Pharmacy Jobs

Roles & Responsibilities: Analytical Development Laboratory (ADL): • Perform routine analysis and analytical method development for solid orals, injectables, semi-solids, liquids, oral liquids, and APIs. • Execute analytical method validation, verification, and transfer including protocol and report preparation. • Independently handle HPLC, UV Spectrophotometer, and dissolution apparatus for assay, content uniformity, blend uniformity, dissolution, and related substances testing. Formulation & Development (F&D): • Develop formulations for solids, semi-solids, injectables, and oral liquids. • Conduct product development, stability studies, and scale-up activities in a GMP environment. • Support technology transfer and process optimization. Packaging Development: • Perform packaging material selection, development, and testing for pharmaceutical products. • Ensure packaging compliance with regulatory requirements for different dosage forms. • Support stability, compatibility, and packaging validation activities. Qualification: • ADL: M.Sc / B.Pharm / M.Pharm • F&D: M.Pharm • Packaging Development: B.Pharm / M.Pharm (Diploma/Certification preferred) Experience: • For ADL: 2–12 years • For F&D: 3–10 years • For Packaging Development: 3–10 years Skills: • Strong knowledge of GMP, analytical techniques, and pharmaceutical development processes. • Hands-on experience in formulation, analytical validation, or packaging development. • Good documentation, compliance, and cross-functional coordination skills.Walk-In Interview Details: Date: 1st February 2026 (Sunday) Time: 9:00 AM – 3:00 PM Venue: LINCOLN HOUSE, Behind Satyam Complex, Science City Road, Sola, Ahmedabad – 380060, Gujarat Documents to Carry: • Updated resume • Educational certificates • Experience letters • Relevant supporting documents About the Organization: Lincoln Pharmaceuticals Ltd is a WHO-GMP and ISO-certified pharmaceutical company based in Ahmedabad, focused on delivering affordable and innovative healthcare solutions with a strong presence across domestic and international markets.

Roles & Responsibilities: • Coordinate with Sponsors and internal Operations teams for clinical trial feasibility with quick turnaround times. • Oversee ethical conduct of Phase II–IV clinical trials in compliance with ICH-GCP and regulatory standards. • Ensure timely completion of clinical trials with high-quality, error-free data collection from sites. • Drive repeat business from Sponsors/CROs through superior site performance and delivery. • Train and mentor operations teams on essential clinical trial documents and ethical trial conduct. • Lead recruitment, capacity building, and performance development of the clinical operations team. • Handhold teams throughout the entire clinical trial lifecycle and identify high performers for vertical growth. • Prepare sites for FDA audits and ensure audit readiness. • Develop new clinical trial sites across India, including non-metro locations, and build therapeutic area–specific investigator networks. • Establish and implement SOPs, operational systems, controls, and efficient marketing processes. • Prepare business plans, achieve targets, and continuously improve operational and marketing strategies. • Anticipate risks, mitigate issues proactively, and ensure adherence to sponsor timelines. • Monitor market trends, gather industry intelligence, and keep management informed. • Prepare MIS and management reports and maintain strict control on headcount. Qualification: • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or related field. Experience: • Extensive experience in clinical operations with strong exposure to Phase II–IV clinical trials and site management. Skills: • Strong leadership and team-building capabilities. • Excellent sponsor and stakeholder management skills. • Deep understanding of clinical trial operations, ethics, and regulatory compliance. • Strategic planning, risk management, and business development skills. • Ability to work across metro and non-metro clinical trial sites. • Strong communication, training, and reporting skills. About the Organization: The organization operates in the clinical research domain with a focus on ethical, high-quality clinical trial execution across India. It emphasizes operational excellence, regulatory compliance, strong investigator networks, and sustainable growth through robust systems, processes, and team development.

