280 Hematology Jobs - Page 6

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description: Job Title National Sales Head – Public Market, PDT: Location India: About the role : The National Sales Head (NSH) role leads the execution of Takeda’s PDT business unit’s strategy across all channels. The NSH drives sales performance (volume and price) for the Hemophilia business. The role also includes launch of new products within the Business Unit, evaluating/improving sales operational processes and implementing commercial strategies, support contracting and drive sustainable pricing; develop individuals and teams while promoting a winning culture. Sales leader will collaborate with other functional leaders from market access, medical, training, institution business, and marketing to drive the business in a compliant and sustainable way forward. Strategic Planning: Develop and implement comprehensive sales plans to increase market share and achieve sales objectives. Team Leadership: Lead and mentor a diverse team of regional sales managers and sales representatives, fostering a high-performance culture. Performance Monitoring: Track, analyze, and report on sales performance metrics, making data-driven decisions to optimize sales efforts. Customer Relationships: Build and maintain strong relationships with key clients, addressing their needs and ensuring customer satisfaction. Market Analysis: Conduct market research to identify emerging trends, competitive dynamics, and new business opportunities. Sales Training: Provide training and development programs for the sales team to enhance their skills and product knowledge. Collaboration: Work closely with marketing, product development, and other departments to ensure alignment and support for sales initiatives. Budget Management: Oversee the sales department’s budget, ensuring efficient allocation of resources to maximize ROI. How you will contribute : Sales Management: Ensure compliance of the sales organization with all applicable SOPs, India laws and regulations. Establish National sales goals based upon current market trends and aligned to company objectives. Monitor the National sales performance vs. plan and budget. Prepare sales forecasts and update on a monthly, quarterly and annual basis for accurate national sales planning. Work with internal stakeholders to ensure that there is sufficient supply and demand of priority products. Analyze sales data to identify opportunities/gaps across districts, provide recognition and address poor performance in a timely manner. Oversee implementation of promotional activities. Ensure proper allocation and monitoring of budgets. Conduct regular monthly sales reviews, provide coaching, review performance, and build motivation and selling skills of sales personnel. Ensure sales personnel adhere to the code of conduct and conform to the local laws and regulation in their line of work. Ensure SFE parameters are at or above target and continuously improving Business growth: Develop business plan and strategy to increase market share. Provide relevant information from sales activities to marketing teams that can help with crafting productive marketing strategies. Network with potential customers in an effort to promote certain products and to keep abreast with the current developments and trends within the marketplace. Prepare action plans by individuals as well as by team for effective search of sales leads and prospects. Monitor and analyze competitor’s activities and propose counter action. People Development: Inculcate Takeda culture and Takeda values in the team Conduct regular reviews with Business Leads to build more effective communications, understand training and development needs, and provide insights for the improvement of territory’s sales and activity performance. Develop, implement and monitor development program for the team Conduct regular feedback and coaching session and engage them in periodic performance reviews Mentor the sales team and nurture relationships with Business Leads, Business Account Managers in order to help them achieve their goals Collaborate with other stakeholders to ensure effective execution of brand strategies Set performance management objectives based on relevant Sales Force Effectiveness key performance indicators To perform other tasks and duties which may be assigned by immediate supervisor Cross-Functional collaboration: Build and maintain strong relationships with key decision-makers at national, regional, and local levels, including healthcare providers, hospitals, HCPs and government authorities when required Partner with tender and GIB (Government Institution Business) teams to service government accounts and make Takeda products available to patients Partner with the market access team to develop and execute strategies to continuously increase access for patients Partner with training and development team for development and implementation of an effective sales and in-clinic effectiveness trainings Work closely with distribution management team to ensure high quality distribution network through India and tech lead order management system What you bring to Takeda : Minimum Graduate/ Post Graduate. MBA will be an added advantage. At least 15 years of pharma/biotech, healthcare experience required with last 2-3 years in managing national sales. Candidate with sales experience in Hematology specialty and public market will be added advantage. People leadership experience a must Excellent communication skills, the ability to engage and motivate a diverse group of sales professionals Ability to work in a matrix sales organization. Ability to serve as a role model for the organization Strong interpersonal skills Strong channel management experience (distributors, aggregators etc.) a must Able to operate in a fast-paced and changing market environment. Ability to manage, optimize and identify opportunities with process enhancement and program growth Skilled at providing market recommendations and customer feedback to the leadership team Knowledge of CRM software and Microsoft Office Suite. An ability to understand and analyze sales performance metrics. Behavioral Competencies and Skills : High-impact communication/presentation Skills Stakeholder management Credible/authentic presence and leadership skills Ability to build network within govt. machinery/establishments as well as private institution. Integrity, honesty, perseverance, fairness People Manager, Team player and capability to foster an inclusive environment within the team and beyond. Other Information: Travelling requirement : Ability to travel 70% of the times, including ability to travel overnight and occasionally on weekend More about us : At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Empowering our people to shine : Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations: Mumbai, India Worker Type: Employee Worker Sub-Type: Regular Time Type: Full time Show more Show less

