Responsibilities Assists the physician with cardiac catheterizations. Demonstrates competency in sterile technique preparing for procedure including scrubbing, applying surgical gown, gloving, draping and set up of instrument table. Under the direction and supervision of the physician administers medications pertinent to cardiac catheterization.  Demonstrates competency in Holter monitor - initialization, application and correct removal. Scans Holter monitors accurately and efficiently, identifying, documenting, and reporting any significant/life threatening arrhythmias. Operates and ensures the quality control of all equipment utilized in the cath lab.   Qualification & Experience Diploma in Cath-Lab Technician from State Medical Faculty of West Bengal Minimum 5 years experience required in similar profile    

Responsibilities Provide efficient and effective nursing care to patient. Maintain surgical services in accordance with competency standards. Complete all physician orders, administer medications, and conduct treatments and tests for patients in a timely manner. Assist with patient care in recovery room, procedure room and operating room. Execute proper use, care and handling of surgical equipment to ensure safety of operating staff and patient. Maintain current and in-depth knowledge of sterile techniques. Prepare operating room with surgical equipment, sterile, linens and supplies that will be needed during surgery. Maintain order and cleanliness in operating room. Prepare patients including cleaning and disinfecting body areas for surgery. Prepare timely and accurate records of patient history and recovery charts.   Qualification & Experience Bachelors/Masters in Nursing Minimum 5 years of experience required in similar profile  

Responsibilities Providing assessment, monitoring and intervention for cardiac procedures, such as coronary stents, right heart catheterization, angioplasty and pericardiocentesis. Administering oral and intravenous medication to patients. Managing patients under sedation to watch for adverse reactions Educating patients and their families regarding surgical site care, lifestyle, medications and other postoperative information.   Qualification & Experience B.Sc./M.Sc. in Nursing G N M Minimum 5 years experienc

Responsibilities Scientific Expertise Developing and maintaining an in-depth understanding of the company's products, therapeutic areas, and relevant scientific research. Staying updated on the latest medical and scientific advancements, clinical guidelines, and treatment protocols. SL & KDM Engagement Building and maintaining relationships with Scientific Leaders (SLs), Key decision makers (KDMs) healthcare professionals, and academic institutions. Engaging in scientific discussions, presenting clinical data, and providing educational support to KOLs regarding the company's products and therapeutic areas. Support to medical strategy In alignment with the line manager, provide strategic inputs, and expertise, to product management towards ethical promotion of assigned products Medical Education Providing scientific and medical education to internal stakeholders, including sales teams, marketing teams, and other cross-functional colleagues. Collaborating with the Medical Affairs team to develop and deliver training materials, presentations, and scientific symposia. Scientific Exchange Facilitating scientific exchange and knowledge transfer between the company and external stakeholders. Participating in medical conferences, advisory boards, and scientific meetings to gather insights, share data, and contribute to the scientific community. Clinical Data Communication Interpreting and communicating clinical trial data, real-world evidence, and other scientific information to healthcare professionals, regulators, and other relevant stakeholders. Ensuring accurate and compliant dissemination of scientific information in accordance with regulations and company policies. Clinical Research Provide medical support for local studies, including need-based visits to identify study sites Lead Investigator Initiated Trials Cross-functional Collaboration Collaborating closely with cross-functional teams, including Clinical Development, Regulatory Affairs, Marketing, and Market Access, to provide scientific input, support clinical trial design, contribute to regulatory strategies, and align on medical communication plans. Facilitate access to scientific leaders as appropriate. Support as well as own medical initiated projects in line with therapy area that would involve a strong stakeholder interface Provide scientific support to sales team Medical Information Addressing medical inquiries and providing timely and accurate responses to healthcare professionals, patients, and other stakeholders. Ensuring that medical information materials, such as medical letters and FAQs, are up to date and compliant. Sales Force Training Provide medical training to sales colleagues on the therapy areas assigned Assist in pre-launch and launch training to sales staff for new products. Compliance Adhering to relevant legal, regulatory, and compliance guidelines, including the organization's code of conduct and industry-specific regulations. Ensuring all activities and interactions are conducted ethically and in compliance with applicable laws and regulations. Overall, RMA in Medical Affairs acts as a scientific expert and liaison between the company and external stakeholders, playing a crucial role in building scientific credibility, fostering relationships, and supporting the company's strategic objectives in the healthcare industry.   Qualfication & Expereience Educational Background A strong academic background in life sciences, such as a medical degree (MD), doctorate (Ph.D.), or pharmacy degree (Pharm.D.). Other relevant degrees in biology, pharmacology, or related fields may also be considered. Industry Experience Prior experience in the pharmaceutical, biotechnology, or medical device industry is often preferred. This could include experience in clinical research, medical affairs, or related roles that have exposed the candidate to scientific and medical aspects of the industry.  

