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    (Last Updated: Mar 29, 2024)
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MBBS Fresher

Botmatrix Services Private Limited

Full time
  • 0-1 years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 19, 2024
  • End Date: May 19, 2024
  • 0-1 years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 19, 2024
  • End Date: May 19, 2024

One of our clients, a well established hospital with branches in Bangalore, Mysuru, Mumbai and Delhi is looking for Fresher MBBS Doctor Qualifications and Experience Experience: Fresher Education: MBBS   Responsiblities Conduct regular thorough examinations on patients to check and record their health and normal physical development Examine sick patients to determine their condition and ask intuitive questions to gather information about symptoms Reach an informed diagnosis based on scientific knowledge and individual medical history Prescribe medications and give detailed instructions for administration Prescribe and interpret appropriate lab tests to gain more information about possible infections or abnormalities Prepare and administer vaccines according to the governmental vaccination plan Examine and treat injuries and refer the patients to physicians of other disciplines when necessary (e.g. surgeons, ophthalmologists, orthopedists etc.) Advise patients on diet, exercise and disease preventive measures Keep updated records of patients illnesses, surgeries or other medical episodes allergic shocks, injuries etc.

  • mbbs
Premium

Neonatologist/Pediatric Intensivist

Cloudphysician Healthcare

Full time
  • 4+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 12, 2024
  • End Date: May 12, 2024
  • 4+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 12, 2024
  • End Date: May 12, 2024

Responsibilities Caring for neonates at the remote NICUs from a centralized care center  Manage these patients and document their progress, troubleshoot ICU issues, coordinate bedside team in accordance with global standards, and escalate issues Should be aware of ICU patients monitoring parameters like SpO2, cardiorespiratory, NIBP, Invasive BP, CVP, ventilation parameters, non-invasive ventilation parameters, CPAP/HFNC settings and others Conducting tele rounds which involve patient review, daily rounds, review of labs and radiology, drug charts, compliance to protocols Liaising with the bedside team actively and providing critical care expertise in real time to augment the delivery of critical care to the NICUs Check-ins with regular intermittent tele rounds on sick patients and initiating appropriate actions with the help of the tele NICU team in collaboration with the bedside team Documenting patient-level data and communication in our smartICU platform, RADAR keeping records of their health in NICU, diagnosis and documenting patients' symptoms and medical history. Identifying changes in the infant?s symptoms and intervening in emergency situations Following appropriate guidelines and schedules Keeping and tracking records for vital signs like temperature, pulse, breathing, oxygenation and blood pressure, as well as any signs of distress due to birth asphyxia and trauma, respiratory distress, apnea, aspiration, sepsis, etc., in critically ill infants.   Qualification & Experience Fellowship in Neonatology or Pediatrics hands-on NICU experience in a well-reputed hospital  4 to 6 years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

  • Operations
  • Inspection
  • Management
Premium

US Medical Omnichannel Lead-Associate Director

Eli Lilly and Company

Full time
  • 10+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 10+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities Direct the delivery team to take ownership and deliver best possible outcomes through a sound data management, analytics and operations mindset. Work closely with stakeholders to ensure expansion and penetration of Omni use-cases with medical teams. Create a framework for communication, project management and execution across BUs to help drive best practices Take ownership of design, development, maintenance and operations Be a mentor for team members, and drive upskilling plans for LCCI team Serve as trusted career advisor, and work with functional leadership and HR to identify career opportunities for these team members, both systemically (career path development) and with individuals as needed Develop a pipeline of right talent and leadership, and contribute to an inclusive community of analytics expert practitioners Drive standardization, automation agenda across business units to help scale the delivery operations     Qualification & Experience Master’s degree in management/ pharmaceutical or a related field from a premium college Bachelor’s Degree with 12+ years of relevant experience in an allied fucntions such as: BI, data analytics, Omnichannel, integrated marketing, supporting Pharma/Lifesciences Commercial or Medical ops internally or in consulting; at least 6+ in leading teams  

