate medical coding and causality assessment • Provide medical oversight for ICSR processing and signal detection • Support aggregate safety reporting and regulatory submissions • Participate in safety governance and risk management activities • Liaise with regulatory authorities and global stakeholders Qualification MBBS / MD Experience Minimum 5+ years in pharmacovigilance or clinical safety Skills • ICSR processing • Medical review & causality assessment • Aggregate safety reports (PSUR, PBRER, RMP) • Regulatory compliance • Excellent documentation and communication skills About the Company Indegene is a global healthcare solutions company providing technology-driven services across medical, regulatory and safety domains to leading pharmaceutical and life-science companies worldwide
About Role & Responsibilities • Oversee and manage the clinical pharmacy services within the hospital • Lead a team of clinical pharmacists to provide optimal pharmaceutical care • Ensure appropriate medication management and monitoring for patients • Collaborate with medical teams to recommend therapeutic strategies • Stay updated with the latest developments in pharmaceutical care and integrate them into practice • Provide educational support to staff and patients regarding medication use Qualification • Pharm.D or Ph.D. in Pharmacy • Board Certification or equivalent professional qualifications in Clinical Pharmacy Experience • 5+ years of experience in clinical pharmacy, with at least 3 years in a leadership role Skills • Strong leadership and team management skills • Excellent knowledge of pharmacotherapy and patient care • Ability to work effectively in a multidisciplinary healthcare environment About the Company King Faisal Specialist Hospital is a world-class healthcare institution in Riyadh, providing advanced medical services across various specialties
About the role & responsibilities • Dispense medications accurately and provide patient counselling • Advise on drug interactions, side effects and correct dosage • Manage pharmacy inventory and maintain records • Provide excellent customer service and patient care • Collaborate with healthcare professionals for optimal outcomes • Stay updated with pharmaceutical developments • Support and guide pharmacy technicians and staff Qualification • Bachelor of Pharmacy or equivalent • General AHPRA registration Experience • Freshers and experienced pharmacists welcome Skills • Strong medication knowledge • Excellent communication and interpersonal skills • High attention to detail and accuracy • Teamwork and problem-solving ability • Ability to work in a fast-paced environment About the company • Robina Good Price Pharmacy Warehouse is part of the Douglas Chemists Group delivering community-focused healthcare
About the role & responsibilities • Deliver dispensary pharmacy services and coordinate dispensary operations • Provide clinical pharmacy services across hospital units • Supervise pharmacy technicians, interns and students • Contribute to development of new pharmacy programs and services • Support accreditation and NSQHS compliance • Provide medication education to patients and healthcare teams • Participate in staff training and development activities Qualification • Bachelor of Pharmacy (or equivalent) • Current AHPRA registration Experience • Hospital or clinical pharmacy experience preferred Skills • Clinical pharmacy knowledge • Strong communication and teamwork • Time management and adaptability • Patient-focused approach • Ability to work flexible shifts including weekends About the company • Latrobe Regional Health is a leading regional health service delivering high-quality patient care
About the role & responsibilities • Perform triage and validity assessment of adverse event reports • Enter and process ICSRs in global safety databases • Assess cases for expedited reporting timelines • Prepare CIOMS, MedWatch and XML safety reports • Draft follow-up queries to obtain missing case information • Retrieve and review EVWEB cases • Maintain audit-ready safety documentation • Support additional pharmacovigilance activities Qualification • B.Pharm / M.Pharm • BDS • Life Science graduate Experience • Freshers and early-career candidates eligible Skills • Pharmacovigilance and ICSR processing knowledge • Strong communication skills • High attention to detail • Ability to meet regulatory timelines About the company • Cencora (PharmaLex India Private Limited) is a global healthcare services organization focused on drug safety and regulatory compliance
About the role & responsibilities • Act as CTMS subject matter expert and support system upgrades and user queries • Develop and maintain CTMS training materials and training matrix • Manage global trial disclosures and ensure regulatory compliance • Maintain eTMF systems as per DIA reference model and SOPs • Support LMS coordination and training documentation • Contribute to SOP review and quality compliance activities • Create dashboards and analytics using Power BI and BI tools • Perform data integrity and validation checks • Coordinate with internal and external stakeholders Qualification • Master’s in Science / Computers / Advanced Data Analytics • Equivalent industry experience accepted Experience • Minimum 5 years in pharma, IT software or data analytics domain Skills • CTMS, eTMF and Trial Disclosure management • Dashboard and BI analytics • SOP and compliance knowledge • MS Excel and MS Word proficiency • Strong documentation and multitasking skills About the company • Abbott Leading global pharmaceutical organization
