Pharmacy Jobs

Roles & Responsibilities • Analyse drug development information from clinical trials, regulatory agencies, and scientific sources • Track new drugs, pipeline updates, development phases, indications, and sponsors • Perform primary and secondary research on global drug development activities • Summarize, edit, and validate scientific and pharmaceutical content with high accuracy • Conduct comprehensive online searches for drug and clinical intelligence • Maintain assigned production volumes, quality standards, and KPIs • Collaborate with global teams across regions and business units • Follow SOPs and contribute to process improvement initiatives • Adapt to workflow changes in a fast-paced research environment Qualification • M.Pharm / B.Pharm / D.Pharm Experience • Freshers or up to 6 months of relevant experience Skills • Strong understanding of drug development and clinical research concepts • Excellent written and verbal communication skills • Good content analysis, summarization, and editing abilities • Proficiency in MS Word, Excel, and PowerPoint • Strong attention to detail and time management skills • Exposure to AI tools for research or content analysis • Basic knowledge of SQL or Python • Interest in pharmaceutical analytics, clinical intelligence, and drug pipelines About the Team Clarivate’s Drug Development (CDDI) team delivers high-quality intelligence on clinical trials, regulatory pipelines, and drug research, covering MoA, development milestones, regulatory pathways, and disease focus to support global pharmaceutical decision-making.

Roles & Responsibilities Quality Assurance (Injectable / API) • Perform IPQA activities for injectable manufacturing • Review batch manufacturing and batch packing records • Ensure compliance with cGMP, SOPs, and regulatory guidelines • Support deviation handling, CAPA, and documentation • Assist in audits and regulatory inspections Production (Injectable) • Operate injectable manufacturing processes as per SOPs • Support activities related to filling, lyophilization, and packaging • Maintain production documentation and comply with safety guidelines • Follow cGMP and quality standards during manufacturing operations Qualification • M.Pharm / B.Pharm / M.Sc Experience • Freshers only Skills • Basic knowledge of injectable manufacturing processes • Understanding of cGMP, SOPs, and quality systems • Good documentation and compliance orientation • Willingness to work in shift-based manufacturing environments Walk-In Interview Details • Date: 24 January 2026 (Saturday) • Time: 10:00 AM to 04:00 PM • Venue: Gufic Biosciences Ltd, N.H. 48, Near GEB Grid, Kabilpore, Navsari, Gujarat – 396445 • Contact: +91 63599 21281 • Email for CV submission: binal.kapadia@guficbio.com • Documents to carry: Original degree certificate (provisional not accepted), updated resume, ID proof About the Organisation Gufic Biosciences Ltd is a leading pharmaceutical company specializing in lyophilized injectables and APIs, with multiple global regulatory accreditations including WHO GMP, EU GMP, and approvals across several international markets. The Navsari facility offers strong learning opportunities for freshers seeking careers in injectable manufacturing and quality assurance.

Roles & Responsibilities • Develop and validate bioanalytical methods using LC-MS/MS and HPLC • Perform sample analysis for Bioavailability/Bioequivalence (BA/BE) studies • Apply extraction techniques such as SPE and LLE for accurate quantitation • Operate, maintain, and calibrate laboratory instruments as per SOPs • Ensure compliance with GLP, GDP, and regulatory requirements • Perform quality control checks for method validation and BA/BE studies • Handle compliance observations, CAPA, and QA/RA review responses • Maintain calibration records, inventory, temperature logs, and lab documentation Qualification • M.Pharm or M.Sc Experience • 3 to 8 years of experience in bioanalytical or pharma R&D roles Skills • Hands-on expertise in LC-MS/MS and HPLC • Strong knowledge of bioanalytical method development and validation • Experience with BA/BE studies and regulatory guidelines (DCGI, USFDA) • Good documentation practices and compliance mindset • Attention to detail and strong analytical skills About the Organisation Torrent Pharmaceuticals Ltd is a leading Indian pharmaceutical company with strong R&D capabilities and a focus on innovation, quality, and regulatory excellence. Its Gandhinagar R&D Centre plays a key role in advancing bioanalytical research and supporting the company’s global product pipeline.

