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Roles & Responsibilities• Handle batch manufacturing and filling activities in sterile area (Injectables, BFS, Eye drops)• Operate ampoule/vial washing (Macofar), Rota filling, BFS machines and Autoclave• Conduct media fill studies and equipment qualification• Lead qualification studies in sterile manufacturing (QA senior roles)• Perform QC testing for finished products and stability samples• Conduct analytical method validation and method transfer• Handle QMS documentation and compliance activities• Perform microbiological testing including sterility testing, MLT, environmental monitoring• Ensure adherence to regulatory and GMP guidelinesQualification• B.Pharm / M.PharmExperience• Freshers (QC – male candidates only)• 0–12 years depending on role• Production: 2–8 years• QA: 3–10 years• QC: 0–6 years• Microbiology: 6–12 yearsSkills• Sterile manufacturing exposure• Media fill & validation knowledge• Equipment qualification handling• Analytical testing & stability studies• QMS & regulatory documentation• Environmental monitoring• GMP & compliance awarenessAbout The CompanyMicro Labs Limited is a leading Indian pharmaceutical company specializing in sterile formulations including injectables and ophthalmic products. The organization operates in regulated markets and provides strong exposure to quality systems, GMP compliance, and large-scale pharmaceutical manufacturing.
Roles & Responsibilities• Enter clinical trial data accurately using Clinical Data Management (CDM) systems• Review, track, and assist in resolving data queries in coordination with sponsors and monitoring teams• Maintain records of CRF receipt, data entry status, and query resolution• Support database testing, edit checks, and data reconciliation activities• Assist in medical coding, electronic data transfers, and generation of reports and listings• Coordinate with lead CDMs and project teams to ensure smooth study execution• Generate project updates, reports, and documentation as required• Participate in project meetings and assist in preparing agendas and meeting minutes• Support study tracking tools and data management systems (CRF flow, query flow, safety reports, Novotrak)• Contribute to process improvement initiatives and provide general administrative support• Ensure compliance with SOPs, GCDMP guidelines, ICH-GCP, and company quality standardsQualification• Graduate in Clinical Sciences, Life Sciences, Pharmacy, or allied disciplinesExperience• Freshers can apply• 6 months to 1 year of experience in clinical data management or clinical research is preferredSkills• Basic knowledge of clinical data management and CDM software• Strong attention to detail and data accuracy• Good communication and teamwork skills• Ability to follow SOPs and regulatory guidelinesAbout the OrganizationNovotech is a leading global CRO providing full-service clinical development solutions, supporting innovative clinical trials across multiple therapeutic areas while fostering an inclusive and growth-oriented work culture.
Roles & Responsibilities:• Support global safety literature screening for ICSR identification and signal detection• Perform pharmacovigilance literature surveillance as per regulatory requirements• Screen and review literature (articles, abstracts, citations) for safety information• Triage literature for GSK marketed and development products using defined criteria• Support periodic reporting and signal detection activities• Maintain up-to-date product knowledge and master drug lists• Perform quality checks on triaged literature and ensure documentation accuracy• Collaborate with PV, Medical Affairs, and Regulatory teamsQualification:• Bachelor’s degree in Life Sciences / Pharmacy / Pharmacology / Medical disciplineExperience:• 1–5 years of experience in literature review, pharmacovigilance support, or medical writing• Pharmaceutical industry experience preferred (Drug Safety / Regulatory / Clinical / Medical Affairs)Skills:• Working knowledge of pharmacovigilance regulations and methodologies• Strong scientific literature searching and screening skills• Good understanding of medical and scientific terminology• Excellent attention to detail and analytical skills• Strong communication, interpersonal, and teamwork skills• Good computer skills and experience with web-based applicationsAbout the Organization:GSK is a global biopharmaceutical company focused on vaccines and specialty medicines, uniting science, technology, and talent to get ahead of disease together while prioritizing patient safety and public health.
