Pharmacy Jobs

Role & Responsibilities • Lead end-to-end clinical data management activities for assigned studies • Perform and oversee EDC UAT, edit check validation, and data listing reviews • Manage SAE and vendor reconciliations ensuring medical data consistency • Review CRF/eCRF design and completion guidelines • Lead database freeze and lock activities • Prepare metrics, CPT tracking, and data cleaning reports • Mentor junior CDAs and act as backup to Project Data Manager • Participate in audits, inspections, and client-facing meetings Qualification • Bachelor’s degree in Life Sciences, Pharmacy, Biological Sciences, or Healthcare-related fields Experience • 5+ years in Clinical Data Management Skills • Advanced Rave, Inform, Oracle Clinical • Leadership, mentoring, and client-facing communication • SAE reconciliation, vendor reconciliation • Metrics/CPT handling, DMW, SDQ, Pinnacle 21 • Strong regulatory compliance knowledge About the Company Syneos Health is a global biopharmaceutical solutions organization known for conducting large-scale, high-impact clinical trials and delivering world-class clinical data management and regulatory services.

Role & Responsibilities • Perform end-to-end clinical data management activities from study start-up to database lock • Conduct EDC UAT, edit check validation, and clinical data listing reviews • Manage queries, discrepancies, and SAE reconciliations • Perform vendor data reconciliation (Lab, ECG, PK/PD, IRT, IVRS) • Support CRF/eCRF design, review, and completion guideline preparation • Execute database freeze and lock activities • Prepare data cleaning and metrics reports • Participate in audits and client-facing discussions Qualification • Bachelor’s degree in Life Sciences, Pharmacy, Biological Sciences, or Healthcare-related fields Experience • 3–5 years in Clinical Data Management Skills • Rave, Inform, Oracle Clinical • SAE reconciliation, edit check validation, EDC UAT • Local and central lab data review • DMW, SDQ, Pinnacle 21 (preferred) • Strong documentation and communication skills About the Company Syneos Health is a leading global biopharmaceutical solutions organization delivering end-to-end clinical development and data management services across FDA and EMA regulated studies worldwide.

Role & Responsibilities • Conduct bioanalytical and clinical research studies • Ensure protocol and regulatory compliance • Analyze and document research data Qualification • MD / M.Pharm / M.Sc Experience • 2–6 years Skills • Research methods, documentation, compliance About the Company Cliantha Research is a leading global CRO in bioanalytical and clinical research.

Role & Responsibilities • Prepare protocols, CSRs, and regulatory documents • Ensure compliance with ICH-GCP guidelines • Coordinate reviews and submissions Qualification • B.Pharm / M.Pharm / Pharm.D / M.Sc Life Sciences Experience • 1–2 years in medical writing Skills • Scientific writing, regulatory knowledge, documentation About the Company Cliantha Research is a reputed CRO delivering regulatory and medical writing services.

Role & Responsibilities • Lead data review and discrepancy management • Coordinate database lock activities • Mentor junior CDM staff • Ensure compliance with regulatory standards Qualification • B.Pharm / M.Pharm / Pharm.D / M.Sc Life Sciences Experience • 5–6 years in Clinical Data Management Skills • Advanced EDC handling, leadership, query management, documentation About the Company Cliantha Research is a global CRO offering clinical development, bioanalytical and regulatory services.

Role & Responsibilities • Validate and reconcile clinical trial data • Perform data cleaning and query resolution • Support database lock activities • Ensure compliance with CDM SOPs and GCP guidelines • Maintain study documentation Qualification • B.Pharm / M.Pharm / Pharm.D / M.Sc Life Sciences Experience • 3–5 years in Clinical Data Management Skills • EDC systems, data validation, GCP, attention to detail, MS Excel About the Company Cliantha Research is a global CRO providing end-to-end clinical research services supporting international clinical trials.

