ResponsibilitiesAreas of Expertise: EEG, EMG, NCV, VEP, Blink Reflex, RNS, etc. Neurologist appointments for OPD, assisting in IPD neurology investigations.Qualification & ExperienceEducationAn Associate or Bachelor’s degree in Neurodiagnostic Technology or a related health care field is typically requiredExperienceFresher/6 months-1 year experience in hospital only.Work ExperienceFresher/6 months-1 year experience in hospital only.QualificationDiploma/ BSC Neurodiagnostic Technology.

ResponsibilitiesData Management: Maintaining both electronic (EHR) and paper records, ensuring they are complete, accurate, and up-to-date.Confidentiality & Compliance: Ensuring all records comply with legal, ethical, and hospital policies (e.g., HIPAA).Record Retrieval: Efficiently locating and retrieving records for authorized medical staff.Coding & Documentation: Assigning medical codes (ICD, CPT) for diagnoses and procedures for billing and research.Auditing: Reviewing records for completeness and accuracy.Reporting: Compiling data for hospital statistics, such as admissions, discharges, and deaths.Male candidate preferring.Document hardware configurations, maintenance, and procedures.Qualification & ExperienceEducationDiploma in Medical Records Technology or a related field.ExperienceMinimum 1 yearQualificationDiploma in Medical Records Technology or a related field.PreferredBachelor’s degree in Health Information Management, Health Administration, or a related field.

ResponsibilitiesIntegrate the company’s products into hospital formulary lists and prepare technical specifications for auctions and quotations.Maintain and systematically update the customer database, including hospitals, polyclinics, and distributors.Execute marketing strategies by distributing promotional materials and funds in compliance with guidelines.Monitor competitor product performance and update the team on market dynamics.Mentor newcomers, provide peer support, and act as a buddy within development areas.Ensure synchronization of reports and plans according to SFE requirements.Serve as a deputy Key Account Manager in their absence, support the team, and work with distributors.Build relationships with KOLs through presentations and front-end customer interactions.Qualification & ExperienceEducational Qualification: Graduation degree in any discipline; medicine/pharma is preferredMinimum Work Experience: 3+ years within B2B pharma or medical equipmentSelling TechniquesDigital StorytellingAccount ManagementBid ManagementContract ManagementCustomer Relationship ManagementOrder Fulfilment

ResponsibilitiesManage assigned mailboxes, including inbox triage of client communication, inbound reports, and internal case processing communications. Perform Duplicate searches and complete initial book-in as required. Screen and redact the source documents for PHI as per company procedures. Facilitate literature related activities as needed. Initial triage of regulatory authority database searches. Send draft reports to clients for review as needed. Enter basic data into safety database as required such as identifiable patient, report, suspect drug, and adverse event. As applicable perform full data entry into safety databased with proper experience and training. Other duties as assigned.Qualification & ExperiencePost-secondary education.Preferred: one year of industry experience.

Responsibilities• You will be responsible for the engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan?• You will be responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects??• You will be a therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients’ treatment trends and studies in the therapeutic areas in which the Company is?? involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart?• You will be responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals??• You will have to represent the organization in various internal & external scientific platforms??• You will have to gather deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams.??• You will need to proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan?• You will be receiving and processing scientific information requests received from physicians?• You will have to ensure that all activities in the region are conducted in alignment to organisation’s COBE (Code of Business Ethics) Policy and compliance guidelines.• You will need to collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in reputed journals.• You will be responsible for devising an optimal training plan to ensure the flow of the latest medical developments to the sales and marketing teams.• You will jointly be responsible with the therapy area lead to support optimal patient outcomes through communication of data, information, knowledge, and insights in support of healthcare professional needs and organizational goals.• Representing the organization in various internal and external scientific platforms will be among your responsibilities.• You will be responsible for developing the Medical Affairs strategic plan for identified therapeutic areas and products.• Your ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest will be vital.• You will be responsible for identifying knowledge gaps, practice gaps, and data gaps and developing strategic medical action plans, including but not limited to medical education, product education, evidence generation, and special projects, will fall under your responsibility.• Collaborating with thought leaders to conduct therapy-specific reviews, meta-analysis, case studies, case series, patient-reported outcomes, and publishing them in reputable journals will be part of your role.• Handling complex questions from healthcare professionals related to GGI products or disease areas to satisfaction will be a key responsibility.• You will be responsible for ensuring that all activities in the therapeutic area are conducted in alignment with Dr. Reddy's COBE (Code of Business Ethics) Policy and compliance guidelines will be essential.• You will be responsible for ensuring that all promotional, physician, and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy's Promotional Material approval policy.• As a product pipeline champion, you will have the ability to identify unmet needs through active stakeholder interactions and actively contribute to the new product ideation and development of differentiated products.Qualification & Experience• Educational Qualification- MBBS with full time post-graduate qualification of at least 2-years’ duration in any discipline of medicine/ M.B.B.S with M.B.A. from a reputed institute • Minimum work experience- Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs.• Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data?• Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship?• Experience with complex business environments preferred?• Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.

