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Role & Responsibilities • Act as a trusted advisor to leaders on people, culture, and organizational topics • Drive people initiatives and change management (local and global) • Support organizational transformations, employee relations, and engagement • Use data and insights to influence decisions and outcomes • Build strong partnerships across HR and business teams • Develop and execute medical interaction plans with key accounts • Address employee requests, providing solutions and executing strategic initiatives • Design and implement change management strategies for local and global initiatives • Manage and resolve employee relations issues, focusing on collaboration and retention • Foster a collaborative environment between leadership and employees • Stay updated on internal trends and external market dynamics to deliver impactful solutions Qualifications • University degree in Human Resources or related field (MBA preferred) • Fluency in English and local language (spoken and written) Experience • Proven experience as an HR Business Partner or People Partner • Strong stakeholder management and influencing skills • Experience in Talent Management, Organizational Design, and Change Management • Ability to work independently and collaborate with diverse teams • Familiarity with local labor laws and conflict resolution • Experience in HR data analytics and driving data-driven decisions Skills • Good understanding of HR practices, employee relations, and organizational dynamics • Strong consulting and influencing skills • Business acumen and understanding of the HR-business alignment • Agile mindset with the ability to manage and drive change projects • Strong communication, empathy, and problem-solving skills • Ability to manage multiple priorities effectively About The Company • Bayer is a global purpose-driven organization focused on improving lives through innovative solutions in various fields. The company fosters a collaborative and agile working culture, offering employees autonomy, high visibility, and the chance to make a real impact on the business.
Roles & Responsibilities: • Manage end-to-end TMF and document management operations in compliance with ICON SOPs, client requirements, and regulatory guidelines • Lead and mentor 20–30 TMF professionals, ensuring high performance and quality delivery • Coordinate TMF activities across multiple studies and clients • Generate and present TMF status reports for internal stakeholders and clients • Drive process improvement initiatives to enhance efficiency and quality • Ensure TMF inspection readiness and participate in internal and external audits • Oversee TMF archiving activities and study close-out documentation • Liaise with clinical study teams, training departments, and clients • Manage quality control, tracking, and compliance metrics • Support departmental and cross-functional projects as assigned Qualification: • Bachelor’s degree in Science, Medicine, Pharmacy, Life Sciences, or equivalent • Strong understanding of clinical study start-up, maintenance, and close-out activities Experience: • 12+ years of experience in TMF Operations within clinical research or CRO environments • 3+ years of people management experience managing large teams (20–30 members) Skills: • Excellent organizational, communication, and stakeholder management skills • Proven ability to manage multiple projects and global clients • Strong analytical, problem-solving, and conflict management skills • Willingness to travel up to 25% (domestic/international) About the Organisation: ICON plc is a global leader in healthcare intelligence and clinical research, known for its strong culture of Accountability, Collaboration, Partnership, and Integrity. ICON provides professionals the opportunity to work on global clinical trials, shaping the future of drug development while delivering high-quality solutions to clients worldwide.
Role & Responsibilities • Perform medical review of clinical trial and post-marketing safety cases (AEs, SAEs, ADRs) • Review and ensure accuracy of narratives, coding, seriousness, expectedness, and causality • Compose and medically review Analyses of Similar Events (AOSE) • Provide medical oversight and coding review for AEs, SAEs, concomitant medications, and medical history • Act as internal medical consultant to pharmacovigilance case processing teams • Review protocols, Investigator Brochures, CRFs, and safety sections for appropriate data capture • Conduct aggregate safety reviews (DSUR, RMP, PBRER, ad-hoc regulatory reports) • Maintain and oversee product safety profiles across lifecycle stages • Ensure compliance, quality, and timely service delivery as per regulatory and contractual timelines • Provide guidance and mentorship to safety team members on medical assessments • Maintain and update safety watch lists, labeling, RSIs, and expectedness documents • Lead and support training initiatives, audits, inspections, and product transitions • Review and approve Project Safety Plans and Medical Monitoring Plans • Represent medical safety findings in internal and client meetings • Act as Lead Safety Physician or provide backup medical support on assigned projects • Support medical escalations and EU QPPV-related activities when required • Provide 24-hour medical safety support on assigned projects (as applicable) • Participate in