2398 Pharmacy Jobs - Page 42

Detailed job description - Skill Set: Technically strong hands-on Self-driven Good client communication skills Able to work independently and good team player Flexible to work in PST hour(overlap for some hours) Past development experience for Cisco client is preferred.

Role & responsibilities: Designation: Executive/Sr. Executive Role: Retail - Pharmacist Department : B&M Retail Location : Ranchi Salary : upto 3 LPA What You'll Do: Dispense medications as per doctors' prescriptions. Manage inventory to meet market demands. Ensure compliance with patient confidentiality and scheduled drug regulations. Communicate tactfully to meet business needs. What Were Looking For: Bachelor's degree or Diploma in Pharmacy. Free Registration from State Pharmacy Council. Strong customer service and communication skills. Analytical abilities and proficiency in computer applications. About Tata 1mg: Tata 1mg is a trusted health partner for end consumers and large institutions. Our Mission is to make healthcare understandable, accessible, and affordable for all Indians. Over the past three years, we've worked to build a healthcare platform that guides customers to the right and affordable care. Today, Tata 1mg is present in 1000+ cities And were just getting started. Leading the chart as one of the top consumer health platforms through ePharmacy, eDiagnostics, e-consult and offline stores, Tata 1mg has delivered over 15M ePharmacy orders, 2M eDiagnostics orders & 1M+ organic users/day in 2022 and we are just getting started. Our strongest asset is our 6400+ people enabling us to deliver on our mission consistently. Know more about us: https://www.1mg.com/aboutUs Kindly share your resume at rachna.singh@1mg.com Ansh - 9289567981 Role: Retail Store Manager Industry Type : Pharmaceutical & Life Sciences Department: Heathcare and life science Employment Type: Full Time, Permanent Role Category : Retail Store Operations UG: B.Pharma in Pharmacy, Diploma in Any Specialization

We are looking for young people with a strong aptitude for sales and marketing for the role of Medical Representatives. Medical Representatives are our link to our customers. Their role is to engage, educate and enable members of the medical community with regards to our products. Science/Pharmacy: Fresh Graduates below 23 years of age or individuals below 25 years of age with relevant experience in pharma can apply. Experience: Up to 1 year in Pharmaceutical Sales Posted Date: 08/07/2025

The Researcher of Preclinical (Toxicology and Biocompatibility) in this role will apply expertise in toxicology and medical device biocompatibility testing including development of toxicity study design and biocompatibility testing design for drug/drug packaging system/medical device development, monitoring the studies, and development of toxicological risk assessments. The successful candidate will have hands-on experience in hazard evaluation of chemicals used in manufacturing and will participate preparing reports for external regulatory bodies in accordance with ICH and ISO10993-17. This is an opportunity to become part of a highly matrixed multidisciplinary team that is responsible for ensuring the safety of both drugs and medical devices for Peritoneal dialysis, Hemodialysis, and Acute therapies. Essential Duties and Responsibilities: Assist or work independently in designing, planning, monitor various GLP toxicity studies, biocompatibility studies, and qualification of impurities with some supervisions from direct manager and senior members of the organization. Assist or work independently as an author for toxicological risk assessment reports on leachables, extractables, residual solvents and excipients and review or concur toxicology assessment reports as subject matter expert (SME) in accordance with ICH and ISO10993-17. Work independently on hazard evaluation of chemicals used in manufacturing and issuing safety data sheet (SDS). Participate as preclinical/toxicology representative and contribute in core technical team meetings as SME and provide inputs and lead task to be executed for completion of projects with effective collaboration and deliverables. Participate in change control management and impact assessment. Propose options, work closely with stakeholders and develop action plans for problem-solving, product and process improvement. Prepare and/or review nonclinical eCTD and PBRER sections. Utilize in silico tools to assess toxicological endpoints. Qualifications The position requires relevant technical knowledge in toxicology and biocompatibility testing. Demonstrated ability to understand and apply global regulatory guidelines including OECD and FDA GLP, ICH Q3 guidelines, ISO 10993. Excellent oral and written communication in English language. Utilize a logical, methodical approach when problem solving, developing solutions and making recommendations. Ability to work independently and prioritize assignments to meet project schedules. Ability to design experiments, monitor toxicology studies, interpret the results and draw meaningful conclusions from the data and prepare reports for external regulatory bodies Education and/or Experience: Master of Life Sciences / Veterinary / Biotechnology / Pharmacy (or relevant) with 4-6 years of relevant work experience, or PhD with relevant experience during thesis (&/or Post-doc) e.g., in in vitro and in vivo pharmacological (preferably sterile injectable/parenteral formulations) and toxicological studies and risk assessment of chemicals, biocompatibility testing of medical devices, drug packaging system. Skills: Demonstrated ability in clear and effective communication (written, oral) and presentation skills to global stakeholders, Fluency in English. Can effectively communicate with internal and external customers. Solid computer skills : email, good documentation practice, and collaboration tools: e.g., Zoom, Teams, Microsoft Office products, etc. Demonstrated ability to work in a matrix environment with multiple stakeholders Demonstrates flexibility and the ability to shift gears between projects comfortably. Proven ability to deliver results by owning & being accountable for budget, timeline, and product/project deliverables.