Roles & Responsibilities • Provide scientific and medical support for the GSM portfolio across Gulf countries • Ensure continuous scientific updates and medical input for cross-functional teams • Communicate scientific data on approved products and pipeline to scientific leaders • Support Policy & Access teams for formulary inclusion and reimbursement activities • Plan and execute scientific education programs to engage the GSM medical community • Conduct input-seeking activities to understand local epidemiology and treatment patterns • Deliver medical training to Commercial, Market Access, Sales, and Regulatory teams • Ensure all promotional and non-promotional activities comply with company SOPs, codes, and local/international regulations Clinical Research & Pharmacovigilance • Support global, regional, and local clinical research and data generation activities • Identify and support appropriate clinical trial sites and investigators • Ensure timely adverse event reporting and support pharmacovigilance activities Qualification • Physician or Pharmacist educational background Experience • 1 to 2 years of experience in Medical Affairs within a multinational pharmaceutical company • Immunology therapeutic area experience preferred Skills • Strong medical and scientific knowledge • Experience in medical communications and medical affairs strategy • Excellent communication and stakeholder engagement skills • Strategic thinking and project management abilities • Proficiency in Microsoft Word, PowerPoint, and Excel • Fluency in Arabic and English Additional Information • Relocation: Not available • VISA Sponsorship: Yes • Travel Requirements: None • Flexible Work Arrangements: As per company policy About the Organisation MSD (Merck Sharp & Dohme) is a global, research-driven biopharmaceutical company committed to using leading-edge science to save and improve lives worldwide. Through its General & Specialty Medicine portfolio, MSD continues to advance medical practice and address high unmet medical needs, striving to be the most trusted, science-driven Medical Affairs organization in the industry.

Roles & Responsibilities • Perform quality control testing for OSD formulations • Conduct analysis using HPLC, GC, and microbiology techniques • Ensure compliance with GLP, SOPs, and cGMP requirements • Maintain accurate QC documentation and analytical records • Support routine testing, investigations, and lab activities • Ensure data integrity and timely reporting of results Qualification • M.Pharmacy / B.Pharmacy / MSc Experience • 1 to 5 years of experience in Quality Control for OSD formulation Skills • Hands-on experience with HPLC and GC • Knowledge of GLP and microbiology testing • Strong documentation and compliance skills • Attention to detail and quality-focused mindset Walk-In Interview Details • Date: 24 January 2026 (Saturday) • Time: 09:00 AM to 01:00 PM • Venue: Sy. No. 261, Plot No. 13 to 14, Annaram (Village), Jinnaram, Hyderabad • Contact No. for Queries: 9121185330 • Documents to carry: Updated resume, academic documents, ID proof, passport-size photo, latest increment letter and payslips (if applicable) About the Organisation Annora Pharma Pvt Ltd is a pharmaceutical company specializing in OSD formulations, with a strong focus on quality, compliance, and regulatory standards. The organization offers growth-oriented opportunities for professionals passionate about pharmaceutical quality systems and laboratory excellence.

Role & Responsibilities • Provide scientific and medical support for AbbVie Oncology portfolio • Execute Medical Affairs strategy and initiatives in India • Engage Key Opinion Leaders (KOLs), physicians, and academic stakeholders • Deliver fair, balanced, and evidence-based scientific information • Conduct scientific education, presentations, and training programs • Support advisory boards, round tables, and medical meetings • Facilitate clinical research and investigator-initiated studies • Serve as internal medical/scientific expert for disease-state and product knowledge • Collaborate cross-functionally with Medical, Commercial, R&D, and Clinical teams • Document all medical activities accurately and on time • Maintain compliance with ethics, PV, regulatory, and company SOPs • Manage medical activities within assigned budget • Provide training to internal teams (medical, sales, cross-functional) • Travel extensively (~60%) for field medical engagementQualification • MD (Preferred) • MBBSExperience • 2–3 years post-qualification experience in Medical Affairs • Experience in pharma industry or clinical research preferred • Experience working in matrix and cross-functional environmentsSkills • Strong scientific and clinical knowledge in Oncology • Excellent presentation and communication skills • Ability to translate complex data into clear medical insights • Strong relationship-building with KOLs and stakeholders • Analytical ability to interpret clinical data • Training and teaching capability • Proficiency in MS Office and medical systems • Compliance-driven and ethical work approachAbout Company • AbbVie is a global research-based biopharmaceutical company • Focus areas include Immunology, Oncology, Neuroscience, and Eye Care