Roles & Responsibilities:• Assist in processing Individual Case Safety Reports (ICSRs)• Perform adverse event (AE) and serious adverse event (SAE) case intake• Support case triage, data entry, and quality checks• Ensure compliance with global pharmacovigilance regulations• Work with medical terminologies such as MedDRA and WHO-DD• Maintain accurate drug safety documentation• Collaborate with senior drug safety associates and PV teamsQualification:• M.Pharm / B.Pharm / PharmD / MSc Life SciencesExperience:• Freshers onlyNo. of Openings: 30Skills:• Basic understanding of Pharmacovigilance and drug safety processes• Awareness of adverse events and clinical pharmacology• Familiarity with medical terminology• Good attention to detail and willingness to learnAbout the Organization:The company is a global pharmaceutical organization with established pharmacovigilance operations, offering freshers hands-on exposure and a strong foundation in drug safety and clinical safety operations.Interested and eligible candidates should share their updated CV to email: sahana.s@randstad.in
Roles & Responsibilities• Act as lead data manager for one or more clinical studies and support senior leads as required• Apply study protocols to daily data management activities and guide team members accordingly• Serve as liaison with Project Lead, clients, and management for all data management activities• Develop, maintain, and review data management documentation in line with CDM guidelines• Deliver study-specific training to data management project staff• Produce regular project status reports and monitor study metrics• Support bid activities including proposal inputs and bid defense participation when required• Forecast project hours, identify resource needs, and flag out-of-scope activities for contract modification support• Mentor junior team members and provide technical guidance across study tasks• Assist with administrative and financial management of assigned projects• Execute end-to-end data management activities independently with strong quality focusQualification• Bachelor’s degree or equivalent relevant academic or vocational qualificationExperience• Minimum 4+ years of experience in a Clinical Data Manager role• Mandatory hands-on experience with Veeva EDC• End-to-end data management experience including study set-up, conduct, and close-out• Oncology trial experience preferredSkills• Strong knowledge of clinical data management processes and regulatory requirements• Proficiency with interactive computer programs and EDC systems• Excellent written and verbal communication skills with strong English proficiency• Strong organisational, analytical, and problem-solving abilities• High attention to detail and confidentiality handling of clinical data• Ability to work independently with minimal supervision• Strong customer focus and interpersonal skills• Flexibility and adaptability in dynamic project environments• Ability to train, mentor, and direct study teams• Strong timeline management and prioritisation skillsAbout the CompanyThermo Fisher Scientific is a global leader in serving science, supporting pharmaceutical and biotechnology companies through its PPD® clinical research services portfolio. With operations across more than 100 countries, the organization delivers end-to-end clinical development and data management solutions, enabling high-quality, compliant, and efficient clinical trials that bring life-changing therapies to patients worldwide.
Roles & Responsibilities• Manage and lead FSP Clinical Data Management teams, including hiring, performance management, coaching, mentoring, and professional development• Oversee workload distribution, resourcing, and global allocation planning for assigned staff• Ensure timely, high-quality, and budget-compliant delivery of data management activities across portfolios• Provide oversight, guidance, and coaching to portfolio teams to meet client and project expectations• Ensure staff adherence to SOPs, regulatory guidelines, and client-specific processes• Support operational execution of studies and portfolios with strong focus on quality and efficiency• Act as escalation point for data management issues and support study managers as required• Participate in development and implementation of CDM processes, procedures, and training programs• Review and approve timesheets, expenses, leave requests, and overtime• Maintain confidentiality and integrity of clinical and proprietary client data• Collaborate with senior leadership on strategic resourcing, reporting, and performance planningQualification• Bachelor’s degree or equivalent relevant academic or vocational qualificationExperience• 12+ years of experience in Clinical Data Management or related clinical research roles• Minimum 5+ years of leadership and people management experience• Strong hands-on experience operating within the FSP business modelSkills• Strong knowledge of clinical data management processes and regulatory requirements• Ability to act as subject matter expert for data management activities• Excellent analytical, problem-solving, and decision-making skills• Strong written and verbal communication skills with good command of English• High attention to detail and numerical accuracy• Ability to manage, motivate, and develop high-performing teams• Strong project planning, prioritisation, and timeline management skills• Ability to work effectively in global, cross-functional, and matrix environmentsAbout the CompanyThermo Fisher Scientific is a global leader in serving science, supporting pharmaceutical and biotechnology companies through its PPD® clinical research services portfolio. With operations spanning more than 100 countries, the organization delivers end-to-end clinical development, data management, and regulatory solutions, enabling faster delivery of life-changing medicines while maintaining the highest standards of quality, compliance, and scientific excellence.