Consultant Pathologist Managing Hematology and Clinical Pathology department with respect to quality reporting of samples; manpower, material and equipment management and create a healthy environment for quality of service to be delivered. Reviewing slides and reports in Hematology and Clinical Pathology sections. Review of reports for Biochemistry, Immunoassays and Serology sections in coordination with Biochemist and Microbiologists respectively Ensuring turnaround time of laboratory tests Conducting training sessions/ seminars for staff Monitoring compliance of staff with the laboratory safety norms Query resolution on test reports and interaction with clinicians. Monitoring actual consumption of stocks versus the number of tests performed. To oversee equipment maintenance and new instrument installation. Review effective and rational utilization of kits and equipment Review of all internal & external Quality assurance data as per labs quality management system, in order to ensure quality reporting of tests performed. Review of IQAP and EQAS. Reviewing Validation/ Verification data of kits prior to utilization at the laboratory bench Presenting the departments for Audits as and when necessary Instituting timely corrective actions for sub-optimal proficiency test results as well as any non-conformances raised during the audits

Age Limit: 30 years maximum, as on the last date for application Education: MSc Botany / Zoology / Physiology / Biochemistry / Biotechnology with minimum 1year project assistant experience. Required skills: Cell Isolation & culture in Vivo and in Vitro Toxicity Histology, Immunocytochemistry, Spectrophotometry Analysis, Isolation & Characterisation of Proteins & Biomolecules (Chromatography), Native SDS & Gradient Gel Electrophoresis, Western Blotting, Northern Blot PCR, Real Time PCR, Microscopy, Fluorescence Microscopy, Immunofluorescence Cloning, Characterisation & functional analysis of gene. Responsibilities: Contribute to planning and setting up of the Scientific Support Services at RISE Foundation. Participate in specification, purchase and installation of instruments/ equipment. Operate lab in coordination with scientific mentors and advisors of the Rise Foundation (including IISER scientists) Support incubatees and budding entrepreneurs by offering Scientific Support services. Arranging training programs and other events related to Scientific Support Services keeping records/SOPs/LOG BOOKS of the equipment uses of innovators/ incubatees related with incubation centre work and periodic calibrations of the equipment of the incubation centre. Keeping the documents of maintenance contracts, warranties of the equipment periodic assessment of the necessity of maintenance work, estimation of cost of maintenance and initiating the process for execution of the maintenance works. Coordination with the laboratories (IISER and others) for utilization of their facilities to support the incubatees Prior assessment of the requirements of consumables in the incubation centre and informing the Purchase Manager. Assisting, if any external personnel visit the incubation centre for inspection. Contribute to building scientific support systems and resources for RISE Foundation incubatees including specific expertise and library. Contribute to defining, raising money and running projects as they come up Other tasks as requested from time to time by the COO.

RolePath Lab Technician Type Full Time Job description : - Receive, label and analyze samples (blood, toxic, tissue etc.) - Design and execute laboratory testing according standard procedures, make observations and interpret findings. - Conduct experiments under defined conditions to verify/reject various types of hypotheses using refined scientific methods. - Organize and store all chemicals substances, fluids and compressed gases according to safety instructions. - Record all data and results in specified forms (paper and electronic) with accuracy and responsibility. - Maintain equipment and assist in ordering laboratory supplies. - Ensure that all safety guidelines are followed strictly at all times and maintain a clean and orderly environment. - Medical Record keeping. - Day to Day operations. - Analyze reports. This job opening was posted long time back. It may not be active. Nor was it removed by the recruiter. Please use your discretion.

Role Biochemist Type Full Time Job description : - Carry Out Detailed Experimentation Projects Both Basic and Applied Upon the Direction of the Biochemistry Manager - Exercise Knowledge and Experience in Regulatory Agency Rules and Inspection Protocol as Well as Clinical Chemistry Best Practices to Enable the Most Advanced Research Capabilities Possible in the Laboratory - Isolate, Analyze and Conduct Diverse Experiments with Proteins, Dna and other Types of Molecules, and Research the Effects of Different Treatment Protocols On the Health of Cells and Larger Biological Functions - Write Technical Experimentation Reports to Clearly Describe the Method Used to Research and the Results Obtained and Conduct Extensive Data - Analyses On the Results to Ensure the Highest Degree of Accuracy - Conduct Presentations with Hospital Staff Regarding Research Results and Analysis - Continually Strive to Learn New Information in the Biochemical Field By Attending Educational Opportunities, such as Medical Conferences - Act as a Hospital Resource to Consult with Clinical Staff Regarding Recommended Test Orders as Well as Their Results This job opening was posted long time back. It may not be active. Nor was it removed by the recruiter. Please use your discretion.