Roles & Responsibilities Production • Operate injectable manufacturing processes including autoclave, compounding, vial washing, tunnel, capping, filling, lyophilizer, manufacturing, and packing • Ensure adherence to SOPs, cGMP, and safety requirements • Support routine production activities and documentation Quality Assurance • Perform IPQA activities and review batch documentation • Support APQR, validation, QMS, and compliance activities • Ensure regulatory and cGMP compliance Qualification • M.Pharm / B.Pharm / M.Sc / B.Sc Experience • 2 to 12 years of relevant experience in injectable manufacturing, engineering, or quality assurance Skills • Knowledge of injectable manufacturing processes • Understanding of cGMP, SOPs, and quality systems • Experience with production equipment, utilities, or QA documentation • Strong compliance and documentation skills Walk-In Interview Details • Date: 25 January 2026 (Sunday) • Time: 09:00 AM to 03:00 PM • Venue: Four Points by Sheraton Vadodara, 1275 Ward No. 7, Fatehgunj, Vadodara, Gujarat – 390008 • Documents to carry: Updated resume, educational certificates, experience letters, and ID proof About the Organisation Zydus Lifesciences Limited is a global, innovation-driven pharmaceutical company with strong capabilities in injectable manufacturing, quality systems, and healthcare solutions. With a focus on quality, compliance, and patient-centric innovation, Zydus offers robust career opportunities across manufacturing, engineering, and quality functions.

Roles & Responsibilities Production • Perform parenteral manufacturing activities for vials, bags, ampoules/bottles and BFS technology • Follow production quality systems, packing compliances, and SOPs • Support investigations, remediation activities, and CCN/CAPA handling Quality Assurance (QA) • Handle IPQA activities, validation, and documentation • Support QMS, compliance, DQA, and audit readiness • Ensure adherence to cGMP and regulatory requirements for sterile and non-sterile dosage forms Quality Control (QC) • Perform testing for chemistry, microbiology, and instrumentation • Support routine analysis for sterile and non-sterile products • Maintain QC documentation and compliance Analytical Development Laboratory (ADL) • Perform analytical method development and validation • Conduct testing using HPLC, GC, dissolution, UV, TOC, and sterility testing • Support stability studies, documentation, and regulatory compliance Qualification • B.Sc / M.Sc / B.Pharm / M.Pharm or equivalent Experience • Freshers to 6 years of experience depending on role • ADL roles require 1 to 5 years of relevant hands-on experience Skills • Knowledge of parenteral manufacturing and sterile/non-sterile dosage forms • Understanding of cGMP, ICH guidelines, and regulatory standards • Experience with validation, IPQA, QMS, investigations, and CAPA • Analytical skills in chromatography and laboratory instrumentation • Strong documentation and compliance orientation Walk-In Interview Details • Date: January 30, 2026 (Friday) • Time: 08:00 AM to 11:00 AM • Venue: AcuLife Healthcare Private Limited, Near Railway Crossing, Sanand-Viramgam Highway, Village: Sachana, Taluka: Viramgam, District: Ahmedabad, Gujarat – 382150 (Formerly Nirlife) • Email for CV submission: recruitment@aculife.co.in/rajeshthtakor@aculife.co.in • Documents to carry: Updated resume, educational certificates, experience letters (if applicable), and ID proof About the Organisation AcuLife Healthcare Pvt Ltd, part of the reputed Nirma Group, is a leading pharmaceutical company specializing in infusions, injectables, critical care medicines, and other healthcare products. With a strong focus on quality, affordability, and innovation, AcuLife offers excellent learning and growth opportunities for freshers and experienced professionals in pharmaceutical manufacturing and quality functions.