Roles & Responsibilities• Act as account lead or primary internal/external contact for standalone coding studies or accounts• Manage customer relationships, including coding-related negotiations on timelines, budgets, and scope• Provide leadership and senior support to Lead Coders on large, global clinical studies• Serve independently as Lead Data Coder and/or Coding Reviewer for multiple projects• Perform the role of Data Operations Coordinator (DOC), Data Team Lead (DTL), or customer site lead as required• Manage and oversee quality control procedures across studies• Perform and oversee Serious Adverse Event (SAE) reconciliation activities• Collaborate with customers to develop solutions and action plans for issues, risks, and escalations• Proactively identify quality risks and ensure on-time project delivery• Identify and manage out-of-scope activities and conduct due diligence• Manage project team resource planning and capacity• Mentor and train team members to build coding and CDM expertise• Drive process improvements, best practices, and quality initiatives within CDM and coding functions• Support development and implementation of new technologies• Participate in or present at local and international scientific forums• Contribute expert input to development and maintenance of SOPs and work instructions• Ensure effective communication and collaboration with CDM teams and client stakeholdersQualification• Qualification in Pharmacy, Dental, Medical, Nursing, Life Sciences, or related field• High School Diploma with relevant experience may be considered as per role requirementsExperience• Minimum 7 years of relevant experience in clinical trials within data management and/or coding• Proven experience managing multiple global studies, complex customer negotiations, and bid defense meetingsSkills• Expert knowledge of medical dictionaries (MedDRA, WHODD, ICD-9, etc.)• Strong understanding of medical terminology, pharmacology, anatomy, and physiology• Advanced knowledge of clinical data management processes and systems• Excellent understanding of clinical drug development processes• Strong leadership, team management, and mentoring skills• Excellent project management, organizational, and communication skills• Sound financial management and budgeting knowledge• Ability to make independent decisions and manage cross-functional teams effectivelyAbout the OrganizationIQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights, helping life sciences companies accelerate the development and commercialization of innovative medical treatments to improve patient and population health worldwide.
Roles & Responsibilities• Serve independently as Clinical Data Coder, Lead Coder, or Data Operations Coordinator (DOC) for one or more protocols• Manage delivery of coding activities and standalone coding projects across the study lifecycle• Validate and test coding applications, reports, datasets, edits, and coding-related programming activities• Perform comprehensive data review, write and resolve data clarifications• Manage coding-related timelines with guidance from DOC, Data Team Lead (DTL), or Manager• Perform Serious Adverse Event (SAE) reconciliation activities• Act as backup for Lead Coder, DOC, or DTL when required• Execute quality control procedures and support implementation of new technologies• Provide independent coding and project-related solutions to the Data Management team• Handle audit and inspection requirements for assigned studies• Ensure compliance with SOPs, work instructions, and regulatory requirements• Maintain effective communication and working relationships with internal teams and stakeholdersQualification• Degree in Pharmacy, Dental, Medical, Nursing, Life Sciences, or related field• LPN (Licensed Practical Nurse) – State Licensure (where applicable)Experience• Minimum 2 years of relevant experience in clinical data management and/or medical coding• Equivalent combination of education, training, and experience may be consideredSkills• Strong knowledge of medical terminology, pharmacology, anatomy, and physiology• In-depth experience with medical dictionaries (MedDRA, WHODD, etc.)• Understanding of end-to-end clinical data management processes• Excellent attention to detail and problem-solving ability• Good understanding of database technologies related to data management and coding• Strong written and verbal communication skills in English• Ability to work independently and collaborate effectively with cross-functional teamsAbout the OrganisationIQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights, enabling life sciences organizations to accelerate the development and commercialization of innovative treatments that improve patient outcomes worldwide.