Roles & Responsibilities: • Perform method validation and method verification for drug substance (DS), drug product (DP), and in-process samples. • Conduct stability studies, IRS qualification, and biosimilarity assessments. • Prepare and review controlled documents including specifications, STPs, SOPs, TDS, COAs, MVPs/MVRs, and MTRs. • Coordinate with vendors for external calibration and support in-house calibration activities. • Manage validation lab inventory, chemicals, standards, kits, and consumables. • Maintain laboratory instruments, equipment, and usage logbooks. • Conduct analyst qualification and training for validation lab team members. • Initiate and track QMS activities, deviations, and investigations. • Ensure cGMP compliance and adherence to laboratory safety requirements. • Support additional tasks assigned by the reporting manager. Qualification: • M.Sc / M.Pharm / Master’s degree in Biotechnology or related life science disciplines. Experience: • 2–5 years of hands-on experience in analytical validation laboratories (biologics/biosimilars preferred). Skills: • Strong hands-on experience with CEX-HPLC, SE-HPLC, ELISA, RT-PCR (HCDNA), Maurice, SOLO VPE. • Experience in HCP analysis, peptide mapping, glycan analysis, and capillary electrophoresis. • Knowledge of stability studies, method validation, and biosimilarity testing. • Sound understanding of cGMP, QMS, and laboratory compliance requirements. • Strong documentation, coordination, and analytical skills. About the Organization: Enzene Biosciences is a biopharmaceutical company focused on the development and manufacturing of biologics and biosimilars for global markets. With advanced analytical and validation laboratories, Enzene offers professionals the opportunity to work with cutting-edge technologies while building expertise in GMP-regulated biopharmaceutical quality and validation operations.

Roles & Responsibilities: • Lead authoring and review of aggregate safety reports (PSUR/PBRER, DSUR, PADER, Annual Reports). • Prepare benefit–risk evaluations, signal detection reports, and ad hoc regulatory safety documents. • Author and review RMPs, safety update reports, addendum reports, and CTD summaries (Clinical & Non-Clinical Overviews, Clinical Summaries). • Develop and update product labeling documents (CDS, USPI, SmPC/SPC, Medication Guides). • Conduct scientific literature reviews, recommend label updates, and prepare justification documents. • Generate and review line listings, summary tabulations, CFIs, and CFCs. • Prepare medical information responses for healthcare professionals (HCPs). • Coordinate safety writing projects including resource planning, timelines, and cross-functional communication. • Act as primary client contact for safety writing deliverables and ensure quality, compliance, and audit readiness. • Support RFPs, resource estimation, metrics tracking, and mentor junior writers. Qualification: • Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related field (Master’s/PhD preferred). Experience: • 5–7 years of experience in the pharmaceutical industry or minimum 4 years in medical/safety writing. Skills: • Strong expertise in pharmacovigilance regulations, ICH guidelines, and aggregate safety reporting. • Excellent scientific writing and communication skills. • Proficiency in MS Office and strong project coordination abilities. • Client-facing, leadership, and mentoring skills. • In-depth understanding of disease areas, drug safety lifecycle, and risk management. About the Organization: Fortrea is a global clinical development and pharmacovigilance services company supporting pharmaceutical and biotech organizations worldwide. With a strong focus on scientific excellence, regulatory compliance, and patient safety, Fortrea offers professionals the opportunity to lead complex global safety projects in a collaborative and growth-driven environment.

Roles & Responsibilities: • Perform routine sampling and physical/chemical analysis of raw materials, in-process samples, and finished products. • Conduct analytical tests such as pH, viscosity, solubility, and bulk density. • Operate laboratory instruments including UV-spectrophotometers and pH meters. • Prepare and maintain STPs, batch analysis reports, and laboratory documentation. • Support Out-of-Specification (OOS) investigations and implement CAPA. • Assist in formulation development of tablets, capsules, powders, and gummies. • Conduct lab-scale trials and sensory evaluations (taste, texture, aroma). • Coordinate with regulatory teams for FSSAI and AYUSH label compliance. • Perform stability and shelf-life studies for new formulations. Qualification: • B.Sc / M.Sc in Chemistry, Biochemistry, Food Science. • B.Pharm or M.Pharm. Experience: • 1–4 years of experience in nutraceutical or pharmaceutical manufacturing. Skills: • Working knowledge of FSSAI, GMP, and GLP regulations. • Strong understanding of analytical chemistry and QC testing. • Familiarity with bioactive compounds and herbal extracts. • High attention to detail and strong documentation skills. • Ability to collaborate effectively with Production, QA, and R&D teams. About the Organization: Immunosciences is a growing healthcare and nutraceutical organization focused on developing high-quality, compliant, and innovative supplement products. With integrated manufacturing and R&D capabilities, the company emphasizes quality assurance, regulatory compliance, and product innovation to meet evolving consumer and healthcare needs.