is introduced by Government of Jharkhand, initiative aims to empower youth and create employment through skill-based pharmaceutical training at the grassroots level. Responsibilities Conduct offline/online training for rural candidates Deliver curriculum related to basic pharmacy, medicine handling, and store operations Monitor trainees learning progress and performance Evaluate assessments and maintain training records Provide hands-on demonstrations and practical exposure Ensure alignment with government scheme guidelines Jharkhand Government Job Location Base Salary Per year Education Degree /Certification in D-Pharma/ B-Pharma Good communication in Hindi and regional language Preference given to candidates with rural outreach experience Skills Strong knowledge of pharmaceutical subjects Teaching and training ability Good communication skills (Hindi & regional language) Curriculum planning and delivery Practical knowledge of medical store operations Position: Pharma Faculty Thank you for submitting your application. We will contact you shortly!

About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About the role DNV Product Assurance AS is one of the leading Notified Bodies for IVD medical devices. The unit is entitled to carry out tasks related to conformity assessment of IVD medical devices with Regulation (EU) 2017/746 In Vitro Medical Devices before such products are placed on the market. The role of Clinical Assessor is to assess performance data supporting safety and performance of IVD medical devices. Main tasks in this role are: Performing assessment and preparing reports of clinical performance aspects of legal manufacturers technical documentation according to the requirements given in the Regulation (EU) 2017/746. Evaluation of the summary of safety and performance reports for high-risk IVD medical devices. Review and approval of performance evaluation report and other relevant performance documentation for accuracy and compliance with the requirements in the Regulation (EU) 2017/746. Education and Competencies required: Clinical Assessors shall have a technical college degree in a relevant product or medical area, as described below. Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology What we offer A competitive compensation and benefit package DNV training and qualification program A professional community in a prestigious technological company Possibilities to work with interesting and challenging projects Access to an extensive competence network Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. About you Candidates must have a minimum 4 years work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the Assessment of Performance evaluation data, including Scientific Validity and Clinical Performance, or conducting performance evaluation studies for IVD devices. A PhD in a relevant area for IVD medical devices can substitute 3 years of work experience provided that it includes 2 years experience in Performance evaluation. Personal Qualities: Analytical approach. Strong communication skills. Customer focus. Excellent reporting skills. Ability to work independently and efficiently. Ability to form recommendations on certification in complex cases.

Qualification: D. Pharma or B. Pharma. Registration: Haryana Pharmacy Council Experience: 3-8Years Must have worked in IP& OPD Pharmacy Contact: HR Department Email : www.umkalhospital.com Mo. : 8860077509,7988561761

Conduct research and development in pharmaceutical analytics. Develop and implement R&D strategies and plans. Monitor and analyze R&D performance and trends. Prepare R&D reports and presentations. Collaborate with other teams to achieve R&D objectives. Provide training and support to junior R&D scientists. Stay updated with the latest R&D trends and best practices.