Role & Responsibilities • Perform medical review and approval of post-marketing ICSRs and clinical trial SAE reports • Assess seriousness, expectedness, causality and coding accuracy of safety cases • Prepare company medical comments, follow-up queries and similar event analysis • Complete and maintain safety trackers and supporting documentation • Support the Qualified Person for Pharmacovigilance in evaluation of safety issues • Review and provide medical input into periodic safety reports • Review literature screening strategies and evaluate articles for safety case identification • Contribute to medical evaluation of safety signals and ongoing risk assessment Qualification • MD (Doctor of Medicine) Experience • Open to Medical Doctors seeking entry or early-career growth in pharmacovigilance Skills • Strong understanding of pharmacovigilance principles and safety reporting • Ability to plan, organize, prioritize and manage multiple safety tasks • Excellent written and verbal English communication (minimum B2 level) • Strong presentation and documentation skills • Advanced proficiency in MS Office tools • Ability to work effectively across cultures and cross-functional teams About the Company PrimeVigilance is a global pharmacovigilance and regulatory affairs organization with operational presence across North America, Europe and Asia, supporting pharmaceutical and biotech companies with end-to-end drug safety, medical information and risk management services.

Role & Responsibilities • Author, manage and lead development of regulatory medical writing documents for global and domestic submissions • Prepare protocols, clinical study reports, investigator brochures, briefing documents, IND/NDA/MAA and regulatory response documents • Collect, evaluate and integrate cross-functional scientific data into showing cohesive submission strategies • Plan, outline, write, review, coordinate approvals and finalize regulatory documents • Conduct document initiation and comment-resolution meetings for stakeholder alignment • Ensure accuracy, consistency and scientific integrity across related documents • Perform quality checks, peer reviews and maintain audit-ready documentation • Coordinate scientific reviews and manage timelines and delivery risks • Maintain therapeutic area knowledge and regulatory guideline updates • Provide coaching, support metrics tracking and contribute to process improvements • Maintain training records and support vendor coordination when required Qualification • Doctoral or Post-Graduate degree in Life Sciences / Pharmacy or clinical degrees (MBBS / BDS / BAMS / BHMS etc.) • Advanced degree (MD / PhD) preferred Experience • Minimum 3+ years of experience in regulatory medical writing with leadership exposure Skills • Strong knowledge of ICH, global regulatory guidelines and pharma industry standards • Excellent scientific writing, documentation and editing skills • Strong project management, decision-making and risk-mitigation abilities • Excellent communication, stakeholder management and interpersonal skills • Innovative, detail-oriented and adaptable working approach About the Company Sun Pharmaceutical Industries Ltd (SPIL) is India’s largest pharmaceutical company and a leading global specialty generics organization with a strong R&D-driven culture delivering high-quality, affordable medicines across more than 100 countries.

Role & Responsibilities • Serve as primary interface between sponsors, vendors and internal Safety & PV teams • Provide line management to Safety and Pharmacovigilance associates and managers • Oversee operational delivery as per Safety Management Plans and contracted scope • Monitor quality, productivity and KPIs and resolve performance gaps • Lead PV projects and ensure timely safety reporting submissions • Review and approve study budgets, invoicing and financial forecasts • Act as escalation point for sponsors and provide regular project updates • Coordinate with Clinical, Data Management, Regulatory and other functions • Develop, review and approve SOPs, work instructions and process improvements • Support business development activities, proposals and bid defenses • Review safety sections of protocols, CRFs and SAE forms • Ensure compliance with ICH-GCP, GVP modules, global regulations and internal SOPs • Participate in audits, inspections, CAPA management and inspection readiness • Provide PV training and expert consultation to internal teams and clients Qualification • Bachelor’s degree in Life Sciences, Pharmacy, Nursing or related healthcare discipline Experience • Extensive leadership experience in Safety & Pharmacovigilance within CRO or global PV environments Skills • Strong knowledge of GVP, ICH guidelines and global safety regulations • Proven people management and project leadership abilities • Financial acumen for budget management and invoicing • Proficiency in MS Word, Excel, PowerPoint, Visio and Outlook • Excellent communication, stakeholder management and presentation skills • Ability to manage multiple priorities in a fast-paced, matrix environment About the Company Syneos Health® is a global biopharmaceutical solutions organization delivering integrated clinical development, medical affairs and commercial services, partnering with leading pharmaceutical companies worldwide to accelerate drug development and improve patient outcomes through innovation, quality and compliance.