Roles & Responsibilities• Lead and manage FSP Clinical Data Management staff including hiring, onboarding, performance management, coaching, and career development• Oversee workload allocation, global resourcing, and utilization for assigned team members• Provide oversight, guidance, and coaching to ensure tasks are delivered accurately, on time, and within budget• Partner with senior leadership on training, mentoring, and capability development of project staff• Ensure compliance with SOPs, regulatory guidelines, and client expectations• Support operational execution of studies and portfolios with a strong focus on quality delivery• Act as a subject matter expert for Clinical Data Management processes• Participate in development and implementation of CDM processes, procedures, and training programs• Review and approve time records, expense reports, leave requests, and overtime• Collaborate closely with client’s global data science teams in a mature FSP delivery model• Support continuous improvement initiatives, risk management, and issue resolution across studiesQualification• Bachelor’s degree or equivalent with relevant academic or vocational qualificationExperience• 12+ years of overall experience relevant to Clinical Data Management• Minimum 5+ years of people leadership or managerial experience• Strong hands-on experience working within an FSP business model• Experience supporting global clinical trials across multiple phases preferredSkills• Strong understanding of CDM processes, EDC systems, and data quality management• Ability to operate in compliance with regulatory requirements, SOPs, and client standards• Strong analytical, problem-solving, and numerical skills• Excellent written and verbal communication skills in English• Ability to manage confidential clinical and proprietary client data• Strong interpersonal, stakeholder management, and team leadership skills• Ability to plan, prioritize, and adapt timelines based on project demands• Capability to manage, motivate, and supervise global teams effectivelyAbout the CompanyThermo Fisher Scientific is a global leader in serving science, enabling customers to make the world healthier, cleaner, and safer. With operations spanning clinical research, laboratory services, diagnostics, and biopharma solutions, the organization supports pharmaceutical, biotechnology, and research partners worldwide.
Roles & Responsibilities• Assist in assembly, publishing, tracking, and archiving of global regulatory submissions• Author, compile, and manage electronic regulatory submissions (eCTD and other formats)• Support regulatory pathway research for new, modified, and existing products• Provide regulatory strategy input to product development and cross-functional teams• Review labeling, Instructions for Use (IFU), and package inserts for global compliance• Evaluate promotional and advertising materials for regulatory adherence• Assess product and process changes for regulatory impact• Communicate with regulatory authorities under supervision• Apply FDA, EU MDR, and other global regulatory requirements to business practicesQualification• Bachelor’s degree in Life Sciences, Pharmacy, Engineering, or related disciplineExperience• Minimum 3+ years of experience in Regulatory Affairs, Quality, or Engineering• At least 1+ year experience in medical devices or orthopaedics preferredSkills• Strong knowledge of FDA, EU MDR, and global medical device regulations• Experience with regulatory submissions and electronic publishing• Labeling and promotional material review expertise• Regulatory risk assessment and strategy development• Excellent writing, documentation, and communication skills• Strong attention to detail and ability to multitask• Proficiency in MS Office and regulatory documentation tools• Regulatory Affairs Certification (RAC – US/EU)About the OrganizationZimmer Biomet is a global leader in medical technology with nearly 100 years of innovation, specializing in orthopaedic solutions and advanced medical devices, offering strong global exposure and long-term career growth in regulatory affairs.
Roles & Responsibilities• Maintain patient safety as the highest operational priority• Escalate patient safety issues promptly for appropriate resolution• Communicate with investigator sites via email and approved communication channels• Provide administrative and operational support to Global Investigator Support (GIS) teams and Coordinators• Prepare airway bills and shipping documentation for study-related materials• Follow up on delivery errors and specimen pending arrival reports• Support Investigator Portal and Sponsor Portal access and login issues• Compile and communicate updates related to new policies and procedures• Search, update, and maintain investigator site databases accurately• Escalate site-related information to assigned global coordinators• Resolve simple to moderate system-generated hold issues• Investigate, respond to, and document project-related queries• Record service failures and escalate unresolved issues appropriately• Manage training folders and maintain updated documentation• Review SOPs and departmental documents for compliance• Track, monitor, and report workflow metrics• Complete onboarding, mandatory corporate, and departmental trainingQualification• Bachelor’s degree in Life Sciences / Pharmacy / Biotechnology or related disciplineExperience• Freshers or candidates with 0–2 years of experience in clinical research, healthcare operations, or customer supportSkills• Strong written and verbal communication skills• Basic understanding of clinical trial processes (preferred)• Proficiency in MS Office and database systems• High attention to detail and strong organizational skills• Ability to manage multiple tasks and meet timelinesAbout the OrganizationLabcorp – A global leader in clinical research and laboratory services, offering strong exposure to global clinical trial operations, investigator support, and long-term career growth in clinical operations.