We are seeking a highly motivated and detail-oriented Pharmacist to join our team as a Medical Records Specialist. In this role, you will play a crucial part in ensuring the accuracy, completeness, and confidentiality of patient medical records, with a focus on medication-related information. You will collaborate with healthcare professionals, patients, and other stakeholders to maintain high-quality records that support safe and effective patient care. Responsibilities: Review and analyze patient medical records to identify medication-related issues, discrepancies, or potential drug interactions. Ensure accurate documentation of medication history, allergies, and adverse reactions. Collaborate with physicians, nurses, and other healthcare providers to clarify medication orders and resolve any discrepancies. Maintain up-to-date knowledge of relevant regulations and guidelines related to medical record keeping and patient privacy (HIPAA). Contribute to quality improvement initiatives by identifying trends, patterns, or areas for improvement in medication-related documentation. Provide education and training to healthcare professionals on proper documentation practices and medication safety. Respond to inquiries from patients, healthcare providers, and other stakeholders regarding medication-related information in medical records. Qualifications: Doctor of Pharmacy (Pharm.D.) degree from an accredited institution. Strong understanding of medical terminology, pharmacology, and drug interactions. Excellent attention to detail and ability to maintain accuracy in record keeping. Strong communication and interpersonal skills to effectively collaborate with healthcare professionals and patients. Knowledge of relevant regulations and guidelines related to medical record keeping and patient privacy (HIPAA). Ability to work independently and as part of a team. Proficiency in using electronic health record (EHR) systems and other relevant software. Preferred Qualifications: Experience in medical record review or clinical pharmacy practice. Certification in a relevant area, such as medication therapy management or informatics. WhatsApp / Phone : 9840020085

Job Description Position: Medical Coder Ct: HR DEEPA 7305649640 You have at least a Diploma/Degree in any field. This role is open to fresh graduates with excellent English communication skills. You pay strong attention to details and are capable of delivering top-quality work You are goal-oriented and thrive in fast-paced environments Maintains a working knowledge of CPT-4, ICD-10-CM, and ICD-10-PCS coding principles, governmental regulations, UHDDS (Uniform Hospital Discharge Data Set) guidelines, AHA coding clinic updates, and third-party requirements regarding coding and documentation guidelines

Company Description Heureka Medihealth's vision is to advance the standard and quality of healthcare across clinical diagnostics, pharmaceuticals, and medical education technology segments. The company is committed to innovation and excellence in the healthcare sector, providing top-notch services and products. Heureka Medihealth aims to improve patient outcomes and contribute substantially to the medical field's growth and development. Role Description This is a full-time on-site role for a Medical Sales Representative at Heureka Medihealth, located in Aurangabad. The Medical Sales Representative will be responsible for promoting and selling medical products and services to healthcare professionals and institutions. Day-to-day tasks include identifying sales opportunities, maintaining customer relationships, providing product information, and achieving sales targets. The role also involves making presentations, negotiating contracts, and attending medical conferences and meetings to stay updated with industry trends. Qualifications Experience in Medical Sales and a proven sales track record Strong Communication and Customer Service skills Knowledge of Medicine and Pharmacy Ability to work effectively in a team and independently Bachelor's degree in a relevant field such as Life Sciences, Pharmacy, or Business Excellent organizational and time management skills Willingness to travel as required for the role,

Responsibilities: * Dispense medications accurately and efficiently * Collaborate with healthcare team on patient care plans * Provide expert advice on drug usage and safety * Manage pharmacy inventory and ordering process

Increase brand awareness and build a relationship with prospective and existing customers Ensure that proper advertising and marketing are done through the medical product sales Liaison with doctors, hospitals and medical staff