Roles & Responsibilities • Create, update, and maintain records in the COA Accelerator (COAA) database • Review and verify Clinical Outcome Assessment (COA) data for accuracy and consistency • Ensure compliance with COAA SOPs, work instructions, and data integrity standards • Identify, document, and resolve data integrity and data quality issues • Maintain logs and documentation for data integrity assessments • Collaborate with clinical, data management, and analytics teams • Monitor clinical data systems for anomalies and escalate issues • Support data integrity training and awareness initiatives • Contribute to continuous improvement in data governance and data quality Qualification • Bachelor’s degree in Life Sciences (mandatory) Experience • Minimum 2 years of experience in clinical data management or Clinical Outcome Assessments (COA) Skills • Strong attention to detail and analytical mindset • Proficiency in Microsoft Excel • Good communication and teamwork skills • Knowledge of clinical trial data integrity principles • Experience with COA descriptions, scoring, and administration is a plus • Exposure to data visualization or information science methodologies is an advantage About the Organisation IQVIA is a global leader in clinical research and healthcare intelligence, enabling life sciences organizations to advance healthcare through data-driven insights and regulatory-compliant clinical research.

Roles & Responsibilities • Lead end-to-end study-level Clinical Data Management activities from start-up to database lock and closeout • Prepare and execute Data Management Plans, data cleaning strategies, and query workflows • Perform ongoing data review including clinical, lab, and third-party data reconciliation • Manage data management vendors, snapshots, interim analyses, and data migrations • Track KPIs, manage timelines, and identify operational risks • Ensure inspection readiness, audit support, and TMF compliance • Apply CDISC (SDTM, ADaM) and AstraZeneca data standards • Mentor junior CDM team members and support process improvements Qualification • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Clinical Research, Biotechnology, or related field Experience • Study-level Clinical Data Management experience in pharma, biotech, or CRO settings • Experience with global clinical trials, EDC systems, and third-party data • Exposure to database lock, audits, and regulatory inspections Skills • Strong EDC, query management, and data quality oversight expertise • Vendor management and operational metrics tracking • Knowledge of CDISC standards (SDTM, ADaM) • Strong cross-functional communication skills • Experience with complex trials or interim analyses is a plus About the Organisation AstraZeneca is a global biopharmaceutical company focused on innovative, science-led medicines. The Bangalore site supports global clinical development, offering opportunities to work on high-impact trials and grow within a world-class research organization.

Roles & Responsibilities • Implement global Risk-Based Monitoring (RBM) strategies, processes, and quality standards across clinical trials • Ensure full compliance with ICH-GCP guidelines, internal SOPs, and regulatory requirements • Collaborate with global study teams and stakeholders to meet study timelines and objectives • Provide technical expertise and clear, customer-focused communication within cross-functional teams • Configure, test, and maintain study-level RBM systems • Define, monitor, and manage Key Risk Indicators (KRIs) • Ensure RBM system alignment with study protocols and regulatory expectations • Perform centralized monitoring to assess data quality, completeness, and accuracy • Review RBM system outputs for signal detection and action management • Support issue resolution and follow up with clinical and data management teams • Maintain quality control documentation related to RBM activities • Partner with Clinical Data Scientists to mitigate risks and support RBM system releases Qualification • Bachelor’s degree or higher in Life Sciences, Pharmacy, Clinical Research, or a related discipline Experience • Minimum of 4 years of experience in clinical trials, such as CRA, Clinical Data Management, Programming, or Central Monitoring roles Skills • Strong understanding of clinical trial monitoring, RBM frameworks, and regulatory processes • Knowledge of Phase I–IV clinical development and study design principles • Experience with clinical trial data review, CRF design, database setup, and data cleaning • Familiarity with RBM tools and clinical trial databases • Technical exposure to Oracle, PL/SQL, SAS, Java, or relational databases • Proficiency in MS Office tools including Excel, Word, PowerPoint, and Project • Strong communication, analytical, and problem-solving skills • Ability to work independently and manage multiple priorities About the Company Pfizer is a global biopharmaceutical leader dedicated to discovering, developing, and delivering innovative medicines and vaccines that improve health worldwide. With a strong commitment to scientific excellence, patient safety, and regulatory compliance, Pfizer operates across the full spectrum of clinical development, offering professionals meaningful career growth and exposure to global clinical research programs.