Responsibilities Develop high-quality written material (manuscripts, web content, posters, brochures, flyers, etc.) to support the product portfolio. Reviews and evaluates scientific data and technical documents to develop written material. Assists the marketing team in conducting content-need analysis. Provide informal guidance and support to new team members, fostering a collaborative and inclusive work environment. Ensures compliance with quality processes and requirements for assigned documents. Provides input on and independently develops best practices, methods and techniques for achieving optimal results. Review scientific content and offer constructive feedback, drawing upon your knowledge and expertise in biological sciences. Interact with cross-functional teams and customers at multiple locations globally.     Qualification & Experience PhD in Biological sciences, biotechnology or immunology, or a related discipline with 3+ years of experience with bioprocessing. 2+ years’ experience in content creation in an industry setting. Experience in a regulated environment desired.  

Qualification & Experience Graduate, preferably with a background in the hospital industry. Experience: 3 to 10 years of experience required. We are seeking smart, young, and energetic candidates.   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities The Medical Affairs Systems Admin will manage Field Medical colleague HCP profiles in 50 OneMed markets and work closely with Data Stewardship team to ensure data fields are maintained effectively. This role will work closely with the US and Global master data management (MDM) teams to ensure that the relevant and up to date HCP databases are being correctly configured and managed as the authoritative source of HCP profile data within OneMed (CRM). This colleague will coordinate and monitor activities between Digital and the MDM teams, to ensure overall quality, including up to date and complete HCP information are reflected within our systems, to minimize partial data records, duplications, or outdated information. The Medical Affairs Systems Admin will maintain system user access and user profile management for OneMed, Veeva Link, mGCMA, Adobe, Triage, leveraging Request manager and Pfizer Align. This role will perform regular management and monitoring of medical user’s data within Pfizer Align, validating that data is synced across our Medical Systems portfolio, and mirrors data from our PX systems. This data includes team structures, user’s profiles, reporting lines, and product allocations. The Medical Affairs Systems Admin, working closely with the OneMed support team, will verify that there is a full harmonization between the medical user information within Pfizer Align and what is required for the creation and management of the respective user accounts in OneMed (CRM) This role will act as the focal point and the subject matter expert for Pfizer Align, providing ongoing support and training whenever a change within the Medical Affairs organization structure is required to be performed, and reflected in our systems. This colleague working closely with the Pfizer Triage team will verify that the data is up to date and consistent, ensuring automatic data flows between the three systems – Pfizer Align, Pfizer Triage and OneMed (CRM). The Medical Affairs Systems Admin will review and approve/reject user access requests within Request Manager and work regularly with various system support teams on maintaining the request forms so they reflect exactly all the required information needed to create a new user or change in user role. This colleague will manage the Global medical subjects/topics/products catalog, overseeing and managing all change requests and adhering to our governance process. This role will manage the end-to-end process of adding/renaming/disabling new products across all system platforms. This includes the initiation of requests, thorough analysis of the data and action needed for each platform, submitting tasks to various support teams (mGCMA, OneMed, Adobe, Pfizer Triage, Pfizer Align), and overseeing testing and monitoring its completion into production. The Medical Affairs Systems Admin is responsible for managing complex requests of renaming values and collaborating with different stakeholders to ensure quality standards, while making sure it is completed simultaneously within all systems within the Medical Affairs portfolio. This colleague will work closely with the global Taxonomy team (Commercial) to verify that the same principles, naming conventions and data values are used across all platforms leveraged by Medical and Commercial.     Qualification & Experience BA/BS Required; graduate degree or equivalent experience preferred 5+ years in the pharmaceutical industry, with 3+ years in Medical Affairs technical roles preferred Well experienced in operating & supporting Medical Affairs technology platforms Excellent communication and analytical skills  