A Microbiology Tutor provides academic support to students by explaining key concepts in microbiology, including bacteria, viruses, fungi, and immunology. - Teaching to paramedical courses - making notes etc...

1) Slide assessment will be done in Delhi for histopath role for Meerut-in respective city and virtual interview for Shimla 2) Notice period buyout option available 3) No accommodation 4) Immediate joining (max 10 days) Pls whatsapp at 9682185990 Required Candidate profile Freshers who have done histopathology in residency or want to learn histopathology can also apply

Job Description Role responsibilities -Consultant Transfusion Medicine Blood Bank Management:Overseeing all aspects of blood bank operations, including blood donor screening, blood component preparation, storage, and distribution. Compatibility Testing and Evaluation:Conducting blood typing, compatibility testing, and other specialized immune-hematology tests to ensure safe blood transfusions. Clinical Liaison and Consultation:Consulting with clinical teams on blood requirements, transfusion reactions, and best practices, including managing BMT and hemo-oncology patients. Quality Assurance and Improvement:Participating in EQAS (External Quality Assessment Schemes), audits, and other activities to ensure the highest quality of transfusion services. Policy Development:Drafting and implementing policies, procedures, and guidelines for safe and effective transfusion practices. Education and Training:Providing education and training to healthcare professionals on transfusion medicine principles and practices. Research and Development:Contributing to research initiatives in the field of transfusion medicine. Clinical Responsibilities:Evaluating patients for BMT and hemo-oncology, coordinating stem cell harvest, granulocytapheresis, and other specialized procedures. Management Responsibilities:Drafting SOPs (Standard Operating Procedures), policy documents, and ensuring compliance with regulations like Drug control License and NABH, according to one example. Academic Responsibilities:Participating in departmental teaching activities and allied specialty meetings. Qualifications: MBBS, MD, DML in Transfusion Medicine. Registration with relevant medical bodies, such as the General Medical Council (GMC). Experience in blood banking and transfusion medicine. Strong clinical skills and knowledge of immunohematology. Excellent communication and interpersonal skills. Ability to work independently and as part of a team Preferred candidate profile As per Market standard. Specialisation Transfusion Medicine APPLY FOR THIS JOB Upload Resume Note:(Only pdf and docx files are allowed) I authorize Dr.Kamakshi Memorial Hospital Pvt Ltd.HR Persons to call me *. Other jobs you may like Designation: Consultant-Geriatrician Location: Pallikaranai Experience: 5 - 10Years Full Time Full Time Designation: Consultant General Medicine

Company Description Sahyadri Hospitals operates a network of 11 hospitals with over 1200 beds and is supported by more than 2500 clinicians and 3000+ supporting staff. The organization specializes in various medical fields including neurosciences, hematology, oncology, cardiology, orthopedics, liver transplant, and more. With a significant presence in Pune and Nashik, Sahyadri Hospitals is committed to touching millions of lives through premier healthcare services. Role Description This is a full-time on-site role for a Deputy General Manager located in Pune. The Deputy General Manager will be responsible for overseeing day-to-day hospital operations, ensuring regulatory compliance, managing staff and resources, and implementing strategic initiatives to improve patient care and operational efficiency. The role also involves budgeting, supervising administrative functions, and liaising with clinical departments to facilitate smooth organizational flow. Qualifications Management skills in healthcare administration, operations, and leadership Financial acumen and budgeting skills Strong communication and interpersonal skills Ability to implement strategic initiatives and improve operational efficiency Regulatory knowledge and experience in compliance Bachelor's or Master's degree in Healthcare Management, Business Administration, or related field Experience in a hospital or healthcare setting is a plus Proven track record of effective team management and leadership Show more Show less