Division Department Sub Department 1 Job Purpose Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets Key Accountabilities (1/6) Execute production activities in a shift by managing available resources to achieve production target Execute assigned tasks as per planned production activity to meet production targets for a shift Regulate usage of consumables in the production process at optimum levels to save costs Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area Key Accountabilities (2/6) Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality Ensure all operations are performed as per GMP & Safety norms by reviewing all processes and documents for compliance Ensure equipment, facility and block premises are maintained as per regulatory compliance Maintain system integrity by updating documentations and deviations on CipDox while performing operations Perform validation, qualification and calibration as per schedule and update output of all activities in the systems Prepare new documents and update existing documents as per GMP requirement Key Accountabilities (3/6) Prepare manufacturing records and update online documentation to meet production and cGMP requirements Maintain online documentation and timely entries in BMR and supporting documents Prepare new documents and update existing documents as per GMP requirement Operate software such as SAP, CipDox and QMS Key Accountabilities (4/6) Follow safe work processes and ensure safety appliances are utilised during production activities in shifts to create a safe working environment Ensure safety systems and procedures followed by the operators in the shift Ensure availability and usage of PPEs in the shift by coordinating with HSE department for requirements and shift schedule Key Accountabilities (5/6) Execute production activities in a shift by managing available resources to achieve production target Execute assigned tasks as per planned production activity to meet production targets for a shift Regulate usage of consumables in the production process at optimum levels to save costs Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area Key Accountabilities (6/6) Major Challenges Meeting shift targets due to unavailability of adequate resources. Overcome by efficient work load distribution and resource optimisation Meeting production targets due to lapses in knowledge transfer between shifts. Overcome by bridging gaps between inter-shift communication Maintaining cGMP requirements during system downtime. Overcome by coordinating with the engineering team and technical support team Key Interactions (1/2) QA/QC for scheduling of batches, issues in product (Daily) Engineering & Utility for system related queries (Daily) Formulation Technical Support for troubleshooting in products (Case Basis) Formulation Technology Transfer for support in new products (Project Basis) Stores and Warehouse for RM/PM related activities (Daily) Safety for safety rounds and PPE requirement (Daily) Key Interactions (2/2) Maintenance Contractor and vendors for any machine repairs and spares (Case Basis) Equipment manufacturer: For troubleshooting in machine (Case Basis) Dimensions (1/2) Direct Reports : 12 (dotted reporting in shift) Number of areas managed : 3 Number of dosage forms : 2 Number of tech transfer supported per month : 2 Number of batches executed per month : 35-40 Achieve internal OTIF more than 90% YOY improvement in shift operations efficiency Achieve Zero reportable accidents / incidences during manufacturing Achieve set target for batch failure reduction Achieve 0% errors in online documentation Meet 100% compliance to SOP and safety regulations Dimensions (2/2) Key Decisions (1/2) Resource allocation for each shift Workload distribution in each shift Key Decisions (2/2) Up-gradation in Facility and Documents (To Section Head) Modification in plant and equipment (To Section Head) Deviation and implementation of CAPAs (To Section Head) Education Qualification Bachelor in Pharmacy Relevant Work Experience 3-4 years of experience with 2 years of experience in pharmaceutical manufacturing Knowledge of cGMP practices, equipment operations required for Formulation Production

Job Description Designation: Pharmacist Role: QC Pharmacist Department: Warehouse Operations Location: Bangalore/Chennai / Mumbai About Tata 1mg Tata 1mg is a trusted health partner for end consumers and large institutions. Our Mission is to make healthcare understandable, accessible, and affordable for all Indians. Over the past three years, we've worked to build a healthcare platform that guides customers to the right and affordable care. Today, Tata 1mg is present in 1000+ cities And were just getting started. Leading the chart as one of the top consumer health platforms through ePharmacy, eDiagnostics, e-consult and offline stores, Tata 1mg has delivered over 15M ePharmacy orders, 2M eDiagnostics orders & 1M+ organic users/day in 2022 and we are just getting started. Our strongest asset is our 6400+ people enabling us to deliver on our mission consistently. Know more about us: https://www.1mg.com/aboutUs Brief about the Team The warehouse operations team is within the supply chain vertical of Tata 1mg. The team works closely with the org-wide leadership team, business, product, growth, and category teams to drive operational excellence and strategic initiatives. The team works on special projects and innovations that aim to deliver high impact. The projects span across business verticals including e-pharma, e- diagnostics, and retail. What will you do What will you do Customer Support Read & validate prescriptions (Rx) + OTC orders Contact customers for clarification or information required to process the order - Situational requirements Inventory Management & Order Processing management Responsible for physically performing order picking, quality checks, packing and handover to the riders Ensure all orders are processed within the defined cut-off TAT (Turnaround Time) Responsible for physically performing stock receiving and put away processes Conduct daily stock audits and ensure accountability for inventory shrinkage Follow up and ensure timely closure of pullout and purchase returns Ensure customer satisfaction through timely order fulfillment, issue resolution, and excellent service Compliance Ensure strong quality checks while packing/ dispensing medicines Ensure 100% compliance per the process guidelines What we are looking for 1 + years of relevant experience (pharmacist Diploma or Bachelor (D. Pharma or B. Pharma License for that state. Should be comfortable working in shifts and on weekends Why Join Us? Tata 1mg provides one of the most exciting and high-growth environments to work. You get the added benefit of working in a prestigious legacy brand like Tata and a highly dynamic and versatile startup like 1mg. Being an integral part of the Warehouse Operations will provide you to closely work with the Operations and Logistics team which is spread PAN India.

PRESCRIPTION HANDLING, STOCK MANAGEMENT, PURCHASE & SALES REPORT.