Responsibilities The specific job duties of a Senior External Vendor Data Manager may include, but not limited to: Serves as the subject matter expert for the setup of external vendor management and reconciliation processes at the study and/or portfolio level. Ensure electronic vendor data contains all protocol-specified parameters, is in the correct format, and data populates in the specified fields correctly. Assist in the development of the Data Transfer Agreement and Data Transfer Specifications for vendor data transfers. Contribute to the standardization of data type specifications. Perform validation of the electronically transmitted data to ensure compliance with the expected data/file formats. Perform quality control of data discrepancies generated by study-specific edit checks for External data. Assist with the creation of External Data edit checks, External Data status reports, and External Data reconciliation listings. Perform validation and quality control of External Data status reports and External Data reconciliation listings. Identify data transfer issues and provide recommendations for solutions. Interact with Lead Clinical Data Manager and Data Management team to resolve discrepant information, issues identified with External Data edit checks, External Data status reports, and External Data reconciliation listings. Contributes to the creation of External Data Guidance documentation. Train and mentor team members involved in external data reconciliation process. Actively participate in external data process enhancements. Perform other duties as required by the Department.     Qualification & Experience College graduate with life science, computing, or nursing qualifications or equivalent 3 to 4 years experience required Minimum of 6 years of experience and/or demonstrated an aptitude for external data management work, preferably within the oncology therapeutic area.  

Responsibilities The specific job duties of a Clinical Data Manager II may include but are not limited to: For specified projects performs start-up activities including: Developing data management guidelines and study documentation Assists in developing core study documents for data management including DMP, DVP, CRF completion guidelines, and other study documentation as needed Review of CRF design against protocol Review of database setup For specified projects performs some data management activities as detailed below and performs activities in accordance with our SOPs, Good Clinical Practice, ICH Guidelines and study documentation. Study status tracking and associated metrics Data Entry Review and reconciliation of data listings Identification of data issues and query generation Updating of database with query resolutions (paper studies only) Ownership and proactive management of the data reconciliation activities documented in the DVP, DMP, etc. Provide input for Database closeout and lock activities and timelines Archiving of critical documents on an ongoing basis Provide support to deliver DM specifications for CRF counts and associated details for proposal needs. Awareness of the CAPA process and provide input for audit responses regarding assigned tasks Participate in User Acceptance Testing for assigned projects For specified projects performs study finalization activities including: Database close-out Critical item review and Quality control support as needed, per platform Data review and reconciliation Quality Control Archiving Supports and tracks budget adherence in cooperation with Finance to ensure the assigned studies are meeting targeted margins and utilization Continuous improvement of departmental processes and procedures to ensure DM is consistently maximizing efficiencies, leveraging technology and incorporating innovation to optimize delivery Maintains working knowledge of regulatory requirements/guidance as well as industry leading best practices to ensure Clinipace DM procedures are in line with industry expectations Other duties as assigned   Qualification & Experience College graduate with a life science, computing or nursing qualification or 3 to 4 years equivalent experience.Experience Minimum of 3 years of experience with demonstrated experience supporting data management work. Experience working in pharmaceutical and/or Contract Research Organization (CRO) industry preferred  

Responsibilities The specific job duties of a Clinical Data Manager III may include but are not limited to: For specified projects performs start-up activities including: Developing data management guidelines and study documentation Review of CRF design against protocol Lead study developing core study documents for data management including DMP, DVP, CRF completion guidelines, and other study documentation. Activities include design, database structure, document creation; including approval For specified projects performs data management activities as detailed below and performs activities in accordance with our SOPs, Good Clinical Practice, ICH Guidelines and study documentation. Study status tracking Review of data listings Identification of data issues and query generation Updating of database with query resolutions (paper studies only) Processing and reconciliation of external data including SAE reconciliation Ownership and proactive management of the data reconciliation activities documented in the DVP, DMP, etc. Provide input for Database closeout and lock activities and timelines Archiving of critical documents on an ongoing basis If assigned the Lead Data Manager role, act as key data management contact for the project. Awareness of the CAPA process and provide input for audit responses regarding assigned tasks Proactively manage project quality through supervision and quality control of team members’ work. Proactive participation in appropriate sponsor/project team meetings. Active involvement in departmental and organizational meetings and initiatives. Develops and documents departmental procedures. Training and Mentoring of team members in accordance with established departmental procedures. Supports and tracks budget adherence in cooperation with Finance to ensure the assigned studies are meeting targeted margins and utilization Continuous improvement of departmental processes and procedures to ensure DM is consistently maximizing efficiencies, leveraging technology and incorporating innovation to optimize delivery Maintains working knowledge of regulatory requirements/guidance as well as industry leading best practices to ensure Caidya DM procedures are in line with industry expectations Indirect supervision of the work of junior members of the project team. Other duties as assigned   Qualification & Experience College graduate with a degree in life science, computing or nursing qualifications preferred; or 5 to 6 years equivalent experience. Experience Minimum of 5 years of experience and/or demonstrated aptitude for data management work. International team experience preferred. Experience working in pharmaceutical and/or Contract Research