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description Job Summary We are looking for experienced and dynamic Team Lead in Medical Affair team for Hematology TA to actively contribute to the organization/business by taking people managerial responsibility and being responsible for the scientific, technical and ethical soundness of all policies, statements and endeavours. He/she will need to provide high quality and timely service in the areas of product commercialization/promotional support, interactions with healthcare professionals, continuing medical education, clinical research, sales force training, medical information, and performance/people management, and business support in the areas of new product development, regulatory affairs, quality standards, and information technology; alliance management may be included as applicable. Roles & Responsibilities You will be responsible to provide tactical and strategic inputs, and business/technical expertise, to Product Management towards ethical promotion of assigned products, in the operational areas listed You will be responsible for providing strategic inputs for marketing and brand plans, overseeing the design and execution of medical-marketing programs, and facilitating interactions with healthcare professionals. Additionally, you will initiate, review, and approve promotional and educational materials while ensuring compliance with relevant SOPs, regulations, and industry codes. You will be responsible for developing, reviewing, and approving protocol documents and supporting materials for various clinical projects. Additionally, you will collaborate with Global Medical Affairs and Clinical Development, organize training sessions for project teams, and provide medical support for safety reporting and ongoing local studies. Furthermore, you will contribute to the planning and execution of Investigational New Drug Applications (NDAs). You will be responsible to provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external customers. You will be responsible for training the Sales Force on basic sciences/assigned products and pre-launch and launch training for new products. You will assist the New Product Planning team in preparing business cases and pre-commercialization programs for global products, development of local formulations and line extensions. Additionally, you will provide support in market research, stakeholder mapping, and early access programs. You will also collaborate with various departments to evaluate commercial opportunities, including licensing, acquisitions, and co-promotion. You will be responsible for providing medical and product expertise in the registration of new products/indications, as well as defending marketed products to various stakeholders. You will also oversee the writing and review of labelling documents and provide medical support for the processing of adverse event reports, adhering to relevant SOPs and practices. You will be responsible to develop and share expertise in identified medical and/or scientific therapeutic area, including but not limited to disease areas, markets, products (DRL products and key competitors) and services. You will be responsible to develop and share expertise in a specific medical/scientific subject, including protocol design, development, and training, Pharma co economics, Outcomes Research, Health Technology Assessment, New Product Evaluation, Disease Management Programs, Intellectual Property Protection and Patents, and Medical Information You will be one-point Medical Affairs contact for Customer Relationship Management and operational liaison in the various functional domain. You will be responsible for fostering a culture of learning and development and managing the Medical Affairs staff, providing training, guidance, and support across various functional domains, ensuring adherence to company values and behaviours, and. You will be responsible to support cluster Head Medical Affairs in budgeting, provisioning and expense control. Qualifications Educational Qualification- Post-graduate degree in Pharmacology or other Medical speciality/ Graduate degree in Medicine Minimum work experience - 6-12 years of relevant experience as Medical Advisor with a minimum of 3 years of experience in Hematology TA. Must have a prior experience of NCE/NBE launches in Hematology TA Skills & attributes – Technical Skills Basic knowledge of pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines Knowledge of “pharmaceutical medicine” including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics and relevant Therapeutic Area/Products Expertise in clinical trial design and methodology, and understanding of interfaces, and conduct Behavioural Skills Communication skills, both written and verbal (including medical writing and presentation skills) Analytical skills and reasoning, and sound medical judgment/decision making Interpersonal skills, internal & external networking and the ability to impact and influence. Additional Information About the Department Global Generics India Global Generics India business journey began in 1986. In the last three decades, we have grown as a trusted name in the healthcare industry and rank as one of the top 10 Pharma Companies in the Indian Pharma Market (IPM) as per IQVIA MAT (November 2022). Our commitment to Lead Ahead has helped us move ranks from 16th position to 10th position (IPM) in the last four years. We are a fast-growing organisation with double-digit growth and significant market share in domestic markets. Currently, we rank among the top 5 in oncology, anti-allergy and gastrointestinal diseases and the top 10 in a few other therapy areas. Our focus is on leveraging our digital capabilities, collaborations, innovations and inorganic opportunities to become the top 5 companies in the Indian Pharma Market. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/ Show more Show less