Long Description 1 Exposure of execution of planning of Inprocess, Finished product, stability and cleaning validation samples of MDI / DPI formulation. 2 Exposure of compliance to all cGMP, GxP or any other regulatory requirements, including EHS requirements. 3 Maintenance of GLP in the Laboratory. 4 Having knowledge of Analytical Instruments like HPLC, GC, GCMS, LCMS, UV, IR, KF, ACI, NGI, DUSA, Spray Pattern etc. 5 Exposure of Laboratory investigation like OOS, OOT, Incidence, Deviation, CAPA, Change control etc. 6 Exposure of Stability sample management & Regulatory Audits. 7 Exposure of Analytical method transfer, Analytical method validation / Verification activity. 8 Exposure of Calibration of Analytical Instruments & Equipment’s 9 Compliance to observation noted during internal and external audits. Competencies Strategic Agility Process Excellence Collaboration Innovation & Creativity Result Orientation Stakeholder Management Customer Centricity Developing Talent Education Graduation in Pharmacy Work Experience 10 to 15 years.

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy/BSc. Nursing Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases.Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. What are we looking for Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines. Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualification Bachelor of Pharmacy,Master of Pharmacy,BSc. Nursing

Position: Medical Coder HR Kamatchi 8925264660 Job Description: Designation :Medical Coder Trainee/ Medical Coder/Sr.Medical Coder/Team leader/ Medical Coding Analyst Specialization :Surgery/Observation/ E&M/ In_Patient/ Out Patient/Multi specialty/ ED Requirement : Experience in Medical Coding (or)Knowledge in Anatomy and Physiology. Must possess Good Written & Verbal Skills Basic Computer Skills. Candidate should be from Any Life Science, Paramedical, Medical Graduates and Post Graduates Salary : Negotiable (Incentives & Benefits as per Corporate Standards) Hiring Process :Face to Face Interview, Telephonic Interview Benefits: 1. Pick Up & Drop Facility 2. Food Facility 3. Day Shift 4. Easily Accessible to Job 5. Weekend Off Career Growth: Excellent opportunity to enhance your career by getting CPC(Certified Association of Professional Coders) and AHIMA(American Health Information Management Professional Coders) and CCS(Certified Coding Specialist) Certification from AAPC(American Association) respectively. Placement Locations: Chennai Contact Details: Achievers Spot 13, Ramanathan Street,2nd Floor, T.Nagar, Chennai 600017 Landmark: Adjacent to Ranganathan Street Ph: 8925264660 , 9566157627/9566133256/9566284629/9566157632/9840708203 Email: hr@achieversspot.com Website: www.achieversspot.com HR Kamatchi 8925264660 Achievers Spot

Position: Medical Coder Ct:HR BHAVANI - 9566284629 We are looking for a Medical coder Job role Make sure that codes are assigned correctly Complying with medical coding guidelines and policies Receiving and reviewing patients charts and documents for verification and accuracy Recruitment Process: Should have good knowledge in Medical coding Should be Certified Medical Coder Should have good communication skills Immediate joiners are needed Job Type: Full-time Salary: 15,000.00 - 23,000.00 per month Ct Us: HR BHAVANI 9566284629 Job Type: Full-time

JD: Following strict coding guidelines within established productivity standards. Addressing coding related inquires for providers as needed, U.S. only. Attending meetings and in-service training to enhance coding knowledge, compliance skills, and maintenance of credentials. Maintaining patient confidentiality. Candidates should have Good Communication & Analytical Skills and should be Good at Medical Terminology (Physiology & Anatomy). * Should be a good team player with good attitude. * Should be flexible to work in rotational shifts whenever required *Ready to Join with us immediately. Contact Details: Achievers Spot 13, Ramanathan Street,2 nd Floor, T.Nagar, Chennai – 600017 Landmark: Adjacent to Ranganathan Street Ct: HR Bhavani Ph:9566284629 Email: bhavani@achieversspot.com

About The Role Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Analyst Qualifications: MSc/Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 3 to 5 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.A critical phase in clinical research that assures collection, integration and availability of data at appropriate quality and cost. It also supports the conduct, management and analysis of studies across the spectrum of clinical research as defined by the National Institutes of Health (NIH). What are we looking for Ability to establish strong client relationshipAbility to handle disputesAbility to manage multiple stakeholdersAbility to meet deadlinesAbility to perform under pressure Roles and Responsibilities: In this role you are required to do analysis and solving of lower-complexity problems Your day to day interaction is with peers within Accenture before updating supervisors In this role you may have limited exposure with clients and/or Accenture management You will be given moderate level instruction on daily work tasks and detailed instructions on new assignments The decisions you make impact your own work and may impact the work of others You will be an individual contributor as a part of a team, with a focused scope of work Please note that this role may require you to work in rotational shifts Qualification MSc,Bachelor of Pharmacy,Master of Pharmacy