Roles & Responsibilities: • Support acquisition, validation, and standardization of structured and unstructured data. • Assist in maintaining data quality, integrity, and compliance with governance standards. • Apply company policies and procedures to routine data management activities. • Support analytics platforms, reporting systems, and data lifecycle processes. • Work on standard assignments involving basic analysis and problem-solving. • Refer to established policies, procedures, and best practices for guidance. • Escalate complex or unusual data issues to supervisors or senior team members. • Contribute to regulatory and business data compliance initiatives. Qualification: • Bachelor’s degree in Data, Analytics, IT, Life Sciences, Pharmacy, or a related field (or equivalent practical experience). Experience: • 0–1 year of experience; freshers are encouraged to apply. Skills: • Basic understanding of data management concepts and data governance frameworks. • Ability to follow standard operating procedures and guidelines. • Good communication and collaboration skills. • Attention to detail and willingness to learn enterprise data processes. • Basic analytical and problem-solving abilities. About the Organization: Cardinal Health is a global healthcare services and data-driven solutions company that supports hospitals, pharmacies, manufacturers, and healthcare providers worldwide. With a strong focus on trusted data, analytics, and regulatory compliance, Cardinal Health enables better healthcare outcomes while offering inclusive, growth-oriented career opportunities for early-career professionals and diverse talent.

Roles & Responsibilities: • Design and configure clinical databases using EDC systems such as Oracle Clinical and Medidata Rave. • Develop Case Report Forms (CRFs) aligned with formulation-specific clinical endpoints. • Perform data cleaning and query management, resolving discrepancies with clinical sites. • Conduct User Acceptance Testing (UAT) to validate database logic and edit checks. • Ensure data accuracy, consistency, integrity, and traceability throughout the clinical study lifecycle. • Support database lock activities and clinical data transfer to biostatistics teams. • Provide submission-ready clinical data to support global regulatory filings and formulation performance evaluation. • Collaborate with clinical, formulation R&D, and regulatory teams to ensure compliant data management practices. Qualification: • M.Pharm (Clinical) – Mandatory. Experience: • 2–5 years of experience in Clinical Data Management or Clinical R&D. Skills: • Hands-on experience with EDC systems (Oracle Clinical, Medidata Rave, or equivalent). • Strong understanding of GCP guidelines and clinical trial workflows. • Working knowledge of CDISC standards (SDTM/ADaM) preferred. • Excellent communication and cross-functional coordination skills. • Strong attention to detail and data quality mindset. About the Organization: Bachwell Pharma is a growing pharmaceutical company with a strong focus on formulation R&D for global regulatory markets. The organization supports development of tablets, injectables, and topical formulations, offering professionals the opportunity to work at the intersection of clinical research, data management, and regulatory submissions in a dynamic R&D environment.

Roles & Responsibilities: • Coordinate and support site-level clinical trial operations. • Act as a liaison between investigators, sponsors, CROs, and internal teams. • Track study timelines, milestones, and deliverables to ensure on-time execution. • Ensure compliance with ICH-GCP, SOPs, and applicable regulatory requirements. • Support study start-up, ongoing trial management, and close-out activities. • Maintain accurate and complete clinical trial documentation and reports. • Assist in monitoring site performance and resolving operational challenges. • Support audits, inspections, and quality improvement initiatives. Qualification: • Bachelor’s or Master’s degree in Life Sciences, Medical Sciences, Pharmacy, or related field. Experience: • 3–4 years of experience as a Project Coordinator or Project Manager in Clinical Research. Skills: • Strong understanding of clinical operations and site management. • Excellent communication, coordination, and leadership skills. • High attention to detail and strong organizational abilities. • Ability to manage multiple activities and stakeholders effectively. • Commitment to research quality, compliance, and ethical standards. About the Organization: The organization is a growing clinical research organization focused on delivering high-quality clinical trial execution through strong site-level operations and regulatory compliance. It offers professionals an opportunity to work in a dynamic environment, collaborate with cross-functional stakeholders, and contribute to impactful clinical research projects.