signal detection activities and safety strategy discussions • Stay updated with global pharmacovigilance regulations and industry developmentsQualification • Medical degree (MBBS or equivalent) from an internationally recognized institution • Valid medical license (preferred)Experience • Minimum 3 years of clinical practice post medical qualification • Minimum 2 years of experience in pharmacovigilance / pharmaceutical industry (preferred) • Experience in ICSR review and aggregate safety reportingSkills• Strong knowledge of clinical medicine and drug safety • In-depth understanding of GCP, ICH, and global PV regulations • Hands-on experience with safety databases and PV systems • Strong analytical, medical writing, and decision-making skills • Excellent verbal and written communication skills • Ability to work independently and within matrix teams • Proficiency in MS Word, Excel, and PowerPoint About the Company• IQVIA is a global leader in clinical research, pharmacovigilance, and healthcare analytics
Roles & Responsibilities: • Prepare and review clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and other clinical trial documents in line with regulatory guidelines and industry standards • Collaborate with cross-functional teams, including clinical operations, regulatory affairs, and biostatistics, to ensure accuracy and completeness of deliverables • Interpret and summarize clinical trial data from study reports, statistical analyses, and scientific literature • Assist in preparation of regulatory submissions (INDs, NDAs, BLAs, MAAs) with high-quality medical writing support • Participate in project meetings, provide updates on medical writing activities, and contribute to project planning and timelines • Stay current with developments in medical writing, regulatory requirements, and therapeutic areas relevant to projects • Mentor junior medical writers and provide guidance on best practices for document preparation Qualifications: • Bachelor’s degree in Life Sciences, Pharmacy, or related field; advanced degree (MD, PhD, PharmD) preferred Experience: • Minimum 5 years of experience in medical writing within pharmaceutical, biotechnology, or CRO industry • Proficiency in interpreting clinical trial data, including statistical analyses and safety reports • Strong understanding of regulatory guidelines (ICH, FDA, EMA) for clinical trial documents and submissions Skills: • Excellent written and verbal communication skills • Detail-oriented with strong organizational and time management abilities • Ability to work independently and collaboratively in multidisciplinary teams • Proficiency in Microsoft Office Suite and familiarity with document management systems (e.g., SharePoint) About the Organization: MS Clinical Research Pvt Ltd is a dynamic and innovative clinical research organization specializing in clinical trials and comprehensive medical writing services. The company is committed to advancing medical research, supporting regulatory submissions, and improving patient outcomes through high-quality, scientifically accurate documentation and collaborative project execution.
Roles & Responsibilities: • Lead the planning and execution of clinical studies across Skin, Hair, and Oral domains • Ensure studies are conducted in alignment with organizational goals, timelines, and budgets • Oversee day-to-day operations of the Clinical Operations team • Develop study plans, timelines, and resource allocation strategies • Ensure all study activities are executed as per protocol schedules and client expectations • Review study documents including protocols, CRFs, questionnaires, and monitoring plans • Identify operational risks and implement mitigation strategies • Conduct Site Initiation Visits (SIVs), monitoring visits, and close-out activities • Ensure proper delegation of study responsibilities and oversight at all sites • Maintain strong relationships with investigators and site personnel • Oversee completion of protocol, SOP, and GCP training for internal teams and site staff • Monitor adherence to regulatory requirements and internal quality standards • Act as primary point of contact for study-related communication with sponsors • Coordinate multisite studies, ensuring consistency in execution, data quality, and reporting • Ensure timely completion of study documentation and support audit readiness • Drive continuous improvement in clinical operational processes Qualifications: • Master’s/Bachelor’s degree in Life Sciences, Pharmacy, Cosmetic Technology, or related field Experience: • 5–10+ years in clinical trials with at least 2–3 years in a supervisory/managerial role • Experience in cosmetic/dermatology clinical studies highly desirable Skills: • Strong knowledge of clinical research processes, GCP, and regulatory guidelines • Expertise in managing Skin, Hair, Cosmetic, or Dermatology-based clinical studies (preferred) • Excellent communication and stakeholder management skills • Ability to lead teams and manage multiple projects simultaneously • Strong analytical thinking, documentation, and problem-solving skills About the Organization: The organization specializes in conducting high-quality clinical trials in cosmetic, dermatology, and life sciences domains. It focuses on regulatory compliance, operational excellence, and delivering innovative clinical solutions while fostering a collaborative and professional work environment.