Brief Position Description: Novotech continues to expand its global commercial capabilities and is seeking a Senior Sales Enablement Analyst for its Bangalore office. This strategic role will support the Business Development team, driving sales lead generation efforts, insights, and analysis to enhance decision-making and contribute to Novotech s continued growth and market leadership. Core responsibilities: Reporting to a Lead Analyst, the Sales Enablement Analyst will: Account-Based Marketing (ABM) Develop and execute personalized marketing strategies targeting high-value accounts. Align marketing efforts with sales teams to enhance engagement and conversion rates. Utilize data-driven insights to optimize account selection and prioritization. Lead Management Identify, nurture, and qualify potential leads to maintain a healthy lead Management Implement lead scoring models to assess prospect readiness and prioritize outreach. Track and analyze lead engagement to refine marketing strategies. Create Dynamic and Static lists for buying Journey and Call to Actioned Marketing Databases Management & Enrichment Maintain and update marketing databases to ensure accurate and actionable data. Conduct data cleansing, enrichment, and segmentation for targeted campaigns. Integrate various data sources (Salesforce, ZoomInfo, Global Data, etc.) for comprehensive insights. Implement the data compliance rule: GDPR Reporting & Analytics Generate detailed reports for Sales Meeting, lead generation, and pipeline health, Executive summary. Provide data-driven recommendations to optimize marketing and sales strategies. Collaborate with stakeholders to present actionable insights from reporting tools. Marketing Insights & Competitive Intelligence Funding Analysis: Track funding trends and investment activities to identify potential opportunities. Pipeline & Milestone Analysis: Monitor key industry projects, product launches, and development phases. Conference Intelligence: Gather insights from industry events, webinars, and networking opportunities. Intent Data Utilization: Leverage behavioral signals to predict buyer intent and target prospects effectively. Mergers & Acquisitions (M&A) Tracking: Assess M&A activities to uncover new business opportunities. Patient Recruitment Challenges: Analyze challenges in clinical trial recruitment and provide strategic solutions. Financial Results Review: Monitor quarterly and annual financial reports for strategic decision-making. Phase Pull-Through: Track drug development phases to anticipate upcoming market needs. Required Qualification(s): Preferred : Degree in Life Science or related field (Pharmacy, Medical, Biology), MBA, Data Science, Business Analytics Acceptable : Undergraduate degree in a business/administrative and information technology related courses of study. Required Professional Experience: 5+ years in sales enablement, business development support, inside sales, or sales operations Required skills: Advanced Microsoft office capabilities and Excel in particular Advanced LinkedIn capabilities. Knowledge of LinkedIn Sales Navigator would be a plus. Excellent oral and written communication and ability to engage, manage, and communicate effectively with stakeholders at all levels of the organization. Strong analytical skills and and proven ability to analyze and interpret internal and external data to generate strategic insights. Attention to detail and accuracy in execution. Self-motivated with the ability to work independently and take initiative Experience with any programming language such as SQL, Python, R Experience with any data visualization tools Salesforce Analytics/ Tableau / Power BI Experience with CRM & Marketing Automation: Salesforce, Pardot or HubSpot, ZoomInfo Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs. We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities. We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application. Brief Position Description: Novotech continues to expand its global commercial capabilities and is seeking a Senior Sales Enablement Analyst for its Bangalore office. This strategic role will support the Business Development team, driving sales lead generation efforts, insights, and analysis to enhance decision-making and contribute to Novotech s continued growth and market leadership. Core responsibilities: Reporting to a Lead Analyst, the Sales Enablement Analyst will: Account-Based Marketing (ABM) Develop and execute personalized marketing strategies targeting high-value accounts. Align marketing efforts with sales teams to enhance engagement and conversion rates. Utilize data-driven insights to optimize account selection and prioritization. Lead Management Identify, nurture, and qualify potential leads to maintain a healthy lead Management Implement lead scoring models to assess prospect readiness and prioritize outreach. Track and analyze lead engagement to refine marketing strategies. Create Dynamic and Static lists for buying Journey and Call to Actioned Marketing Databases Management & Enrichment Maintain and update marketing databases to ensure accurate and actionable data. Conduct data cleansing, enrichment, and segmentation for targeted campaigns. Integrate various data sources (Salesforce, ZoomInfo, Global Data, etc.) for comprehensive insights. Implement the data compliance rule: GDPR Reporting & Analytics Generate detailed reports for Sales Meeting, lead generation, and pipeline health, Executive summary. Provide data-driven recommendations to optimize marketing and sales strategies. Collaborate with stakeholders to present actionable insights from reporting tools. Marketing Insights & Competitive Intelligence Funding Analysis: Track funding trends and investment activities to identify potential opportunities. Pipeline & Milestone Analysis: Monitor key industry projects, product launches, and development phases. Conference Intelligence: Gather insights from industry events, webinars, and networking opportunities. Intent Data Utilization: Leverage behavioral signals to predict buyer intent and target prospects effectively. Mergers & Acquisitions (M&A) Tracking: Assess M&A activities to uncover new business opportunities. Patient Recruitment Challenges: Analyze challenges in clinical trial recruitment and provide strategic solutions. Financial Results Review: Monitor quarterly and annual financial reports for strategic decision-making. Phase Pull-Through: Track drug development phases to anticipate upcoming market needs. Required Qualification(s): Preferred : Degree in Life Science or related field (Pharmacy, Medical, Biology), MBA, Data Science, Business Analytics Acceptable : Undergraduate degree in a business/administrative and information technology related courses of study. Required Professional Experience: 5+ years in sales enablement, business development support, inside sales, or sales operations Required skills: Advanced Microsoft office capabilities and Excel in particular Advanced LinkedIn capabilities. Knowledge of LinkedIn Sales Navigator would be a plus. Excellent oral and written communication and ability to engage, manage, and communicate effectively with stakeholders at all levels of the organization. Strong analytical skills and and proven ability to analyze and interpret internal and external data to generate strategic insights. Attention to detail and accuracy in execution. Self-motivated with the ability to work independently and take initiative Experience with any programming language such as SQL, Python, R Experience with any data visualization tools Salesforce Analytics/ Tableau / Power BI Experience with CRM & Marketing Automation: Salesforce, Pardot or HubSpot, ZoomInfo Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs. We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities. We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.