The Associate Medical Expert in TCO (Translational Clinical Oncology), is the medical leader for assigned global, roll-over and long-term follow-up studies, and studies in the close-out phase. They may also provide medical support for assigned aspects of a global, active, TCO study, under the leadership of a Clinical Program Leader (CPL) and / or Medical Expert TCO (Translational Clinical Oncology) is a department under Biomedical Research division, and is responsible for designing and executing out early phase (first in human) clinical studies in patients with cancer. It acts as a bridge between drug discovery and late phase clinical development and strives to deliver transformative new medicines for oncology conditions. About the Role Major accountabilities: Provides medical support to Clinical Program Leader (CPL) and / or Medical Expert. Medical support may include, but is not limited to, contributing to clinical sections of protocols and/or amendments, Informed Consents, publications, regulatory documents such as Investigator Brochures, responses to Health Authority questions and conducting ongoing review of clinical trial data, with oversight of TCO deliverables. May act as the medical monitor to support overall program safety reporting (eg, Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety Team. Contributes to clinical/scientific elements of TCO - related submission documents, including preparation and review of project documentation for Health Authority submission, including briefing books, IBs, Annual Safety Reports, responses to Health Authority questions etc Contributes to the ongoing clinical trial data medical/scientific review across assigned TCO studies and coordinates data analysis and interpretation Supports conduct of dose escalation meetings, investigator teleconferences and site initiation visits etc Accountable for assigned close-out, roll-over and long-term follow-up studies, ensuring Clinical Study Report review, consistency and quality of clinical study reports (CSR) in collaboration with CSR medical writing team, and publication of studies across assigned TCO projects - either directly as lead author or by providing leadership to the medical writing team Maintains expert knowledge of ICH-GCP, external regulations and procedures, and supplements by training and practice of Novartis SOPs and internal policies. Advocate continuous improvement of quality Key performance indicators: Evidence of high-quality medical input to assigned studies to ensure execution according to timelines and ensuring adherence to international and local regulations. Evidence of quality medical and scientific review of clinical trial data Demonstrates excellent scientific writing skills to enable the development of high-quality documents including but not limited to clinical trial protocols, trial reporting (eg CSR), and regulatory documents (eg IB, DSUR). Contribution towards objectives set for the department. Feedback from external and internal stakeholders. Clearly demonstrates Novartis Values and Behaviors. Minimum Requirements: MD or equivalent medical degree required. Advanced knowledge and clinical training in a medical/scientific area (eg, internal medicine / pharmacology etc) with medical council certification required. Experience in hematology / oncology preferred. Work Experience: At least 2 years of pharmaceutical/biotech industry experience or at least 4 years of clinical practice experience in the hospital setting Knowledge of Good Clinical Practice (GCP). Strong operational project experience including excellent planning, prioritization, problem solving and organizational skills. Used to managing multiple priorities. Demonstrated operational excellence and scientific contribution to clinical or preclinical projects. Clear written and verbal expression of ideas, an active/proactive communicator. we'll-developed interpersonal skills, with a proven record of accomplishment of successfully interacting with, influencing and building strong positive relationships. Used to working independently and in a team, being flexible and adapting in a changing environment. Skills: Clinical Monitoring. Clinical Research. Clinical Trial Protocol. Clinical Trials. Decision Making Skills. Drug Development. Health Sciences. Lifesciences. Regulatory Compliance. Languages : English.

Preparing and administering radiopharmaceuticals orally or by injection or inhalation. Explaining the imaging procedure to patients, answering questions, and ensuring their comfort while placing them in the appropriate position for scanning. Operating imaging equipment, such as PET and SPECT scans. Processing images on the brain, thyroid, bone, heart, lungs, kidneys, and liver on the computer. Monitoring patients for unusual reactions to radioactive drugs. Keeping detailed records of the amount and type of radiopharmaceutical used and of the procedure. Producing computer-generated or film images for interpretation by the physicians. Following safety procedures to protect staff and patients from unnecessary radiation exposure. Maintaining and examining medical machines and imaging equipment. Monitor the patient to check for unusual reactions to the drugs Keep detailed records of procedures Maintaining current knowledge of the frequent advances, innovations, and developments in the field.

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. PSI’s business is about conducting clinical research of novel medications. We work at the interface of R&D, pharmaceutical industry and healthcare science and provide services to big and mid-sized pharmaceutical companies. We help our clients to generate data about safety and efficacy of medications and bring the best ones to market. By conducting global clinical research trials, PSI makes cutting-edge treatment available in drugstores all over the world and helps patients with serious medical conditions to improve or even save their life. Help us to make sure that PSI medical and business documents are clear to patients, physicians, regulatory authorities, and clients. We offer an inspiring story of the company that has grown organically from a handful of countries to global presence. PSI is a mature company with standards and practices, but we do not stand still. Every day, there is a figurative Everest to climb, and you will not get bored here. Job Description PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being. Responsibilities: Advise clients, project teams, sites, data safety monitoring boards, regulatory agencies and third-party vendors on medical matters Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations Review and analysis of clinical data to ensure the safety of study participants in clinical studies Ensure that the reported data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments Address safety issues across the study from sites and the study team Review listings for coded events to verify Medical Dictionary for Regulatory activities Participate in bid defense meetings Assist in Pharmacovigilance activities Identify Program risks, and create and implement mitigation strategies with Clinical Operations Ability to organise and lead clinical development advisory boards and safety monitoring boards Ensure Study team compliance with local regulatory agencies, ICH and GCP guidelines Review and sign off clinical documents with respect to medical relevance As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them. Qualifications Medical Doctor (MD) degree with Board Certification/Specialization in (Oncology, Gastroenterology, Infectious Disease or Onco-Hematology) is an essential requirement. Familiar and comfortable with clinical concepts, practices and local regulations regarding clinical research trials experience with local health authority interactions leading to drug approval strongly preferred. Ability to interact with and train clinical monitors and physician investigators, and build constructive, trusting and respectful relationships with colleagues at all levels within and outside the organisation. Must possess excellent leadership, communication, presentation, and organisational skills and be able to exercise sound critical thinking and problem-solving skills and execute position responsibilities with minimal guidance. Proficiency with MS Office applications. Additional Information Join our highly dedicated team of clinical research professionals with +250 Medical Doctors onboard, and make a tangible difference within a professional and energetic organization founded by scientists. Show more Show less