Roles & Responsibilities • Conduct in-vitro ADME studies including solubility, stability, plasma protein binding, metabolic stability, drug–drug interaction studies, and Caco-2 permeability assays • Perform bioanalytical sample preparation and support LC-MS/MS data acquisition and integration • Record raw data accurately and perform data acquisition, compilation, analysis, and scientific interpretation • Ensure data integrity, accuracy, and compliance with SOPs and quality standards • Prepare study plans, protocols, and detailed study reports • Maintain laboratory instruments, equipment, and work areas as per approved SOPs • Execute assigned experimental work independently with minimal supervision • Follow laboratory safety, quality, and documentation practices consistently Qualification • Master’s degree in Pharmacy, Biotechnology, Chemistry, Biochemistry, or a related discipline Experience • 1–4 years of relevant experience in in-vitro ADME and bioanalytical studies Skills • Hands-on experience with in-vitro ADME assays • Practical knowledge of LC-MS/MS techniques • Strong understanding of bioanalytical sample preparation and data analysis • Knowledge of laboratory SOPs, GLP principles, and data integrity requirements • Strong analytical, documentation, and reporting skills • Ability to work independently with attention to detail About the Company Eurofins is a global leader in laboratory testing and bioanalytical services, supporting pharmaceutical, biotechnology, and healthcare industries worldwide. With a strong focus on quality, scientific excellence, and regulatory compliance, Eurofins provides end-to-end solutions across drug discovery, development, and safety assessment.

Roles & Responsibilities • Prepare Clinical Study Reports (CSR) for BA/BE studies and patient-based clinical trials (PK, PD, and clinical endpoint studies) based on clinical data received after study completion, in compliance with regulatory requirements, SOPs, client standards, and approved templates • Draft and finalize project reports with all required appendices in eCTD format, including: – Module 2: Clinical Summary – Module 5: Study reports, literature, appendices, and Bioanalytical Reports (BR) • Ensure reports meet applicable regulatory guidelines and submission requirements • Submit final compiled, signed clinical study reports (eCTD-compliant) to clients • Coordinate with Project Managers regarding report requirements, sponsor comments, and responses • Draft final reports and submit to sponsors through the Project Manager • Liaise with Bioanalytical (BR) and Statistics teams to integrate bioanalytical and statistical reports into the final submission • Address sponsor queries and incorporate feedback within agreed timelines • Ensure documentation quality, accuracy, and regulatory compliance throughout the reporting process Qualification • B.Pharm, M.Pharm Experience • Experience in clinical study report writing, BA/BE studies, or clinical research documentation preferred • Exposure to eCTD submissions and regulatory reporting is an advantage Skills • Strong understanding of BA/BE and patient-based clinical trials • Knowledge of PK, PD, and clinical endpoint studies • Familiarity with regulatory guidelines and SOP-driven environments • Experience with eCTD Modules 2 and 5 • Excellent medical/scientific writing skills • Strong coordination and communication skills • High attention to detail and compliance focus About the Organisation Veeda Clinical Research (Veeda CR) is a globally reputed Contract Research Organization providing end-to-end clinical research, bioanalytical, and regulatory services. Veeda is known for its regulatory compliance, scientific excellence, and high-quality clinical documentation supporting global submissions.

Roles & Responsibilities • Review and provide comments on draft clinical protocols, Informed Consent Documents (English ICD), Case Report Forms (CRF), and related documents as per SOPs and applicable regulatory guidelines • Review and comment on draft clinical reports, including clinic-related sections and appendices, in compliance with SOPs, regulatory guidelines, and sponsor requirements • Review final eCTD reports received from report writers to ensure regulatory and submission readiness • Ensure document reviews are completed within defined timelines and priority requirements • Review updated documents incorporating sponsor comments and regulatory observations to ensure compliance • Review sponsor comments and regulatory queries and provide appropriate responses within stipulated timelines • Participate in the review and maintenance of departmental SOPs • Coordinate with internal teams for implementation of new or revised SOPs • Ensure corrective and preventive actions (CAPA) are implemented for identified findings, comments, or gaps • Perform any additional responsibilities assigned by the reporting authority Qualification • B.Pharm (Any Specialization) • M.Pharm / MS / M.Sc (Science – Any Specialization) Experience • Experience in clinical research documentation, regulatory review, or clinical operations is preferred • Exposure to SOP-driven environments and regulatory guidelines is an advantage Skills • Strong knowledge of clinical research documentation and regulatory requirements • Attention to detail and compliance-focused mindset • Ability to manage timelines and work on priority-based tasks • Good written communication and document review skills • Ability to coordinate with cross-functional teams • Understanding of SOPs, eCTD structure, and sponsor/regulatory interactions About the Organisation Veeda Clinical Research (Veeda CR) is a globally recognized clinical research organization providing integrated solutions across clinical development, bioanalytical services, and regulatory support. Veeda is known for its strong compliance culture, scientific expertise, and commitment to delivering high-quality, regulatory-compliant clinical research services.