Role & Responsibilities • Review clinical trial protocols and data review plans • Prepare and contribute to Data Quality Management Plans • Perform detailed review of clinical data listings and prioritize critical data • Manage query generation, resolution and data cleaning activities • Execute CRF freezing and database lock activities • Track and review external data loads including SAE, biomarker and adjudication data • Liaise with external vendors for discrepancy resolution • File essential documents in eTMF in line with master plan requirements • Ensure compliance with FDA, ICH and global data management standards • Train and mentor junior Clinical Data Management team members • Collaborate with cross-functional clinical teams to meet study timelines Qualification • Bachelor’s degree in Life Sciences, Pharmacy or related discipline Experience • Minimum 4 years of experience in clinical data review and management Skills • Strong knowledge of clinical drug development process • Hands-on experience with EDC systems (Medidata RAVE preferred) • Proficiency in Microsoft Office tools • Excellent written and verbal communication skills • Strong analytical, coordination and problem-solving abilities • Ability to work collaboratively in cross-functional environments About the Company Bristol Myers Squibb (BMS) is a global biopharmaceutical leader focused on discovering, developing and delivering innovative medicines that help patients prevail over serious diseases, offering professionals a collaborative, ethical and patient-centered work culture with strong career growth opportunities.

Role & Responsibilities • Coordinate day-to-day clinical trial activities at the site • Manage subject recruitment, screening and follow-up visits • Maintain source documents, essential trial files and study logs • Perform accurate data entry in EDC systems • Ensure compliance with study protocols, GCP and regulatory guidelines • Support investigators and clinical research teams during trial conduct • Assist during monitoring visits, audits and inspections • Ensure timely documentation and reporting Qualification • Degree or Diploma in Pharmacy, Life Sciences, Nursing or Allied Health Sciences Experience • Minimum 1 year of experience as a Clinical Research Coordinator Skills • Basic understanding of clinical research processes • Knowledge of GCP and ICH guidelines • Strong communication and coordination abilities • High attention to detail and data quality orientation • Effective documentation and time-management skills About the Company Canvass Clinical Research Services Pvt. Ltd. is a growing clinical research organization providing comprehensive site management and clinical trial coordination services, offering professionals hands-on exposure, structured learning and strong career growth opportunities in the clinical research domain.

About the Role Fresenius Kabi is expanding its Global Vigilance Medical Writing team and is hiring experienced Aggregate Medical Writers to support global safety surveillance, signal management, and regulatory compliance activities across multiple international markets. This is a high-impact pharmacovigilance medical writing position for professionals who specialize in aggregate safety report authoring and signal documentation and are seeking global exposure with a structured long-term growth pathway.Key Responsibilities Author and review aggregate safety reports including PSURs, PBRERs, RMPs, ACOs, and PADERs Develop signal evaluation narratives and safety strategy documentation Conduct systematic literature reviews to identify safety signals and emerging risks Ensure compliance with global pharmacovigilance regulations and internal SOPs Collaborate with safety physicians, PV operations teams, and regulatory stakeholders Support benefit-risk evaluations and regulatory submissions Maintain inspection-ready documentation and reporting standardsEligibility Criteria Education (Mandatory): PhD / PharmD / M.Pharm / BDS Experience: 4–9 years in pharmacovigilance medical writing Core Expertise: PSUR / PBRER / RMP / ACO / PADER authoring Signal evaluation & narrative writing Regulatory compliance & literature review Work Mode: On-site – Gurgaon (1-day flexi WFH)Why Fresenius Kabi? Global exposure to high-impact pharmacovigilance programs Career progression in one of the world’s most respected healthcare organizations Structured learning and professional development programs Collaborative global PV culture with inspection-ready processes Highly competitive compensation