Roles & Responsibilities• Review clinical study reports, patient safety narratives, appendices, informed consent forms, clinical protocols, and amendments for accuracy, clarity, and consistency• Ensure documents align with source data, templates, client requirements, and regulatory standards• Provide detailed review comments and documentation feedback to Medical Writers• Complete document reviews and QC checklists within agreed timelines• Collaborate with writers to resolve discrepancies, omissions, and errors• Understand assigned tasks and adhere to budgeted hours• Participate in staff, client, and project update meetings as required• Review and support updates to departmental templates• Perform additional duties as assigned by Manager or SupervisorQualification• Associate degree or Bachelor’s degree (B.Pharm/ BS / BA)• Relevant and equivalent experience may be considered in lieu of formal educationExperience• Minimum 3 years of clinical research experience• At least 3 years at Associate Medical QC Editor levelSkills• Excellent command of written and spoken English• Strong knowledge of editing and proofreading conventions, grammar, and style• Understanding of medical, pharmacokinetic, and statistical principles• High attention to detail and document accuracy• Knowledge of medical terminology (preferred)• Proficiency in MS Word, Excel, and PowerPointAbout the OrganizationFortrea – A global clinical development and patient access solutions company delivering high-quality regulatory and clinical documentation, with flexible remote opportunities and strong professional growth in medical writing and quality review.
Roles & Responsibilities• Support Medical Writing activities including appendices collation, peer review, QC, and document publishing for assigned projects• Assist in preparation of study-related documents such as Study Protocols, Clinical Study Reports (CSRs), and Patient Narratives• Prepare Clinical Study Report Appendices as per ICH E3 Section 16• Support publishing of documents within the Medical Writing department and cross-functional teams as per agreed processes• Track timelines and communicate document status to Medical Writers, Project Managers, and Clients• Assist in document review and QC activities within Medical Writing• Ensure compliance with Fortrea or Sponsor SOPs, ICH-GCP, and applicable regulatory guidelines• With guidance from senior staff, prioritize preparatory tasks and ensure deadlines are met• Perform additional duties as assigned to support project deliveryQualification• Bachelor’s degree in Biomedical / Life Sciences or related discipline• Relevant and equivalent experience may be considered in lieu of formal educationExperience• 2–3 years of relevant experience or equivalent combination of education and experience• Prior experience as a Publisher within a Medical Writing or Clinical department for national or multinational studiesSkills• Strong understanding of clinical research documentation and publishing processes• Knowledge of ICH-GCP and regulatory requirements• Excellent written and verbal communication skills in English• Good organizational, coordination, and time-management skills• Ability to manage multiple tasks and meet timelinesWork Environment• Home-based / remote working environment• Ability to work on a computer for extended periods (6–8 hours)• Regular sitting and use of hands for keyboard and document handling• Adequate visual and auditory capability to meet job requirementsAbout the OrganizationFortrea – A leading global provider of clinical development and patient access solutions, offering opportunities to work on global clinical research projects in a flexible, remote work environment.
Roles & Responsibilities• Support oligonucleotide synthesis and production processes• Perform SOP-based laboratory operations and maintain accurate documentation• Assist in QA/QC procedures and manufacturing workflows• Handle routine laboratory tasks to ensure smooth production cycles• Collaborate with team members to meet quality, productivity, and timeline standardsQualification• M.Sc or Btech in Life Sciences / Biotechnology / Biochemistry or related disciplinesExperience• Freshers onlySkills• Strong interest in laboratory operations and biotech production environments• Good attention to detail and documentation practices• Willingness to learn oligonucleotide chemistry and lab management• Team-oriented mindset with basic understanding of quality processesAbout the OrganizationBarcode Biosciences – A Bangalore-based genomic services company focused on innovative DNA-based solutions, offering hands-on exposure and growth opportunities in oligonucleotide production and life sciences manufacturing.