  • pharma
  • Quality control
  • Management

Associate Medical Advisor

Eli Lilly and Company

Full time
  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities Product or Molecule Safety Physician / Lead Physician Provide global medical leadership and input into all aspects of safety of assigned product(s) including surveillance programs and risk management planning. Ensure proactive safety surveillance: lead risk management activities for assigned products globally lead and guide the surveillance activities of scientists on the team including signal detection and clarification activities and risk evaluation activities; provide support, training and continued improvement as appropriate manage decisions and actions to be taken, including communication to appropriate customers (e.g., Product Teams, Management, Affiliates and Regulators) and liaise with GPS Medical Area Directors and with Lilly Medical Therapeutic Area Team Leaders and Directors, as appropriate, to fulfill safety obligations; Supervise and review reports on safety issues and their implications for the Core Safety Information and Core Risk Minimization Activities, represent PV position to Global Patient Labeling Committee and/or the Safety Review Committee as appropriate. Build collaborative working relationships with other Global Patient Safety Physicians and development and brand teams medical globally to ensure full cooperation and high quality medical evaluation of safety data for global regulatory purposes. Represent GPS Medical and/or Product on appropriate committees/product development and brand teams. Provide medical support for Global Patient Safety activities and reports within the department, as appropriate. Provide Global Patient Safety expertise to internal customers (e.g., regulatory, early phase development, business units). Provide medical input for review of Adverse Event cases. Lead process and provide medical input for review of Suspected Adverse Reactions Demonstrate knowledge in pharmacovigilance and risk minimization, which includes understanding of relevant aspects of laws, regulations and guidance. Understanding and Support of the QPPV role Understanding the roles and responsibilities of the European Union Qualified Person (QPPV) and ensure their involvement in the pharmacovigilance system and processes. Ensure support and information are provided to enable the QPPV to fulfill all the QPPV legal responsibilities. Training, coaching and mentoring Provide training, coaching and mentorship to safety surveillance scientists, and other GPS Medical physicians and clinical research scientists with respect to medical aspects of safety surveillance Provide Global Patient Safety training for development and brand team physicians and clinical research scientists and other audiences (e.g. Regulatory, Lilly Medical) as appropriate. Maintain compliance with Lilly Red Book and corporate policies, Lilly Research Laboratories and Global Patient Safety curriculum map. Maintaining compliance with the Lilly Corporate Integrity Agreement. Global Patient Safety Leadership  

  • pharma
  • Management
  • Communication

Medical Affairs – Medical Writing

Eli Lilly and Company

Full time
  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects. Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration. Conduct effective document initiation meeting to ensure authoring team alignment and understanding. Build scientific-based rationale that support the purpose of more complex and/or strategic documents. Ensure data are presented in a clear, complete, accurate, and concise manner. Ensure that key data, statements and conclusions are consistent across related documents, and that statements and conclusions are integrated, accurate, balanced and supported by appropriate data. Coordinate expert/scientific reviews, collate reviewer’s comments, adjust content of document as required based on internal/external input, and prepare final version. Ensure and coordinate quality checks for accuracy. Exhibit flexibility in moving across development and preparation of multiple document types. Influence or negotiate change of timelines and content with other team members. Work with internal and external experts to develop and prepare presentations. As needed, may build and manage relationships with vendors/alliance partners.     Qualification & Experience Graduate degree with formal research component or in life sciences. Demonstrated mastery of verbal and written English skills in the medical, scientific or technical writing fields. Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, cardiovascular, immunology or endocrine expertise). Experience writing regulatory, clinical trial documents and/or publications  