Key Responsibilities Coordinate and monitor clinical trial activities from site start-up to close-out Perform on-site and remote monitoring visits in accordance with monitoring plans Conduct Risk-Based Quality Monitoring (RBQM), including SDV and SDR Review and manage data in EDC, CTMS, IWRS, and eTMF systems Ensure compliance with ICH-GCP, SOPs, and regulatory requirements Maintain audit readiness and support site audits and inspections Prepare monitoring visit reports and follow-up letters Track country-level site metrics and proactively resolve issues Maintain regular communication with investigators and site teams Support CAPA planning and implementation Mentor junior CRA team members when required Travel up to 60–75% as per monitoring plan Complete timesheets, expense reports, and other trial documentationEligibility Criteria Postgraduate degree in Life Sciences or related discipline Minimum 1–1.5 years of mandatory on-site monitoring experience Strong working knowledge of ICH-GCP and regulatory guidelines Experience in FSP model preferred Hands-on experience with EDC, CTMS, IWRS, and eTMF systems Valid driving license (where applicable) Excellent written and verbal communication skillsRequired Skills Stakeholder and site relationship management High attention to detail and documentation accuracy Ability to manage multiple studies simultaneously Strong problem-solving and risk mitigation capability Independent working with collaborative mindset Proficiency in MS Office and clinical trial softwareWhy Join CRG? Work on global trials across 100+ countries Exposure to Top-50 pharma and 750+ biotech sponsors Fully remote work model Clear career progression from CRA I to CRA II and senior levels Continuous training and mentoring programs Strong compliance-driven and quality-focused culture

Job Responsibilities • Dispense medications accurately and safely • Review prescriptions for appropriateness and patient safety • Counsel patients on correct medicine usage, dosage, and precautions • Maintain pharmacy inventory, stock levels, and documentation • Coordinate with doctors and nursing staff for medication clarification and continuity of careEligibility Criteria • B.Pharm degree (Mandatory) • State Pharmacy Council Registration (Required) • Freshers & Experienced candidates can applyPreferred Skills • Knowledge of hospital pharmacy operations • Good verbal communication skills • Willingness to work in rotational shifts

Role & Responsibilities • Lead and manage outpatient pharmacy operations as Pharmacy In-charge • Ensure full compliance with DHA, MOH and UAE pharmaceutical regulations • Develop, implement and monitor pharmacy policies, SOPs and professional standards • Supervise storage, preparation, dispensing and distribution of all medications • Secure permits and manage controlled, narcotic and psychotropic drug documentation • Maintain and update hospital drug formulary and evaluate new pharmaceutical products • Coordinate with vendors and pharmaceutical agents to ensure regulatory compliance • Serve as Co-Chairperson of Pharmacy & Therapeutics Committee • Monitor adverse drug reactions and act on MOH circulars and safety alerts • Train pharmacy staff on infection control, fire safety and professional practices • Prepare duty rosters, leave schedules and manpower planning Experience • 4 – 9 years of hospital/clinical pharmacy experience • Minimum 2 years in pharmacy administration or leadership role • Lead audits, quality improvement initiatives and staff orientation programs Qualification • Bachelor’s Degree in Pharmacy (B.Pharm / PharmD / M.Pharm) • Valid DHA License to practice in UAE • Current license in country of originSkills • Strong knowledge of DHA and MOH pharmaceutical regulations • Leadership and team management skills • Controlled drug and narcotics handling expertise • Vendor coordination and formulary management • Excellent communication in English (Arabic desirable) • Policy development and quality assurance capability About the Company NMC Healthcare LLC is one of the largest private healthcare providers in the UAE, delivering multispecialty medical services across hospitals, clinics and pharmacies. NMC is known for its commitment to patient safety, clinical excellence and regulatory compliance, serving a diverse international patient population.