ROLES & RESPONSIBILITIES:• Conduct comprehensive assessments of patients’ physical conditions, medical history, and individual needs• Develop and implement personalized, goal-oriented treatment plans focused on rehabilitation and pain management• Deliver virtual physiotherapy sessions through the company’s mobile health app• Monitor patient progress and modify treatment plans to ensure optimal outcomes• Educate patients on exercises, self-care techniques, and lifestyle modifications• Collaborate with healthcare professionals to provide coordinated and comprehensive care• Maintain accurate digital records of patient assessments, treatments, and progress reports• Stay updated with the latest advancements in physiotherapy, healthcare technology, and treatment methodsQUALIFICATION:• Bachelor’s or Master’s Degree in Physiotherapy• Licensed and Registered PhysiotherapistEXPERIENCE:• Minimum 2 years of clinical experience• Experience in home-based care is preferredSKILLS:• Strong physiotherapy and rehabilitation expertise• Excellent communication and interpersonal skills• Clinical assessment and treatment planning abilities• Tech-savvy with the ability to use mobile health applications• Ability to work independently and within a healthcare team• Patient-focused approach with strong problem-solving skillsBENEFITS:• Provident Fund• Access to advanced healthcare technology• Collaborative and dynamic work environmentABOUT THE COMPANY:Lifetime Health Plus Care Pvt Ltd is an innovative home healthcare company that uses advanced technology to deliver personalized and convenient medical services. Through its mobile app, the company connects patients with experienced healthcare professionals, ensuring accessible and high-quality care. Lifetime Health is dedicated to enhancing patient well-being by bringing professional healthcare services directly to patients’ homes.
Roles & Responsibilities• Interpret clinical trial protocols and design study calendars• Develop and manage site budgets aligned with CTAs and sponsor requirements• Ensure protocol, budget, and documentation accuracy and compliance• Collaborate with cross-functional clinical operations teams• Maintain study documentation and support operational readiness• Support clinical trial execution activities across study lifecycleQualification• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related fieldExperience• 1–5 years of experience in one or more of the following:– Clinical Research Coordinator (CRC)– Clinical Research Associate (Site level)– Clinical Data Management– Pharmacovigilance– Records ManagementSkills• Good understanding of clinical trial processes• Strong analytical and problem-solving skills• Effective written and verbal communication• Attention to detail and documentation accuracy• Ability to work collaboratively in cross-functional teamsAbout the OrganizationAdvarra is a global leader in clinical research technology and services, supporting safer, smarter, and more efficient clinical trials to improve patient outcomes worldwide.
Role & Responsibilities• Manage and review adverse event data ensuring accuracy, consistency, and regulatory compliance• Apply clinical judgment and regulatory knowledge to safety case processing• Process safety reports from clinical trials, spontaneous reports, literature, PSPs, and market research• Perform MedDRA coding, seriousness, causality, and listedness assessments• Identify data gaps and conduct follow-ups with investigators, HCPs, and patients• Ensure compliance with global expedited reporting requirements including FDA, EMA, MHRA, and PMDA• Work with global safety systems such as MOSAIC and LSS• Collaborate with cross-functional and global pharmacovigilance teams• Support literature search strategies and safety workflow improvements• Maintain awareness of pharmacovigilance agreements and regulatory commitmentsQualification• Master’s Degree in Pharmacy, Life Sciences, Biological Sciences, or HealthcareExperience• 4–8 years of experience in Pharmacovigilance or Drug Safety• Hands-on experience in adverse event management and regulatory reporting• Exposure to global safety operations and electronic PV systemsSkills• Strong understanding of global pharmacovigilance regulations• Excellent critical thinking and problem-solving abilities• Proficiency in safety databases and case processing systems• Strong written and verbal communication skills in English• Ability to work effectively in global, cross-cultural teamsAbout the Company• Eli Lilly and Company is a leading global pharmaceutical organization, Known for life-changing innovations and patient-centric healthcare solutions, Operates extensive global drug safety and regulatory programs.