Roles & Responsibilities • Support Clinical Data Services with a focus on Medical Monitoring activities • Provide medical expertise for clinical trial oversight and safety evaluation • Support data collection, validation, storage, and analysis during clinical trials • Ensure clinical data accuracy, reliability, and regulatory compliance • Create, review, and validate protocol requirement specifications as per applicable SOPs • Assist in evaluating safety and efficacy data for ongoing clinical trials • Solve routine clinical data issues using standard guidelines and established procedures • Collaborate primarily with immediate team members and supervisors • Follow detailed to moderate instructions for daily tasks and new assignments • Ensure high-quality data outputs to support successful trial outcomes • Work as an individual contributor within a defined scope of responsibilities • Willingness to work in rotational shifts, as required Qualification • BE / Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm) Experience • 1–3 years of experience in: – Clinical Data Services – Clinical Data Management – Medical Monitoring or clinical trial support roles Skills • Strong analytical and problem-solving skills • Adaptable and flexible working style • Ability to work under defined guidelines and processes • Attention to detail and data accuracy • Ability to work effectively as part of a team About the Organisation Accenture is a global professional services company with leading capabilities in digital, cloud, security, and life sciences. With over 699,000 professionals across 120+ countries, Accenture supports the entire life sciences value chain-from research and clinical trials to regulatory, pharmacovigilance, and patient services-helping biopharma companies deliver safe, effective treatments and improve patient outcomes worldwide.

Roles & Responsibilities • Support Clinical Data Services activities within the Life Sciences R&D vertical • Perform Clinical eTMF (Electronic Trial Master File) management across the clinical trial lifecycle • Conduct discrepancy review, query generation, and query resolution in clinical databases • Support data validation, quality checks, and database accuracy reviews • Assist in creation and review of: – CRF Completion Guidelines (CCG) – SAE reconciliation guidelines • Identify, document, and escalate protocol deviations in clinical databases • Perform edit check validation by creating test cases and test scripts • Execute database validation (UAT) against specified CRF/eCRF requirements • Conduct TMF quality and completeness checks including: – Trial Master File Table of Contents – Initial and amended Full Protocol Packages (FPP) – End-of-trial checklists – Essential document reconciliation – Clinical Study Report (CSR) appendices • Perform eCTD-compliant document format checks for regulatory submissions including: – PDF property verification – Bookmarking and hyperlink validation – Compliance with Good Documentation Practices (GDP) • Collaborate with internal and client stakeholders to ensure regulatory readiness Qualification • Bachelor of Pharmacy (B.Pharm) Experience • 1–3 years of experience in: – Clinical Data Services – Clinical Data Management – Clinical eTMF management – Regulated clinical or regulatory documentation Skills • Strong attention to detail and documentation accuracy • Problem-solving and analytical skills • Ability to work under pressure in a regulated environment • Adaptable and flexible mindset • Strong client relationship and stakeholder management skills About the Organisation Accenture is a global professional services company with leading capabilities in digital, cloud, security, and life sciences operations. With over 699,000 professionals serving clients in more than 120 countries, Accenture supports pharmaceutical and biotech organizations across research, clinical trials, regulatory services, pharmacovigilance, and patient solutions—helping bring innovative therapies to market while improving patient outcomes worldwide.