Roles & Responsibilities: • Perform daily website review and pharmacovigilance compliance monitoring for Europe, UK, WHO, and ROW markets (India, Kazakhstan, South Africa, Ukraine, etc.). • Identify safety-related updates and share with relevant stakeholders: ICSR updates with Case Processing team, PSUR updates with PSUR team, and signal-related updates with Signal Management team. • Draft, review, and update SOPs in line with evolving global pharmacovigilance regulations. • Coordinate with QPPV and Local Responsible Persons (LRPs) for regulatory queries and training activities. • Archive emails and documents as per pharmacovigilance compliance requirements. • Collect safety data from cross-functional teams for compliance report preparation. • Prepare, review, and circulate compliance reports as per approved templates and SOPs. • Conduct and support compliance meetings with QPPV, draft Minutes of Meeting (MoM), and track action items. Qualification: • M.Pharm in Pharmacology or Pharmaceutics. Experience: • 1–2 years of hands-on experience in Pharmacovigilance compliance, website review, and global regulatory reporting. Skills: • Strong knowledge of GVP Modules and global PV regulations (EU, UK, USFDA, India, MHRA, ROW). • Hands-on understanding of PSMF, ICSR, PSUR, and RMP. • Excellent written and verbal communication skills. • Strong documentation, time management, and coordination abilities. • Ability to work effectively in cross-functional pharmacovigilance teams. About the Organization: Macleods Pharmaceutical Ltd is a leading Indian pharmaceutical company with a strong global presence and a robust R&D focus. Known for its commitment to quality, compliance, and patient safety, Macleods operates across multiple regulated markets and offers professionals an opportunity to work on global pharmacovigilance systems in a dynamic and growth-oriented environment.

Roles & Responsibilities: • Lead and execute CMC regulatory strategies for post‑approval pharmaceutical products globally. • Prepare, review, and coordinate CMC documentation for post‑approval changes and lifecycle activities. • Assess scientific and technical data to evaluate regulatory impact and ensure risk-based, data-supported rationales. • Manage multiple CMC projects, ensuring timely, high-quality dossier submissions. • Collaborate with cross-functional teams (QA, QC, manufacturing, supply chain, packaging, device, analytics) and provide regulatory updates. • Translate complex technical concepts into clear regulatory justifications and influence cross-functional decisions. • Identify regulatory risks and opportunities and implement compliant solutions. • Participate in continuous improvement initiatives and maintain SOPs and internal guidelines. • Mentor junior colleagues and represent CMC regulatory function in project meetings. • Utilize MS Office and regulatory IT systems for efficient documentation management. Qualifications: • Bachelor’s or Master’s degree in Pharmacy, Science, or related field (advanced degree preferred). Experience: • 5-10 years of global Regulatory CMC experience. Skills: • Strong communication, regulatory strategy, and CMC documentation skills. • Cross-functional collaboration and stakeholder management. • Knowledge of pharmaceutical manufacturing, analytical testing, and quality systems. • Advanced MS Office and regulatory IT proficiency. • Leadership, mentoring, and project management abilities. About the Organization: Genpact is a global technology and professional services company that leverages deep industry expertise, advanced data, and AI-driven solutions to help enterprises transform and stay ahead. With a culture built on integrity, inclusion, and innovation, Genpact empowers over 140,000 professionals worldwide to solve complex business challenges, drive change, and deliver lasting value for clients across industries.