About the role & responsibilities • Provide on-site clinical education and product training to healthcare professionals • Support surgeons during procedures and provide case coverage • Act as technical expert for assigned surgical and medical device products • Assist sales teams in territory planning and execution • Support clinical workshops, CMEs and conferences • Identify growth opportunities with regional sales and clinical teams • Coordinate closely with clinical leads and sales managers Qualification • B.Sc / B.Pharm / B.Tech Biomedical / Life Sciences Experience • 0 years • Freshers eligible Skills • Clinical and surgical technology interest • Strong communication and interpersonal skills • Willingness to travel for case support • Ability to work with sales and clinical teams About the company • Medtronic is a global leader in healthcare technology focused on life-saving innovations
About the role & responsibilities • Maintain complete and inspection-ready TMF • Review and approve TMF documents for quality and compliance • Manage version control and document consistency • Maintain eTMF system structure and health • Act as TMF point of contact during audits and inspections • Coordinate with CRAs for TMF updates • Conduct TMF gap analysis and process improvements Qualification • Bachelor’s / Master’s in Pharmacy, Life Sciences, Biology, Chemistry, Nursing or Public Health • PG Diploma in Clinical Research accepted Experience • 0–2 years • Freshers eligible Skills • eTMF management • Regulatory documentation knowledge • Audit and inspection readiness • MS Office and documentation tools • Strong communication skills About the company • Sun Pharmaceutical Industries Ltd is India’s largest pharmaceutical company with global operations
About the role & responsibilities • Maintain study documents including protocols, ICFs, CRFs and reports • Organize electronic and paper trial master files • Coordinate meetings, travel arrangements and minutes • Support regulatory document preparation and submissions • Ensure compliance with GCP and regulatory standards • Track site invoices and payments • Manage vendor code generation and vendor tracking Qualification • Bachelor’s / Master’s in Pharmacy, Life Sciences, Biology, Chemistry, Nursing or Public Health • PG Diploma in Clinical Research accepted Experience • 0–2 years • Freshers eligible Skills • Clinical documentation management • GCP and regulatory compliance knowledge • MS Office proficiency • Coordination and communication skills • High attention to detail About the company • Sun Pharmaceutical Industries Ltd is India’s largest pharmaceutical company with global operations
About the role & responsibilities • Execute global Pharmacovigilance audit programs • Conduct audits of CROs, vendors, affiliates and internal PV sites • Manage IAOD and track CAPA closures and deviations • Review and prepare Pharmacovigilance SOPs • Support corporate and regulatory inspections • Maintain LMS training documentation • Prepare monthly quality and compliance reports • Ensure adherence to global PV quality systems Qualification • M.Pharm • BDS Experience • 2+ years in Pharmacovigilance QA, PSUR or Signal Management Skills • Pharmacovigilance auditing • Global PV regulations and quality systems • Documentation and compliance management • Strong English communication • Cross-functional coordination About the company • Sun Pharmaceutical Industries Ltd is India’s largest pharmaceutical company with global presence
About the role & responsibilities • Act as subject matter expert for Clinical Data Management across global clinical trials • Review clinical protocols, CRF design, CDASH and CDISC compliance • Lead database design, edit checks, listings, dashboards and reconciliation plans • Manage CDM project timelines, deliverables, budgets and client coordination • Ensure SOP, GCDMP and regulatory compliance across studies • Maintain audit-ready TMF and CDM documentation • Mentor CDM teams and develop training and best-practice materials • Drive process improvement, SOP updates and adoption of new CDM technologies Qualification • Graduate degree in Life Sciences / Pharmacy / Biotechnology / Clinical Sciences Experience • 8+ years in Clinical Data Management • Minimum 4 years in a Senior CDM role in CRO or pharma Skills • EDC systems and database validation • CDISC standards (CDASH, SDTM) • Data reconciliation and inspection readiness • TMF, GCDMP and regulatory compliance • Client and stakeholder management • Team leadership and mentoring About the company • Novotech is a leading global CRO delivering end-to-end clinical trial services across multiple therapeutic areas
Join a leading tertiary care hospital. Responsibilities include medication therapy management. **Key Responsibilities:** - Provide high-quality patient care. - Collaborate with cross-functional teams. - Ensure compliance with medical standards. - Maintain accurate patient records. **About the Role:** This is a key position within our growing team. We offer competitive compensation and opportunities for professional development.