Roles & Responsibilities • Support Clinical Data Management (CDM) activities including discrepancy review, query management, and data validation • Perform data quality checks to ensure accuracy, completeness, and regulatory compliance • Manage Clinical eTMF (Electronic Trial Master File) lifecycle activities • Conduct completeness and accuracy checks for: – Trial Master File (TMF) Table of Contents – Protocol packages and protocol amendments – End-of-trial and essential document checklists • Assist with CRF/eCRF review, edit check validation, and User Acceptance Testing (UAT) • Identify, document, and escalate protocol deviations as per SOPs • Support eCTD-compliant document preparation including: – PDF property checks – Bookmarking and hyperlink validation • Ensure adherence to Good Documentation Practices (GDP) • Collaborate with global cross-functional teams to support inspection and regulatory readiness Qualification • Bachelor of Pharmacy (B.Pharm) Experience • 0–3 years of experience in: – Clinical Data Services – Clinical Data Management – eTMF management – Regulated clinical documentation Skills • Strong attention to detail and documentation accuracy • Analytical and problem-solving skills • Ability to work under pressure in regulated environments • Adaptability and willingness to learn clinical systems and processes • Effective client communication and stakeholder coordination skills About the Organisation Accenture is a global professional services company with deep expertise in digital, cloud, security, and life sciences operations. With a workforce of over 790,000 professionals across 120+ countries, Accenture supports pharmaceutical and biotech companies throughout the product lifecycle—from clinical trials and clinical data management to pharmacovigilance and regulatory submissions—helping organizations deliver compliant, high-quality healthcare solutions worldwide.

Roles & Responsibilities • Ensure compliance with global pharmacovigilance regulations (EMA, EU GVP, ICH E2A/E2B, FDA, local guidelines) • Maintain and update pharmacovigilance documentation including SOPs and PV Master File (PSMF) • Assist during regulatory inspections, audits, and CAPA implementation • Support preparation, review, and submission of safety documents:  ICSRs, PSURs / PBRERs, DSURs, Risk Management Plans (RMPs) • Submit safety reports to EudraVigilance and other global safety databases • Perform literature screening and safety data evaluation • Assist in signal detection, risk minimization activities, and safety review meetings • Support preparation of SmPC, PIL, and package leaflets • Code and review adverse events using MedDRA and WHO-DD • Maintain accurate safety databases, trackers, and compliance logs • Complete mandatory PV trainings and stay updated with evolving regulations Qualification • B.PharmExperience • 0–1 year of experience in Pharmacovigilance • Freshers with PV training are eligible Skills • Basic understanding of pharmacovigilance regulations (EMA, EU GVP, ICH, FDA) • Knowledge of ICSR processing and safety reporting • Familiarity with MedDRA and WHO-DD coding • Strong attention to detail and documentation accuracy • Good written and verbal communication skills • Compliance-oriented and proactive learning mindset About the Organisation Lincoln Pharmaceuticals is a well-established Indian pharmaceutical company with a strong presence in domestic and international markets. The company is committed to quality, patient safety, and regulatory excellence, offering strong career growth opportunities in pharmacovigilance, regulatory affairs, and drug safety operations.

Roles & Responsibilities • Lead end-to-end clinical data management activities for global clinical trials • Collaborate with external vendors, internal teams, and trial stakeholders to align data management expectations • Gather, review, and finalize requirements for eCRFs and clinical data collection tools • Establish data quality standards, conventions, and ensure regulatory compliance • Set, track, and manage data management timelines and milestones • Ensure real-time inspection readiness and timely data deliverables • Review clinical data management documents, reports, and submission packages • Perform complex data reviews and manage queries in EDC systems • Work closely with Study Responsible Scientists (SRS), physicians, and clinical working groups • Contribute to process, system, and tool improvement initiatives Qualification • Bachelor’s degree (BS/BA) in Clinical Data Management, Health Sciences, Computer Sciences, or related field • Master’s degree or PhD preferred Experience • Around 2 years of experience in pharmaceutical, CRO, or biotech industry • Experience in clinical drug development and clinical data management Skills • Strong written and verbal communication skills (English) • Good understanding of clinical trial protocols and data management processes • Ability to work effectively with cross-functional and global teams • Knowledge of international clinical data management guidelines • Familiarity with data capture platforms, EDC systems, and data privacy regulations • Team leadership exposure preferred • Willingness to travel up to 10% (domestic/international) About the Organisation Johnson & Johnson is a global healthcare leader committed to transforming lives through innovative medicines, medical devices, and data-driven healthcare solutions. With a strong focus on clinical research and patient outcomes, the company plays a critical role in advancing global health through science, technology, and collaboration.