Roles & Responsibilities • Lead regulatory affairs for assigned franchise(s) from clinical development through lifecycle management • Develop and implement regulatory strategies, including risk mitigation and accelerated approval pathways • Drive SEC preparedness and support India’s inclusion in global clinical trials • Ensure 100% regulatory compliance, including post-approval commitments, labeling, site transfers, and biologics • Act as GRP Lead and ensure adherence to Good Regulatory Practices and quality management systems • Lead internal and external audits, ensuring deviations and CAPAs are addressed effectively • Collaborate cross-functionally with business, medical, QA, supply, and global regulatory teams • Support regulatory policy shaping, health authority advocacy, and industry association initiatives • Provide regulatory support to business development projects and oversee regulatory intelligence • Manage and develop regulatory team members (direct and indirect reports) Qualifications • Bachelor’s degree in Pharmacy (mandatory) • Post-graduate qualification in Pharmacy (preferred) Experience • Proven experience in regulatory affairs, drug development, and clinical trials • Prior people management and team leadership experience • Experience with innovative treatment modalities (desirable) Skills • Strong knowledge of Indian regulatory requirements • Strategic regulatory planning and risk management • Effective stakeholder management and cross-functional collaboration • Strong communication, leadership, and decision-making skills About the Organisation AstraZeneca is a global, science-led biopharmaceutical company focused on the discovery, development, and commercialization of innovative medicines. With a strong commitment to patient safety, scientific excellence, and ethical practices, AstraZeneca fosters an inclusive culture that encourages continuous learning, collaboration, and growth while advancing the future of healthcare worldwide.

Roles & Responsibilities • Perform medical and scientific data review for hematology clinical trials (e.g., myeloma, lymphoma) • Review standard data listings including adverse events, concomitant medications, efficacy and safety data • Conduct patient profile reviews, safety narratives, PD analysis, and scientific data evaluations • Support Lead Clinical Scientist and Medical Director in medical data review activities • Develop and contribute to Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans • Author medical data queries, review responses, and support query closure • Participate in medical and safety review meetings, including slide preparation • Collaborate with Clinical Operations, Data Management, Pharmacovigilance, and Project Management teams • Identify data trends, risks, and subject safety issues; escalate concerns appropriately • Ensure compliance with ICH-GCP, data privacy standards, SOPs, and regulatory requirements • Support audits and trusted process meetings as required Qualification • Degree in Life Sciences: MSc, PharmD, PhD, MD, DMD or equivalent Experience • Relevant scientific or clinical research experience in clinical development • Exposure to medical data review, clinical trials, or drug development preferred Skills • Strong understanding of clinical trial data, scientific principles, and ICH-GCP guidelines • Excellent analytical, documentation, and problem-solving skills • Strong written and verbal communication abilities • Proficiency in MS Office (Word, Excel, PowerPoint) • Ability to manage multiple tasks in a regulated, fast-paced environment • Strong collaboration and stakeholder management skills About the Organisation Syneos Health® is a leading global biopharmaceutical solutions organization, supporting clinical development, medical affairs, and commercialization. With operations across 110+ countries and involvement in the majority of novel FDA and EMA approvals, Syneos Health partners with customers to accelerate the delivery of therapies that improve and save lives worldwide.

Roles & Responsibilities • Monitor adherence to prescribed dose status across global clinical trial sites • Identify dose discrepancies and drive timely, traceable follow-ups with sites • Document dose-related risks and maintain inspection-ready records • Conduct routine and ad-hoc dose surveillance reviews as per protocol • Collaborate with Trial Managers, Clinical Medical Managers, and Medical Advisors • Support site engagement through clear communication and data insights • Coach site staff on dose compliance, documentation quality, and protocol adherence • Communicate findings to trial teams and contribute to continuous improvement initiatives Qualification • Graduate degree in Life Sciences: M.Pharm, PharmD, Pharmacy, BDS/MDS, or MSc Nursing Experience • Minimum 2 years’ experience in clinical trials (Pharma/Biotech/CRO/Hospital) • Exposure to global clinical operations and trial systems Skills • Strong understanding of ICH-GCP and clinical trial conduct • Analytical mindset with ability to interpret clinical data • Excellent communication and stakeholder management skills • Ability to work independently in dynamic environments • Coaching and influencing skills with strong attention to detail About the Organisation Novo Nordisk is a global healthcare company with a strong legacy in clinical research and innovation. Through its Global Business Services in Bangalore, the company supports worldwide clinical development with advanced risk-based monitoring, data quality, and patient safety initiatives, contributing to high-quality and compliant clinical trials across the globe.