Brief Position Description: Novotech continues to expand its global commercial capabilities and is seeking a Senior Sales Enablement Analyst for its Bangalore office. This strategic role will support the Business Development team, driving sales lead generation efforts, insights, and analysis to enhance decision-making and contribute to Novotech s continued growth and market leadership. Core responsibilities: Reporting to a Lead Analyst, the Sales Enablement Analyst will: Account-Based Marketing (ABM) Develop and execute personalized marketing strategies targeting high-value accounts. Align marketing efforts with sales teams to enhance engagement and conversion rates. Utilize data-driven insights to optimize account selection and prioritization. Lead Management Identify, nurture, and qualify potential leads to maintain a healthy lead Management Implement lead scoring models to assess prospect readiness and prioritize outreach. Track and analyze lead engagement to refine marketing strategies. Create Dynamic and Static lists for buying Journey and Call to Actioned Marketing Databases Management & Enrichment Maintain and update marketing databases to ensure accurate and actionable data. Conduct data cleansing, enrichment, and segmentation for targeted campaigns. Integrate various data sources (Salesforce, ZoomInfo, Global Data, etc.) for comprehensive insights. Implement the data compliance rule: GDPR Reporting & Analytics Generate detailed reports for Sales Meeting, lead generation, and pipeline health, Executive summary. Provide data-driven recommendations to optimize marketing and sales strategies. Collaborate with stakeholders to present actionable insights from reporting tools. Marketing Insights & Competitive Intelligence Funding Analysis: Track funding trends and investment activities to identify potential opportunities. Pipeline & Milestone Analysis: Monitor key industry projects, product launches, and development phases. Conference Intelligence: Gather insights from industry events, webinars, and networking opportunities. Intent Data Utilization: Leverage behavioral signals to predict buyer intent and target prospects effectively. Mergers & Acquisitions (M&A) Tracking: Assess M&A activities to uncover new business opportunities. Patient Recruitment Challenges: Analyze challenges in clinical trial recruitment and provide strategic solutions. Financial Results Review: Monitor quarterly and annual financial reports for strategic decision-making. Phase Pull-Through: Track drug development phases to anticipate upcoming market needs. Required Qualification(s): Preferred : Degree in Life Science or related field (Pharmacy, Medical, Biology), MBA, Data Science, Business Analytics Acceptable : Undergraduate degree in a business/administrative and information technology related courses of study. Required Professional Experience: 5+ years in sales enablement, business development support, inside sales, or sales operations Required skills: Advanced Microsoft office capabilities and Excel in particular Advanced LinkedIn capabilities. Knowledge of LinkedIn Sales Navigator would be a plus. Excellent oral and written communication and ability to engage, manage, and communicate effectively with stakeholders at all levels of the organization. Strong analytical skills and and proven ability to analyze and interpret internal and external data to generate strategic insights. Attention to detail and accuracy in execution. Self-motivated with the ability to work independently and take initiative Experience with any programming language such as SQL, Python, R Experience with any data visualization tools Salesforce Analytics/ Tableau / Power BI Experience with CRM & Marketing Automation: Salesforce, Pardot or HubSpot, ZoomInfo Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs. We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities. We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.