Roles & Responsibilities: • Conduct site initiation, routine monitoring, and close-out visits to ensure compliance with study protocols, GCP, and regulatory requirements • Build and maintain strong relationships with investigative sites, investigators, and study coordinators • Perform routine monitoring visits to assess site performance, data integrity, and regulatory compliance • Ensure timely resolution of data queries and issues identified during monitoring visits • Ensure all study activities are conducted according to approved protocols, SOPs, and regulatory guidelines • Collaborate with investigators to address and resolve protocol-related queries • Assist in preparation and submission of regulatory documents to ethics committees and regulatory authorities • Collaborate with data management teams for accurate and timely data collection and entry • Perform source data verification and data validation activities • Monitor and report adverse events as per regulatory and safety reporting procedures • Provide training and support to site staff on study protocols, data collection, and regulatory compliance • Act as a resource for investigators and site staff throughout the study Qualifications: • Bachelor’s degree in Life Sciences or a related field Experience: • Minimum 3 years as a Clinical Research Associate with proven site management and monitoring experience • Familiarity with regulatory requirements and guidelines governing clinical trials Skills: • Excellent verbal and written communication skills • Strong organizational and time management skills with attention to detail • Ability to work effectively in cross-functional teams and independently • Willingness to travel to investigative sites as required About the Organization: MS Clinical Research Pvt Ltd is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. The company focuses on conducting high-quality clinical trials, ensuring regulatory compliance, and supporting the development of innovative medical solutions in a collaborative and dynamic environment.
Roles & Responsibilities: • Develop, program, and validate ADaM datasets as per CDISC standards. • Create Tables, Listings, and Figures (TLFs) using SAS and/or R. • Implement Statistical Analysis Plans (SAP) and Statistical Programming Plans (SPP). • Ensure compliance with regulatory and industry standards (CDISC – SDTM, ADaM). • Collaborate closely with biostatisticians and clinical teams to ensure data accuracy. • Develop reusable macros and automate programming processes for efficiency. • Perform independent QC checks on statistical outputs and deliverables. • Support programming activities across multiple therapeutic areas including Oncology, Neuroscience, and Immunology. Qualifications • Graduate / Postgraduate in Life Sciences, Engineering, Statistics, or related disciplines.Experience: • 3 to 12 years of experience in clinical or biostatistical programming. • Hands-on experience in ADaM, TLF development, and clinical trial data analysis. Skills: • Strong expertise in SAS and/or R programming. • In-depth knowledge of CDISC standards (SDTM, ADaM). • Experience working with clinical trial protocols and regulatory guidelines. • Proficiency in TLF generation and data manipulation techniques. • Strong analytical, problem-solving, and attention-to-detail skills. • Exposure to additional tools such as Python or SQL (preferred). • Basic understanding of machine learning concepts applied to clinical data (preferred). About the Organisation: The organization is a leading clinical research and data analytics-driven company supporting global clinical trials across multiple therapeutic areas, offering a collaborative work environment, exposure to regulatory-compliant projects, and long-term career growth opportunities in statistical and clinical programming.
Role & Responsibilities • Build and maintain peer-level scientific relationships with Neuroscience KOLs • Drive high-quality scientific discussions across Parkinson’s disease, Multiple Sclerosis, migraine, and related indications • Support upcoming product launches, CMEs, and advisory board meetings • Conduct compliant scientific exchange with neurologists and HCPs • Generate actionable medical insights from field interactions • Collaborate cross-functionally with Medical Affairs, Marketing, and Commercial teams • Contribute to medical strategy execution and launch readiness Qualification • MBBS / BDS / PharmD / MSc / PhD Experience • 1–2 years’ experience in Medical Affairs or MSL roles • Neuroscience therapeutic experience preferred Skills • Strong scientific communication and presentation skills • Ability to engage neurologists and senior clinicians in scientific dialogue • Good understanding of clinical data and treatment paradigms • Self-driven and capable of working independently in the field • Willingness to travel within assigned territories Why Join • Opportunity to work with an innovation-driven neuroscience portfolio • Early exposure to launch excellence and strategic medical affairs activities • Direct impact on patient care through scientific engagement • Strong platform for long-term growth in Medical Affairs and leadership roles
Roles & Responsibilities: • Manage and develop existing and new key accounts and government business at zonal level for IVD instruments and reagents • Drive sales growth, forecasting monthly and annual targets with profitability accountability • Handle key account management, customer relationship management, satisfaction, and retention • Analyze key account performance and market share, prepare corrective action plans • Align with zonal teams and cascade business strategies for growth • Generate leads, negotiate, and successfully close deals • Coordinate with customers and internal teams for timely delivery and payment collection • Conduct periodic reviews with government and key institutional customers • Execute innovative promotional activities, roadshows, CMEs, and product demonstrations • Monitor market trends, competition, and submit regular reports, DCRs, and MIS on TAB • Ensure compliance with company systems, processes, and ethical sales practices Qualification: • BE / B.Tech / B.Sc / M.Sc / B.Pharm / Diploma Experience Required: • 2–5 years of Key Account and Government Business experience in the IVD industry Skills: • Key account & govt. business handling • Strategic sales planning & forecasting • Negotiation & relationship management • Market analysis & reporting • Strong communication and leadership skills About the Organization: Erba Transasia is a leading in-vitro diagnostics company offering comprehensive diagnostic solutions across clinical chemistry, immunoassays, hematology, and molecular diagnostics, with a strong presence in India and global markets.