Role & Responsibilities Liaise with doctors, nurses and healthcare teams for safe and effective drug therapy Dispense and clinically verify prescriptions and supplied medicines Ensure compliance with Medicines Ethics, hospital SOPs, safety and risk management protocols Manage controlled and narcotic drugs with proper documentation and regulatory adherence Prepare purchase orders (PO), GRN and handle purchase returns for near-expiry medicines Arrange non-available medicines from nearby chemists Conduct quarterly stocktaking and inventory monitoring Coordinate daily cash handover to cashier Qualification D.Pharm or B.Pharm Experience 1 – 7 years of relevant hospital/clinical pharmacy experience Skills Prescription dispensing and clinical verification Controlled drug and narcotics handling Inventory, PO/GRN and stock management Regulatory compliance and documentation Coordination and communication with healthcare teams About the Company A multi-speciality hospital based in Bangalore providing comprehensive inpatient and outpatient healthcare services

Role & Responsibilities Consolidate daily, weekly and monthly pharmacy KPIs Monitor near-expiry medicines, stock adjustments and inventory levels Address and document drug-related queries and medication issues Supervise OP and IP pharmacy operations and pharmacy store activities Develop and enforce pharmacy policies, SOPs and best practice protocols Schedule pharmacy staff duties, shifts and training programs Maintain hospital formulary, expiry control and controlled drug storage Manage prescriptions, execute supply and shipment orders Handle customer complaints, service issues and departmental coordination Present reports to GM and participate in monthly review meetings Qualification B.Pharm or D.Pharm Experience Minimum 8+ years in hospital pharmacy operations Prior experience in a pharmacy supervisory role mandatory Skills Hospital pharmacy supervision and inventory management KPI tracking, reporting and analytical skills Policy implementation and regulatory compliance knowledge Leadership, training and staff coordination Strong communication and problem-solving ability About the Role This position leads hospital pharmacy operations, ensuring KPI governance, safe medication practices, regulatory compliance and efficient OP/IP pharmacy management while supporting service quality and clinical coordination.

Role & Responsibilities Ensure pharmacy compliance with NABH standards, Drugs & Cosmetics Act and NDPS regulations Maintain SOPs, licenses and statutory pharmacy documentation Manage procurement, storage, FIFO, expiry control and emergency drug availability Oversee safe dispensing practices, LASA and high-risk medication protocols Conduct audits, RCA, CAPA and continuous quality improvement initiatives Supervise pharmacy staff, duty rosters, training and performance reviews Coordinate with clinicians, nurses and PTC for rational drug use and formulary management Monitor narcotic drug control, registers and reconciliation Prepare pharmacy budgets, control costs and minimize wastage Ensure accurate billing, insurance reconciliation and revenue tracking Supervise HIS-based pharmacy operations, e-prescriptions and barcode safety systems Qualification B.Pharm with M.Pharm or Master’s in Hospital Administration Experience Minimum 6+ years in hospital pharmacy operations At least 2 years in a supervisory or managerial role Skills NABH and regulatory compliance expertise Inventory, audit, budgeting and cost-control skills Leadership, training and staff management HIS/automation proficiency and analytical ability Multilingual communication: English, Kannada, Hindi, Tamil, Telugu About the Company Manipal Hospital, Mysore is a leading multi-specialty healthcare institution delivering comprehensive medical services with strong emphasis on NABH-compliant quality standards, patient safety and technology-enabled clinical excellence.

Role & Responsibilities Lead and manage overall pharmacy operations and staff Ensure compliance with state and federal pharmacy regulations and accreditation standards Oversee accurate dispensing, verification and inventory control of medications Implement pharmacy policies, SOPs and quality improvement initiatives Provide patient, family and clinician education on safe medication use Coordinate with medical teams for medication therapy management Manage pharmacy budgeting, procurement and expense control Maintain relationships with patients, vendors and regulatory bodies Qualification B.Pharm or M.Pharm Valid Pharmacist registration with State Pharmacy Council Certification in pharmacy management or healthcare administration preferred Experience Minimum 5+ years in hospital pharmacy management or in-charge role Skills Strong leadership and team management Knowledge of regulatory compliance and NABH/quality standards Proficiency in pharmacy management software and documentation Inventory, budgeting and financial control skills Excellent communication and problem-solving abilities About the Company Jeevandan Multispeciality Hospital is a growing healthcare institution based in Patna, Bihar, delivering comprehensive multi-specialty medical services. The hospital focuses on quality patient care, clinical excellence and continuous service improvement through structured hospital systems and modern healthcare practices.