About the role & responsibilities • Execute Medical Affairs Plans for pre-launch and newly launched products • Engage in scientific exchange with healthcare professionals, key opinion leaders and ecosystem stakeholders • Provide scientific, clinical and pharmaco-economic information to HCPs • Develop and maintain peer-level scientific relationships • Conduct advisory boards, symposiums, MSL events, scientific exchanges and educational programs • Support evidence generation, investigator-initiated studies and publications • Gather medical insights on disease trends, patient pathways and treatment gaps • Support pharmacovigilance activities and adverse event reporting • Maintain compliance with ethical standards, GCP and regulatory guidelines • Deliver scientific training and presentations to internal and external stakeholders Qualification • Master’s degree in a scientific discipline • Doctoral degree preferred (MD / PhD / PharmD) Experience • Experience in pharmaceutical industry, medical affairs or clinical research preferred • Exposure to therapeutic area and KOL engagement Skills • Strong scientific communication and presentation skills • Stakeholder engagement and relationship management • Project management and analytical thinking • Knowledge of pharmacovigilance and GxP standards • Digital and technology-enabled scientific engagement About the company • AstraZeneca is a global science-led biopharmaceutical company focused on developing innovative medicines for serious diseases worldwide
Join a leading tertiary care hospital. Responsibilities include medication therapy management. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
Join a leading tertiary care hospital. Responsibilities include medication therapy management. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
Join a leading tertiary care hospital. Responsibilities include medication therapy management. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
Join a leading tertiary care hospital. Responsibilities include medication therapy management. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
About the role & responsibilities • Perform triage and case validity assessment of adverse event reports • Execute MedDRA and WHO-DD coding • Conduct duplicate checks and quality control of safety cases • Ensure compliance with ICH-GCP, 21 CFR Part 11 and global PV regulations • Maintain audit-ready safety data within digital PV systems • Provide subject matter expertise to improve safety platform workflows • Support reconciliation and safety data reviews Qualification • PharmD (mandatory) Experience • 0 – 4 years Skills • MedDRA & WHO-DD coding • Case validity & triage • Pharmacovigilance compliance • Data quality control • Microsoft Excel & Word About the company • CoReason.ai is a fast-growing HealthTech company building advanced analytics platforms for life sciences and healthcare organizations
About the role & responsibilities • Support development and execution of global PV audit programs • Conduct audits for CROs, vendors, affiliates and internal PV sites • Manage audit observation database and CAPA tracking • Review and update pharmacovigilance SOPs • Support corporate and regulatory inspections • Maintain training and LMS records • Prepare monthly quality and compliance reports • Ensure adherence to global PV quality systems Qualification • M.Pharm • OR BDS Experience • Minimum 2 years experience in PV Quality Assurance • OR PSUR preparation / Signal Management Skills • PV auditing & compliance • CAPA management • SOP documentation • Regulatory PV knowledge • Communication & coordination skills About the company • Sun Pharmaceutical Industries Ltd is India’s largest pharmaceutical company with global operations and strong focus on quality and innovation