Roles & Responsibilities: • Promote assigned IVD (in-vitro diagnostics) products to customers at defined frequencies. • Generate leads and convert opportunities into sales. • Coordinate with customers, credit control, and internal teams for timely and outstanding payment collections. • Build and maintain strong relationships with customers and distributors. • Ensure compliance with company systems, policies, and sales processes. • Negotiate effectively and close sales deals successfully. • Ensure timely and accurate delivery of products to customers. • Monitor market trends, competitor activities, and product performance and report insights to management. • Prepare daily call reports, update attendance, capture product complaints, and record opportunities using the TAB system. • Submit Field Expense Statements (FES) within stipulated timelines. • Support roadshows, CMEs, and product demonstrations. • Continuously update technical knowledge and selling skills. Qualification: • B.Sc / B.Pharm / B.Tech / B.E / Diploma. Experience: • Minimum 2 years of experience in IVD Government Sales. Skills: • Strong sales, negotiation, and relationship-building skills. • Good understanding of IVD products and government sales processes. • Ability to coordinate with multiple stakeholders and internal teams. • Strong communication, reporting, and documentation skills. • Willingness to travel extensively within the assigned territory. About the Organization: Erba Transasia is a leading diagnostics company with a strong presence in India and global markets, offering a comprehensive range of in-vitro diagnostic solutions across clinical chemistry, immunoassays, hematology, and molecular diagnostics. Known for innovation, quality, and customer-centric solutions, Erba Transasia supports healthcare providers with reliable diagnostic technologies.
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.
Role & Responsibilities • Assist doctors and nurses in patient care • Monitor vital signs • Maintain patient hygiene and comfort • Prepare patients for procedures • Maintain ward cleanliness Qualification • GNM / B.Sc NursingVacancies no - 24 Experience • Clinical/hospital experience preferred Skills • Patient care • Ward management • Communication skills About Organization DHFWS Bangalore works to strengthen nursing and patient care services in district hospitals.Application Closing date28-01-2026Official NotificationClick Here
Role & Responsibilities • Provide general OPD consultation • Diagnose and treat common illnesses • Manage minor emergencies • Prescribe medications and maintain records • Refer serious cases to higher centers • Participate in public health programs Qualification • MBBSVacanices no - 02 Experience • Experience in clinical practice preferred Skills • Patient examination • Disease diagnosis • Communication with patients About Organization DHFWS Bangalore delivers primary and secondary healthcare services across the district.Application Closing date28-01-2026Official NotificationClick Here
Role & Responsibilities • Perform general surgical procedures and emergency surgeries • Examine, diagnose, and manage surgical patients • Conduct pre-operative and post-operative care • Attend emergency and trauma cases • Maintain patient case sheets and surgical records • Guide junior doctors and nursing staff • Follow hospital safety, sterilization, and infection control protocols Qualification • MD/MS in General Surgery Experience • Experience in government/private hospital preferred • Fresh specialists may apply as per norms Skills • Surgical and operative skills • Clinical decision-making • Emergency management • Team coordination About Organization District Health & Family Welfare Society (DHFWS) Bangalore works under the Karnataka Health Department, providing public healthcare services and strengthening district-level medical infrastructure.Closing date28-01-2026Official NotificationClick Here
Roles & Responsibilities • Review and approval of MBR, APQR, and QA documentation • Handle deviations, change control, CAPA, complaints, and QMS activities • Execute and review media fill studies, process simulations, and equipment qualification • Ensure cGMP and regulatory compliance (USFDA, EU, CDSCO) • Coordinate with cross-functional teams for compliance and audit readiness • Use QA systems such as Trackwise, SAP, LIMS, DMS, and Minitab Available Positions • QA – Documentation (Team Leader / Manager) Qualification: B.Pharm / M.Pharm Experience: 10–13 years • QA – QMS (Executive / Sr. Executive) Qualification: B.Pharm / M.Pharm Experience: 3–7 years • QA – Media Fill / Validation (Asst. Manager) Qualification: B.Pharm / M.Pharm Experience: 8–10 years • QA – Media Fill / Validation (Executive / Sr. Executive) Qualification: B.Pharm / M.Pharm Experience: 3–7 yearsSkills • Sterile QA operations • QMS (Deviation, CAPA, Change Control) • Media fill & validation activities • Regulatory compliance • Documentation & audit handling About the Organization Micro Labs Limited is a reputed Indian pharmaceutical company with strong expertise in sterile manufacturing and global regulatory compliance, offering stable growth and exposure to advanced quality systems.