  • pharma
  • Medical Writing
  • Clinical Trial

Senior Clinical Data Manager

Johnson and Johnson

Full time
  • 3+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 3+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities Sr. CDM will be involved in study related activities from the protocol design stage onwards, providing input into the study specific and/or indication specific data collection tools. Takes a leadership role with SRP/SRS to establish, align and confirm scientific clinical data review expectations for assigned trial(s). With the SRP/SRS, CRO and other functional partners in relation to CDM related activities: Reviews content for eCRF and other data collection tools Establishes conventions and quality expectations for clinical data. Set timelines and follow?up regularly to ensure delivery of all relevant Data Management milestones. Sr. CDM reviews complex scientific clinical study data, manages CDM and SRP/SRS related queries in eDC system and collaborates with Study Responsible Physician/Study Responsible Scientist (SRS/SRP). Involvement in other review activities (e.g., Coding, SAE reconciliation) is possible. Sr. CDM will lead and/or attend meetings, as appropriate. Creates the Integrated Review Plan ensuring appropriate quality, scientific content, organization, clarity, accuracy, format and consistency. Reviews related clinical data management documents. Ensures compliance with regulatory guidelines and documentation requirements. Ensures real?time inspection readiness of all assigned deliverables for the trial; participate in Regulatory Agency inspection and J&J internal audits as necessary. Plans and tracks applicable CDM deliverables. Ensures CDM deliverables are on time. Identifies and communicates lessons learned, best practices and frequently asked questions at the trial level. Identifies and participates in process, system, and tool improvement initiatives within DM.     Qualification & Experience MS degree or PhD in Science or BS/BA degree in Science with professional experience equivalent Minimum of 3 years Data Management experience, specifically data review including patient profile experience, clinical data review or significant experience with clinical data review knowledge of medical terminology. Collaboration with Clinical teams Experience in clinical drug development within the pharmaceutical industry or CRO Strong scientific knowledge (educational/professional) preferably in the relevant therapeutic area  

  • clinical research
  • Clinical Trial
  • Management

Associate Director

Novo Nordisk

Full time
  • 10+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 26, 2024
  • End Date: Apr 05, 2024
  • 10+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 26, 2024
  • End Date: Apr 05, 2024

Responsibilities We are looking for a leadership colleague that can set direction and that have a strong drive to succeed together as a team. As Associate Director, you will have the daily leadership responsibilities for the people in your team and set direction to ensure that we as a team provide best in class regulatory CMC strategies to the projects we support, thereby ensuring fast submissions and approvals globally. You will head up one of the Regulatory Affairs Chemistry Manufacturing & Control (RA CMC) teams consisting of around 12-15 colleagues. Our philosophy is clear: When you thrive and are appropriately challenged in your job, you are the best version of yourself and the most valuable colleague. Being part of an organisation that works as a strategic business partner across various parts of a product’s life cycle, you have exciting opportunities in both the department and across the company and you are expected to carry on this mindset when developing yourself as well as your team.     Qualifications & Experience Leadership experience within pharmaceutical operations or drug development, preferably from Regulatory Affairs. A strong interest in developing people and teams with a proven track record of strong results. Excellent communication skills and are known as a leader who drives change and innovation. Gained formal management training in your career. Required experience in people management. You have demonstrated your ability to lead collaborative teams and have experience with setting directions and motivating people to be ambitious in their work and interaction with stakeholders. You demonstrate a sound business understanding when you develop regulatory strategies. As a person you are ambitious. You have a proactive mindset – you take the lead on overcoming challenges and show your team the way forward. You demonstrate a sound business understanding and you believe in empowering people around you, offering them constructive feedback and guidance to improve their performance. You have a LEAN approach with a focus efficient operation. You are well-organised and have a good strategic focus. You can keep your spirits high even under pressure and as a skilled communicator you can collaborate at across organisational levels. You hold an M Pharma/or Ph.D./Bachelor in Pharmaceutical Sciences or other relevant education and have extensive experience in Global regulatory experience within CMC, including experience with European Medicines Agency (EMA)/European agencies and US Food and Drug Administration (US FDA).

  • pharma
  • bpharm
  • mpharm
  • MS Office
  • Regulatory Affairs
  • Communication

Pharmacist

Narayana Health

Full time
  • 1+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 26, 2024
  • End Date: May 26, 2024
  • 1+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 26, 2024
  • End Date: May 26, 2024