Position: Medical Coder Ct: HR DEEPA - 7305649640 Job Description: Position: Medical Coder. Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medical reports from doctors, which may include a patients condition, the doctors diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim. Eligibility: All (UG/PG) Life Science& Paramedical Graduates BDS BPT BHMS BAMS Siddha,Unani,Naturopathy {Dip Bsc Msc} Nursing/GNM {B.E M.E} Biomedical Engineering {B.tech,M.tech}Biotechnology Biochemistry Bioinformatics Microbiology Zoology and Advanced zoology Biology Botany Medical Lab Tech Plant biotechnology Pharmacy(B.Pharm M.pharm) Paramedical Physiotherapy Physician assistant Critical Care Technology Medical Biochemistry Medical Record Science Operation Theatre & Anaesthesia Technology {Bsc Msc Dip} Clinical Nutrition Human Genetics Medical Laboratory Technology Medical Sociology Epidemiology Molecular Virology Biostatistics Blood Banking Technology Regenerative Medicine Optom. Genetic Counseling Radiology & Imaging Technology Medical Biochemistry Medical Microbiology Clinical Care Technology Clinical Care Technology Medical Physics {Bsc Msc Dip} Accident & Emergency Care Technology Audiology & speech Language Pathology Cardiac Technology Cardio Pulmonary Perfusion Care Technology Critical Care Technology Dialysis Technology Neuro Electrophysiology Medical Sociology Nuclear Medicine Technology Operation Theatre & Anaesthesia Technology Optometry Physician Assistant Radiology Imaging Technology Radiotherapy Technology Medical Record Science Respiratory Therapy Fitness and Lifestyle Modifications Accident & Emergency Care Technology Critical Care Technology Nursing Aide Operation Theatre & Anaesthesia Technology Ophthalmic Nursing Assistant Medical Record Science Optometry Technology Radiology & Imaging Technology Medical Lab Technology Cardiac Non Invasive Technology Dialysis Technology Dentist Requirement: Knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills Benefits System based job Weekly 5 days duty Day shift with Sat and Sun off Food and Cab provided by company Incentives based on performance Starting salary 12k to 25k with increment in 6 months for experienced. Abroad opportunities available Bonus for referring friends Medical expenses covered by company Provident Fund will be provided Job Location: Chennai, Coimbatore, Vellore, Trichy, Cuddalore, Pondi Salem, Erode, Namakkal, Thanjavur, Nagercoil, Theni,Dindokal Thiruvannamalai, Villupuram, Karur, Tirunelveli,Kanniyakumari Tirupati, Kerala, AP,Tamilnadu,Telangana Reach us : Ct: HR DEEPA 7305649640 Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology GNM DGNM Physician assistant Anesthesia technician Perfusion Technology Medical coder Freshers Medical coding Freshers jobs in chennai Medical coding openings in chennai Wanted Medical coder Freshers jobs Medical coding Medical coder Medical coding Freshers Jobs in chennai Jobs for Passed outs Freshers jobs in chennai Jobs for freshers Nursing jobs for freshers Pharma jobs for Freshers Biotechology Jobs Microbiology jobs Biomedical jobs Bioinformatics jobs Bsc/Msc Jobs Biochemistry jobs Life science jobs in chennai Paramedical jobs in chennai Jobs in Tamilnadu Jobs in Pharmacy Jobs in Hospital GNM STAFF NURSE ANM STAFF NURSE GNM FEMALE STAFF NURSE DGNM FEMALE STAFF NURSE GNM MALE NURSE MALE STAFF NURSE NURSING JOBS IN CHENNAI Perks and Benefits Incentives & Benefits as per Corporate Standards