Diagnose diseases by studying body tissues, fluids, and cells. To analyze samples, perform laboratory tests, and provide reports to assist in disease diagnosis and treatment. Regular training and managing the department.

Summary The Medical Expert in TCO (Translational Clinical Oncology) is the medical leader for assigned global, roll-over and long-term follow-up studies, and studies in the close-out phase. They may also provide medical co-leadership for assigned aspects of one or more global, active, TCO study, under the leadership of a Clinical Program Leader (CPL) TCO (Translational Clinical Oncology) is a department under Biomedical Research division, and is responsible for designing and executing out early phase (first in human) clinical studies in patients with cancer. It acts as a bridge between drug discovery and late phase clinical development and strives to deliver transformative new medicines for oncology conditions. About The Role Major accountabilities: Provides medical support to Clinical Program Leader (CPL) leading the program. Medical support may include, but is not limited to, contributing to clinical sections of protocols and/or amendments, Informed Consents, publications, regulatory documents such as Investigator Brochures, responses to Health Authority questions and conducting ongoing review of clinical trial data, with oversight of TCO deliverables. May act as the medical monitor to support overall program safety reporting (e.g., Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety Team. May represents CPL at project team meetings (e.g. CTT) and may provide inputs to project strategy May represent CPL at Investigator teleconferences including dose escalation meetings and site initiation visits. Oversees the clinical/scientific elements of TCO – related submission documents, including preparation and review of project documentation for Health Authority submission, including briefing books, IBs, Annual Safety Reports, responses to Health Authority questions etc. Leads the ongoing clinical trial data medical/scientific review across assigned TCO studies and coordinates data analysis and interpretation Accountable for assigned close-out, roll-over and long-term follow-up studies, ensuring Clinical Study Report review, consistency and quality of clinical study reports (CSR) in collaboration with CSR medical writing team, and publication of studies across assigned TCO projects - either directly as lead author or by providing leadership to the medical writing team Manages stakeholder engagements internally and externally Mentors and coaches junior TCO team members in India Maintains expert knowledge of ICH-GCP, external regulations and procedures, and supplements by training and practice of Novartis SOPs and internal policies. Leads or assists with relevant trainings across TCO India Advocate continuous improvement of quality Ensure all activities of associates comply with company standards and local regulations Key Performance Indicators Management of assigned studies to ensure execution according to timelines, and with high quality, ensuring adherence to international and local regulations. Demonstrates excellent scientific writing skills to enable the development of quality trial reporting, and regulatory documents. Strong evidence of quality medical review of trial data and quality contributions to clinical sections of e.g. protocols, IBs, DSURs and CSRs Contribution towards objectives set for the department. Feedback from external and internal stakeholders. Clearly demonstrates Novartis Values and Behaviors. Minimum Requirements Education: MD or equivalent medical degree required. Advanced knowledge and clinical training in a medical/scientific area (e.g., internal medicine / pharmacology etc.) with medical council certification required. Experience in hematology / oncology preferred Work Experience At least 5 years of pharmaceutical/biotech industry experience At least 2 years of clinical practice experience in the hospital setting. Experience with oncology clinical trials Experience with early development clinical trials Knowledge of Good Clinical Practice (GCP). Strong operational project experience including excellent planning, prioritization, problem solving and organizational skills. Used to managing multiple priorities. Demonstrated operational excellence and scientific contribution to both clinical and preclinical projects. Strategic thinking: ability to network with and influence key stakeholders, clear and logical presentation of complex strategic issues. Clear written and verbal expression of ideas, an active/proactive communicator. Well-developed interpersonal skills, with a proven record of accomplishment of successfully interacting with, influencing and building strong positive relationships. Used to working independently and in a team, being flexible and adapting in a changing environment. Skills Clinical Monitoring. Clinical Research. Clinical Trial Protocol. Clinical Trials. Decision Making Skills. Drug Development. Health Sciences. Lifesciences. Medical Strategy. Regulatory Compliance. Languages English. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Show more Show less