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 • 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.
Roles & Responsibilities • Perform routine analytical testing of in-process and isolated samples • Analyze early intermediates and APIs using chromatographic and wet analytical techniques • Execute method qualification and support instrument calibration activities • Maintain accurate and compliant documentation using Electronic Lab Notebooks (ELN) • Ensure adherence to GxP guidelines and quality standards • Handle general laboratory responsibilities and support ongoing Analytical R&D activities • Contribute to API development and chemical research programs Qualification • M.Pharm (Pharmaceutical Analysis / Analytical Chemistry preferred) Experience • Relevant experience in Analytical R&D within pharmaceutical or CRO/CRDMO environments preferred Skills • Strong theoretical and practical knowledge of analytical chemistry • Hands-on experience with chromatographic techniques • Understanding of method qualification and instrument calibration • Knowledge of GxP documentation and compliance standards • Proficiency in MS Office tools (Word, Excel, PowerPoint) • Strong communication, documentation, and teamwork skills • High attention to detail with a proactive and ethical work approach • Willingness to work in shifts, if required About the Organisation Syngene International Ltd. is a leading global Contract Research, Development, and Manufacturing Organization (CRDMO) supporting pharmaceutical and biotechnology companies worldwide. Known for its strong scientific capabilities and innovation-driven culture, Syngene offers professionals exposure to cutting-edge API development, analytical research, and global drug discovery programs.
Roles & Responsibilities • Manage end-to-end Clinical Data Management deliverables for assigned clinical studies • Review and evaluate clinical data generated from imaging components of sponsor trials • Participate in client and project meetings as required • Understand study requirements for data collection and implementation • Collaborate with project teams to develop study-specific edit check criteria • Define, execute, and review edit checks; resolve discrepant data • Perform study setup including database structure, specifications, and TF design • Coordinate receipt and processing of electronic and ancillary data from external sources • Review clinical data for errors and inconsistencies and drive resolution • Track outstanding data issues and ensure timely closure • Maintain complete, accurate, and audit-ready study documentation • Ensure all CDM activities comply with SOPs, regulatory guidelines, and quality standards • Support SOP updates and contribute to continuous process improvement • Maintain technical and industry knowledge through ongoing training Qualification • Bachelor’s degree in Computer Science, Life Sciences, or a related field • Equivalent professional experience may be considered Experience • Minimum 1 year of experience in Clinical Data Management • Experience in pharma, biotech, or CRO environment preferred Skills • Strong knowledge of Clinical Data Management processes • Understanding of relational database structures and data validation • Familiarity with SAS is desirable • Proficiency in MS Word, Excel, and Access • Knowledge of clinical trial terminology • Excellent attention to detail and problem-solving abilities • Strong communication, documentation, and organizational skills • Ability to work independently and collaboratively in a dynamic environment About the Organisation Clario is a global leader in clinical trial endpoint technology, dedicated to transforming evidence generation and improving patient outcomes. The company supports life-changing therapies through innovation, data excellence, and a purpose-driven culture, offering flexible work options, competitive benefits, and opportunities to make a meaningful impact in global clinical research.