Responsibilities Develop, review, and evaluate clinical guidelines and Drug Utilization Reviews, provides consultations, develops programs, prepares articles, and conducts research.   Assess the identity, strength and purity of medications. Review prescriptions to assure accuracy, to ascertain the needed ingredients, and to evaluate their suitability. Provide information and advice regarding drug interactions, side effects, dosage and proper medication storage. Analyze prescribing trends to monitor patient compliance and to prevent excessive usage or harmful interactions. Order and purchase pharmaceutical supplies, medical supplies, and drugs, maintaining stock and storing and handling it properly. Maintain records, such as pharmacy files, patient profiles, charge system files, inventories, control records for radioactive nuclei, and registries of poisons, narcotics, and controlled drugs. Advise customers on the selection of medication brands, medical equipment and health-care supplies. Collaborate with other health care professionals to plan, monitor, review, and evaluate the quality and effectiveness of drugs and drug regimens, providing advice on drug applications and characteristics. Compound and dispense medications as prescribed by doctors and dentists, by calculating, weighing, measuring, and mixing ingredients, or oversee these activities. Offer health promotion and prevention activities, for example, training people to use devices such as blood pressure or diabetes monitors. Prepare sterile solutions and infusions for use in surgical procedures, emergency rooms, or patients' homes. Plan, implement, and maintain procedures for mixing, packaging, and labeling pharmaceuticals, according to policy and legal requirements, to ensure quality, security, and proper disposal.     Qualifications & Experience Able to work accurately and with minimal supervision. Ability to comprehend written instructions given by the Doctors and the other related departmental personnel. Ability to plan & organize ones work schedule effectively. Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel. Affinity to work in team. Enthusiasm. Open-mindedness.

  • pharma
  • pharmacovigilance
  • MS Office
  • Management
  • Communication

Director Patient Safety

AstraZeneca

Full time
  • 10+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 26, 2024
  • End Date: May 26, 2024
  • 10+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 26, 2024
  • End Date: May 26, 2024

Responsibilities As a Director of Patient Safety, you will manage a team of Patient Safety staff locally. You will develop strategies and objectives for Patient Safety in your area of responsibility, ensuring alignment with broader AstraZeneca goals. You will maintain a high degree of understanding and awareness of internal and external trends influencing the PS domain, sharing this knowledge with your team. You will build networks with other teams and external stakeholders to learn about new developments, leverage opportunities, and share best practices. You may manage or support projects to improve processes within Patient Safety or develop and introduce new technologies and approaches at the national, regional, or global level.     Qualifications & Experience Medical degree/ Qualified to degree level in biosciences or an equivalent healthcare or pharmaceutical industry background, with proven competency in patient safety/clinical development Experience in Patient Safety in the pharmaceutical industry Excellent communication skills Project management experience Knowledge of relevant legislation and developments in the Pharmaceutical industry Medical or other life science degree or appropriately qualification as Health Care Professional PV Professional (Scientist) Experience in either writing Risk Management Plans and assessing risk mitigation activities or in translating preclinical safety experience to humanPh.D. in a scientific discipline Expert reputation within the business and industry Extensive knowledge of the latest technical and regulatory expectations Line management experience

  • pharma
  • MS Office
  • Regulatory Affairs
  • Management
  • Communication

Ayurvedic Doctor Consultant

Kapiva

Full time
  • 0-1 years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 25, 2024
  • End Date: May 25, 2024
  • 0-1 years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 25, 2024
  • End Date: May 25, 2024

Responsibilities Conduct comprehensive online Ayurvedic consultations with patients, including diagnosis, treatment, Suggesting Investigations, and follow-up advice. Develop personalized treatment plans based on Ayurvedic principles, considering patient's health conditions and suggestive reports. Offer lifestyle and dietary recommendations under Ayurvedic practices to help patients achieve optimal health. Maintain accurate and detailed patient records in compliance with confidentiality and data protection laws Handling BAU responsibilities like ensuring Standard SOPs are followed. Participate in continuous learning and training to stay updated with the latest advancements in Ayurveda and telehealth for the benefit of the organization. Collaborate with the teleconsultation team and contribute to the development of the platform by providing insights and feedback. Assisting Market research teams with sharp insights into doctor <> patient consultation needs.   Qualification & Experience B.A.M.S. degree from a recognized Ayurvedic college. Valid registration with a state or national Ayurvedic board/council. Minimum of 2 years of clinical experience in Ayurveda, with a strong understanding of Ayurvedic diagnostics and treatment protocols. Freshers can apply for a 3-round selection process which the team performs for young talents.  

  • clinical research
  • Operations
  • Inspection

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