Roles & Responsibilities • Perform publishing and technical validation of regulatory submissions (eCTD/CTD/NEES/Paper) for the US market • Conduct final technical quality review of submission dossiers • Dispatch submissions to health authorities or affiliates as per regulatory timelines • Handle post-submission activities including acknowledgements, receipts, and metadata capture in RIM systems • Upload and manage health authority correspondence, commitments, and related documentation • Ensure compliance with ICH and FDA guidelines in a regulated, process-driven environment • Coordinate with internal stakeholders and ensure timely communication of submission status Qualification • Bachelor’s degree in Pharmacy, Medicine, Chemistry, or related Life Sciences discipline Experience • Relevant experience in Regulatory Affairs Operations / Regulatory Publishing within the pharmaceutical industry Skills • Strong knowledge of ICH and FDA guidelines (US market) • Hands-on experience with eCTD, CTD, NEES, and paper submissions • Expertise in publishing tools such as Liquent, DocuBridge, or similar systems • Advanced English communication skills • Good understanding of RIM systems and regulatory workflows • Time management, organizational, and multitasking skills • Attention to detail and quality-focused mindset • Flexibility to adapt in a fast-changing environment About the Organisation Genpact is a global advanced technology services and solutions company that helps leading enterprises drive digital transformation through data, technology, and AI. Known for its strong regulatory, life sciences, and operations expertise, Genpact supports global pharma companies with end-to-end regulatory and compliance solutions while fostering innovation and continuous growth.

Roles & Responsibilities • Support clinical data management activities across clinical trials • Assist in data collection, validation, cleaning, and processing as per protocols and SOPs • Ensure accuracy, consistency, and completeness of clinical trial data • Work with standard guidelines to resolve routine data-related issues • Maintain and update clinical databases using approved systems and tools • Collaborate with team members and report to direct supervisors on assigned tasks • Follow detailed instructions for daily activities and new assignments • Contribute as an individual team member within a defined scope of work • Support regulatory compliance and quality standards in clinical data services • Work in rotational shifts as per business requirements Qualification • Bachelor of Pharmacy / Master of Pharmacy / Master’s in Actuarial Science Experience • 1 to 3 years of relevant experience in clinical data management or related roles Skills • Clinical Data Management concepts • Data collection, validation, and processing • Understanding of clinical research and trials • Attention to detail and data accuracy • MS Office and clinical data systems • Basic understanding of regulatory guidelines • Good communication skills (English – Intermediate) • Ability to work in a team-based environment About the Organisation Accenture is a global professional services company with strong capabilities in digital, cloud, and security. With a presence in over 120 countries, Accenture supports leading life sciences organizations across R&D, clinical trials, regulatory services, and pharmacovigilance, helping them deliver better patient outcomes through data-driven solutions.

Roles & Responsibilities • Secure regulatory approvals for new products (NDA, LCM) within defined timelines • Manage product lifecycle activities including submissions, variations, and renewals • Prepare and review regulatory submission dossiers and application forms as per country-specific Health Authority requirements • Coordinate with distributors, affiliates, and health authorities to ensure regulatory compliance • Handle regulatory documentation for tenders and special submissions • Update and maintain regulatory information in Veeva Vault within agreed timelines • Support labeling development, review promotional materials, and ensure compliance with local regulations • Monitor regulatory environment changes and support post-approval regulatory activities Qualification • Post-Graduation or equivalent degree in Science Experience • Minimum 5+ years of experience in Regulatory Affairs within the pharmaceutical industry • At least 3 years of experience working in cross-functional, international or affiliate environments • Experience handling interactions with Health Authorities preferred Skills • Regulatory submissions and lifecycle management • Health Authority interactions • Regulatory documentation and compliance • Veeva Vault (Regulatory systems) • Project management and prioritization • Cross-functional collaboration and stakeholder management About the Organisation Novo Nordisk is a global healthcare company with over a century of experience in developing innovative treatments for chronic diseases. Driven by a strong patient-centric mission, the organization focuses on delivering high-quality, compliant, and sustainable healthcare solutions across international markets.