About Bristol Myers Squibb: At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology, and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Key Responsibilities Functional and Technical: QA Review and approval of validation deliverables associated with various BMS enterprise systems including but not limited to clinical study databases electronic Case Report Forms (eCRF), enterprise commercial manufacturing systems such as electronic laboratory notebooks and manufacturing execution systems, and various VEEVA Vault based configurations. Ensure adequate and timely quality assurance / regulatory compliance support Provide support during regulatory agency and third party inspections Research new technologies, understand existing processes, and reference recognized standards and frameworks Pursue continuous professional development through company paid internal/external training, certifications and/or continuing education. Identify opportunities for continuous improvement Adherence to BMS Core Behaviors Conduct risk & impact assessment to determine the extent of validation and qualification and ensure right sized validation effort for programs Demonstrate critical thinking around interpreting business and industry challenges and recommending best practices-based solutions to improve products, processes, systems Implement organizational IT controls in accordance with applicable regulations and the ability to evaluate and understand the impact of new regulations and requirements Review Periodic Review assignments completions for applications in a timely manner Support responses to application CAPAs and Audits as they relate to health authority investigations and internal audits in a timely manner-in coordination with multiple stakeholder teams Qualifications & Experience: B.E./B.Tech. or equivalent in computer science, engineering, life science field A minimum of 5-7 years of experience in Quality Assurance, IT Compliance and computer systems validation (CSV) in the pharmaceutical industry, including at least 3 years of managing/overseeing IT Compliance and CSV projects Candidate must have a strong understanding of 21 CFR Part 11, EU Annex 11, Data Integrity principles, GAMP and Agile methodologies. Additionally, good understanding of Computer Software Assurance principles desired. Understanding of quality risk-management concepts (ICH Q9) preferred Proven experience in the interpretation and understanding of GxPs for the controlled management of electronic records and signatures Previous experience as a computer system validation / quality assurance / quality control analyst for a life sciences company regulated by the FDA (or equivalent) preferred Familiarity with the drug development process from discovery through to regulatory filing and approval of drug applications as well as commercial manufacturing processes Experience with driving validation strategies across across the end-to-end product lifecycle as well as experience with widely used IT Enterprise platforms (SAP, Veeva, ServiceNOW etc.) General knowledge of IT applications, IT infrastructure, architecture of computer systems including SaaS, IaaS as well as networks, operating systems, databases, and software tools Candidate must have strong knowledge of IT testing practices and methodologies in the pharmaceutical GxP space-and good working knowledge of tools like ALM and Valgensis Ability to make decisions that impact own work and other groups/teams and works with minimal supervision Ability to support various projects, create and work within internal timeliness, solve problems, deliver on commitments and utilize interpersonal skills in a cross-functional team Demonstrates openness to learning and developing. Takes a responsibility for their own and team’s development and growth Demonstrates an understanding of factors driving team performance and how they contribute to?the team's overall success Strong sense of ethics, diplomacy and discretion Commitment to Quality Fluent in English, with proven professional working proficiency in English for reading, writing and speaking. including the ability to deliver clear and articulate presentations Show more Show less

Company Description HEMATO-ONCOLOGY CLINIC (AHMEDABAD) PRIVATE LIMITED is a hospital & healthcare company located near Samved Hospital in Ahmedabad, Gujarat, India. Role Description This is a full-time on-site role for a Medical Transcriptionist at HEMATO-ONCOLOGY CLINIC (AHMEDABAD) PRIVATE LIMITED. The Medical Transcriptionist will be responsible for transcribing medical documents, utilizing medical terminology, and typing documents accurately. Qualifications Transcribing and Transcription skills Medical Terminology knowledge Typing proficiency Experience in providing Transcription Services Attention to detail and accuracy Ability to work effectively in a fast-paced healthcare environment Knowledge of hematology and oncology terminology is a plus Associate's degree in Medical Transcription or related field Job Types: Full-time, Permanent Pay: Up to ₹30,000.00 per month Benefits: Health insurance Leave encashment Paid sick time Paid time off Provident Fund Schedule: Day shift Morning shift Application Question(s): The salary range is up to 30k. Please apply only if you are comfortable with this salary. Experience: Medical transcription: 4 years (Required) Location: Thaltej, Ahmedabad, Gujarat (Required) Work Location: In person

The candidate will be responsible for installation, preventative maintenance and breakdown repair of IVD analyzers (Clinical Chemistry/CLIA/Hematology/Others). Required Candidate profile Candidate must have previous experience handling Hematology and Biochemistry analyzers.