ROLE & RESPONSIBILITIES:• Conduct comprehensive assessments of patients’ physical conditions, medical history, and rehabilitation needs• Develop personalized, goal-oriented treatment plans focusing on recovery, pain management, and overall well-being• Deliver virtual physiotherapy sessions through the company’s mobile health app• Monitor patient progress and modify treatment plans to ensure optimal outcomes• Educate patients on exercises, self-care techniques, and lifestyle modifications• Collaborate with healthcare professionals to provide coordinated and holistic care• Maintain accurate digital records of assessments, treatments, and progress reports• Stay updated with the latest advancements in physiotherapy, healthcare technology, and treatment practicesQUALIFICATION:• Bachelor’s or Master’s degree in Physiotherapy from a recognized institution• Licensed and registered PhysiotherapistEXPERIENCE:• Minimum 2 years of clinical experience required• Experience in home-based care is an added advantageSKILLS:• Strong clinical and physiotherapy expertise• Excellent communication and interpersonal skills• Tech-savvy with the ability to use mobile health applications• Ability to work independently and within a multidisciplinary team• Patient-focused approach with strong organizational skillsABOUT THE COMPANY:Lifetime Health Plus Care Pvt Ltd is an innovative home healthcare company dedicated to delivering personalized and convenient medical services. By leveraging advanced technology and a user-friendly mobile app, the organization connects patients with experienced healthcare professionals to provide seamless, high-quality care at home. Lifetime Health is committed to enhancing patient well-being through accessible, technology-driven healthcare solutions.
Roles & Responsibilities• Conduct detailed inspections of studies involving animal test systems to ensure compliance with Good Laboratory Practice (GLP) principles• Provide continuous support to study teams to maintain GLP compliance throughout study execution• Review draft and final Safety Assessment study reports for accuracy, completeness, and regulatory compliance• Verify that study methods, procedures, observations, and results are accurately documented and aligned with raw data• Ensure adherence to regulatory and internal quality standards across preclinical safety studies• Support quality audits and inspection readiness activities• Identify quality gaps and assist in implementation of corrective and preventive actions (CAPA)Qualification• M. Sc in Life Sciences, Zoology, Toxicology, or related discipline (Mandatory)Experience• 1–2 years of hands-on experience in GLP Quality Assurance• Prior experience working in a Contract Research Organization (CRO) preferredSkills• Strong understanding of GLP guidelines and regulatory quality standards• Knowledge of preclinical safety assessment and animal study compliance requirements• Excellent documentation review and analytical skills• Strong attention to detail with high accuracy levels• Good communication and teamwork skills• Ability to work in a fast-paced CRO environmentAbout the OrganizationEurofins Advinus is a leading Contract Research Organization providing integrated preclinical, clinical, and bioanalytical research services. Known for its strong regulatory compliance and scientific expertise, the organization supports global pharmaceutical and biotechnology companies in advancing safe and effective therapies.
Roles & Responsibilities• Coordinate and deliver Global Clinical Solutions (GCS) services ensuring lifecycle management and business continuity for projects, services, and technology• Provide expert user support including conducting system/process/tool training and facilitating knowledge sharing across teams• Establish guidelines, protocols, and communication frameworks with cross-functional collaborators• Analyze processes, tools, and systems to identify opportunities for efficiency improvement and risk reduction• Lead and manage continuous improvement projects using lean principles including planning, prioritization, execution, and delivery tracking• Support implementation of organizational and functional changes to enhance performance and operational efficiency• Monitor program performance, evaluate effectiveness, and recommend corrective actions when required• Train and mentor teams in continuous improvement methodologies and change adoption• Develop and maintain knowledge management frameworks to capture and reuse organizational learning• Act as a subject matter expert in one or more GCS domains and guide protocol development and standards• Contribute to business continuity planning and service optimization across global clinical operationsQualification• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Clinical Research, Business Administration, or related disciplineExperience• Experience in clinical development, clinical operations, or clinical technology platforms• Hands-on experience in lifecycle management, service delivery, and business continuity planning• Experience leading continuous improvement or transformation projects• Exposure to regulated environments and quality systems (GxP) preferredSkills• Strong knowledge of lean improvement methodologies (Lean / Six Sigma preferred)• Expertise in process improvement, risk management, and change implementation frameworks (e.g., Prosci/ADKAR preferred)• Ability to design and deliver training programs and user support initiatives• Strong stakeholder and collaborator management across global matrix environments• Experience developing performance dashboards, KPIs, and benefits tracking metrics• Knowledge of knowledge management tools and continuous improvement frameworks• Strong analytical, communication, and leadership skills with focus on scalable solutionsAbout the OrganizationAstraZeneca is a global, science-led biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines. By combining science, technology, and collaborative thinking, the organization accelerates clinical development and improves patient outcomes while fostering a culture of continuous learning and innovation.