Roles & Responsibilities • Assist in dispensing medicines as per prescriptions under pharmacist supervision • Support pharmacists in daily pharmacy operations • Handle medicine storage, labeling, and inventory management • Ensure compliance with pharmacy regulations and safety standards • Provide basic medication-related information to customers • Maintain cleanliness and organization of the pharmacy area • Support documentation and record-keeping activities Qualification • Diploma in Pharmacy (D.Pharm) • Bachelor of Pharmacy (B.Pharm) • Doctor of Pharmacy (Pharm.D) Experience • Freshers or experienced candidates may apply (experience preferred) Skills • Basic knowledge of medicines and dosage forms • Good communication and customer-handling skills • Attention to detail and accuracy • Ability to work under supervision • Basic computer and billing knowledge About the Organisation The hiring pharmacy operates in the UAE and provides quality pharmaceutical services focused on patient safety, accuracy, and professional care. 📧 Interested candidates can send details to: asstpharmacyjobsuae@gmail.com

Roles & Responsibilities • Manage and process clinical trial data including collection, validation, and review • Perform routine clinical data management tasks as per SOPs and standard guidelines • Ensure accuracy, consistency, and integrity of clinical trial data • Resolve data queries under supervision and follow predefined processes • Support data storage, integration, and analysis activities • Collaborate with internal team members and report to the direct supervisor • Follow regulatory, quality, and compliance requirements • Work as an individual contributor within a defined scope • Be flexible to work in rotational shifts when required Qualification • Bachelor of Pharmacy / Master of Pharmacy / Master’s in Actuarial Science Experience • 1 to 3 years of experience in Clinical Data Management or Clinical Data Services Skills • Clinical Data Management fundamentals • Clinical trial data collection and validation • Understanding of CDM processes and workflows • Attention to detail and data accuracy • Basic knowledge of regulatory requirements • Proficiency in MS Office and clinical databases • Good communication skills About the Organisation Accenture is a leading global professional services company with capabilities across digital, cloud, data, AI, and security. With operations in over 120 countries, Accenture supports life sciences organizations through end-to-end solutions spanning clinical research, pharmacovigilance, regulatory services, and patient-centric innovations.

Roles & Responsibilities • Manage and process clinical trial data including collection, validation, and review • Perform routine clinical data management activities as per SOPs and guidelines • Ensure data accuracy, consistency, and integrity across clinical databases • Resolve data queries and support issue resolution under supervision • Work with clinical data systems and specialized CDM tools • Collaborate with team members and report progress to the direct supervisor • Follow regulatory, quality, and compliance requirements • Operate as an individual contributor within a defined scope of work • Be flexible to work in rotational shifts if required Qualification • Bachelor of Pharmacy / Master of Pharmacy / Master’s in Actuarial Science Experience • 1 to 3 years of experience in Clinical Data Management or Clinical Data Services Skills • Clinical Data Management fundamentals • Data collection, validation, and quality checks • Understanding of clinical trial processes • Familiarity with clinical data systems and databases • Attention to detail and analytical thinking • Basic knowledge of regulatory compliance • Good communication skills About the Organisation Accenture is a global professional services company with strong capabilities in digital, cloud, data, AI, and security. Serving clients in over 120 countries, Accenture supports organizations across industries through Strategy & Consulting, Technology, Operations, Industry X, and Song. Its Life Sciences R&D practice enables leading biopharma companies to improve patient outcomes by delivering high-quality clinical, pharmacovigilance, and regulatory solutions.