Job Description Wondering whats within Beckman Coulter Diagnostics? Take a closer look. At first glance, youll see that for more than 80 years weve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. Were building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and youll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, were working at the pace of change to improve patient lives with diagnostic tools that address the worlds biggest health challenges. The Territory Customer Support Engineer - Jodhpur for Beckman Coulter Diagnostics is responsible for installing and maintaining instruments and systems in a laboratory environment, delivers basic operational training at installation, and provides effective product and customer support. Ensures Preventive Maintenance planning (PM) & Modification (MODs) planning are performed in a timely manner, seeks timely support for difficult product issues avoiding unnecessary downtime, performs timely reporting of his activities, maintains excellent customer relationships, specifically with his/her directly assigned accounts. Adheres to field service policies, procedures, and standards, maintains recommended spare parts for his product range, ensures appropriate spare parts stock, and travels within the territory. Available to travel on short notice. This position is part of the Service Team-North India located in Jodhpur and will be Fully Remote. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Service Team-North India and will report to the State Service Manager responsible for managing service professionals handling the area of Rajasthan. If you thrive in a challenging, passionate, instrumental, and competitive role and want to work to build a world-class service provider and healthcare organizationread on. In This Role, You Will Have The Opportunity To Grow along with a leading IVD segment organization Provide on-site support for our instruments which will lead to advancing healthcare and patient support, and provide immediate support to achieve client delight. Ability to interact with our team of service professionals and other cross functions which are very critical for the role. The Essential Requirements Of The Job Include Diploma or Graduation - Electrical/Electronics/Biomedical Engineering (Any subjects with electrical and electronics in the curriculum) Three years of any type of basic experience on In-Vitro Diagnostics Equipment (Hematology, Chemistry, or Immunoassay), Should have knowledge of Networking and Interface related issues, also good in MS-Office, Teams, Networking. Can logically resolve or troubleshoot in times of crisis and leverage expert help. It would be a plus if you also possess previous experience in: Can independently handle 1 or more product groups (example Immunoassay Analyzer, Hematology Analyzer or Chemistry Analyzer) with timely expert support. Able to identify application vs. service issues and collaborates to resolve. Ability to prioritize customer needs. Ability to coordinate and collaborate with other functions to achieve client delight. At Beckman Coulter Diagnostics we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide. Join our winning team today. Together, well accelerate the real-life impact of tomorrows science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace, and throughout the markets we serve. Our associates, customers, and shareholders contribute unique and different perspectives as a result of these diverse attributes. Show more Show less

Position - Area Sales Manager - Diagnostic Sales (Delhi & Bangalore ) Experience- Min 4yrs Age - 40 Max Location- Delhi/ Bangalore Ideal Candidate would be someone who has experience in selling any IVD invitro diagnostic instruments and reagents Plz note experience in selling invitro diagnostics instruments and reagent is mandatory Interested candidates can share their updated profile on hiring@apexservices.in

Avience Biomedicals is looking for SALE & SERVICE ENGINEER to join our dynamic team and embark on a rewarding career journey Technical Support: Respond to service inquiries, troubleshoot technical issues, and provide solutions Maintenance and Repair: Perform routine maintenance, inspections, and repairs on systems or equipment Installation and Setup: Install, configure, and set up new systems or machinery as required Testing and Diagnosis: Conduct tests, analysis, and diagnostic procedures to identify problems and recommend solutions Customer Interaction: Interact with customers, clients, or internal stakeholders to understand their needs and address concerns Documentation: Maintain accurate records of service activities, reports, and documentation Training and Guidance: Provide training and guidance to users or clients on the proper use and maintenance of equipment or systems Required Skills and Qualifications:Technical Knowledge: Proficiency in relevant technologies, systems, or machinery Problem-Solving Skills: Ability to diagnose and resolve technical issues efficiently Communication Skills: Strong verbal and written communication for interacting with clients and documenting procedures

Specialists Hospital is looking for Senior Lab Technician to join our dynamic team and embark on a rewarding career journey Assist with testing and calibrating lab equipment in preparation for specific tasks Analyze retrieved data and prepare reports for laboratory management Experience in data collection and interpretation as well as the storage and retrieval of samples in a laboratory setting

Experience in school setup is mandatory To assist students and teachers in conducting practical and experiments maintenance and proper arrangements of all equipment s and apparatus in the lab

Position- Pathology Technician Experience- 1-15 years Qualification- BMLT + DMLT (Mandatory) Location- Jamshedpur Skills- Biochemistry/ Hematology/ Immuno- Analyzers / Routine Clinical Pathology / Microbiology Share your CV- 8457045949

We are looking for a Part time Pathologist for Pune ( Kothrud area) Working Hours: 2 hours per day , 8:30 AM to 10:30 AM. must have atleast 1 year experience post MD/ DCP/DNB Remuneration - 3 lacs pa share CV at hr@oncquest.net