Responsibilities• You will be responsible for the engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan?• You will be responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects??• You will be a therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients’ treatment trends and studies in the therapeutic areas in which the Company is?? involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart?• You will be responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals??• You will have to represent the organization in various internal & external scientific platforms??• You will have to gather deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams.??• You will need to proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan?• You will be receiving and processing scientific information requests received from physicians?• You will have to ensure that all activities in the region are conducted in alignment to organisation’s COBE (Code of Business Ethics) Policy and compliance guidelines.• You will need to collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in reputed journals.• You will be responsible for devising an optimal training plan to ensure the flow of the latest medical developments to the sales and marketing teams.• You will jointly be responsible with the therapy area lead to support optimal patient outcomes through communication of data, information, knowledge, and insights in support of healthcare professional needs and organizational goals.• Representing the organization in various internal and external scientific platforms will be among your responsibilities.• You will be responsible for developing the Medical Affairs strategic plan for identified therapeutic areas and products.• Your ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest will be vital.• You will be responsible for identifying knowledge gaps, practice gaps, and data gaps and developing strategic medical action plans, including but not limited to medical education, product education, evidence generation, and special projects, will fall under your responsibility.• Collaborating with thought leaders to conduct therapy-specific reviews, meta-analysis, case studies, case series, patient-reported outcomes, and publishing them in reputable journals will be part of your role.• Handling complex questions from healthcare professionals related to GGI products or disease areas to satisfaction will be a key responsibility.• You will be responsible for ensuring that all activities in the therapeutic area are conducted in alignment with Dr. Reddy's COBE (Code of Business Ethics) Policy and compliance guidelines will be essential.• You will be responsible for ensuring that all promotional, physician, and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy's Promotional Material approval policy.• As a product pipeline champion, you will have the ability to identify unmet needs through active stakeholder interactions and actively contribute to the new product ideation and development of differentiated productsQualification & Experience• Educational Qualification- MBBS with full time post-graduate qualification of at least 2-years’ duration in any discipline of medicine/ M.B.B.S with M.B.A. from a reputed institute • Minimum work experience- Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs.• Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data?• Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship?• Experience with complex business environments preferred?• Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.

Responsibilities Responds to unsolicited consumer, health care professional and other external customer requests for medical and safety information received via telephone, website/e-mail, letter, fax, and scientific meetings on behalf of ProPharma’ s pharmaceutical clients.  Provides labeled and unlabeled medical/safety information responses in accordance with regulatory requirements, industry standards and client and ProPharma internal policies and practices.  Accurately identifies, documents and reports adverse events, pregnancy reports, special situation events and product complaints in a clear and concise manner per government regulations, ProPharma Standard Operating Procedures (SOPs) and client Working Practices (WPs).  Ensures tasks are completed within the deadlines documented in the agreed ProPharma SOPs and WPs.  Formulates and provides accurate responses utilizing approved labeling and company standard responses, published literature and other data. Assists with writing custom medical information responses utilizing this data.  Logging all enquiries handled in an accurate, comprehensive, and timely fashion into Inquiry Handling Systems. Quality Assurance  Maintains quality in all areas of the job, including performing quality checks on Adverse Events, Product Quality Complaints, correspondence, and enquiries logged into the Inquiry Handling Systems General  Provides after-hours coverage on a rotated basis subject to business requirements.  Adheres to company and country-specific privacy policies, ensuring any confidential information or personal data related to ProPharma and its clients is managed in accordance with Data Privacy regulations described in ProPharma SOPs and the Confidentiality Statement within the Contract of Employment.  Complies with the Company’s health and safety policies.  Other activities as assigned as delegated by the ManagerQualification & Experience Life science degree OR Nursing degree (RN/BS/BA/MS) OR Pharmacy degree  Excellent verbal and written communication skills, including proofreading, professional telephone etiquette and empathetic customer service skills.  Ability to write in a fluent and grammatically correct manner in the target language for the role  English language proficiency. Japan-based roles only: TOEIC 800=  Working knowledge of medical terminology, pathophysiology, pharmacology, regulations and industry standards.  Strong cognitive abilities, including verbal reasoning, critical thinking and analytical ability.

ResponsibilitiesResponsible for overseeing and performing daily case processing of adverse event cases (clinical trial and/or post marketed), including coding using MedDRA, determining seriousness and expectedness at the event and case level. Perform case follow up activities such as identification of information to be collected during follow-up. Creating and reviewing case narratives. Providing client notifications as required for case management. Supporting and contributing to the development of training materials and training delivery. Highlight areas of concern/discrepancies to the Principal PV Specialist, Case Processing and/or Manager, Case Processing when related to ICSRs. Acquire and maintain an up-to-date knowledge of global safety regulations for medicines. Peer reviews of cases for quality, consistency, and accuracy. Provide oversight and direction of PV deliverables as a PV subject matter expert as needed. Perform Health Care Professional (HCP) review (as required). Mentors and trains less experienced staff. Other duties as assigned.Qualification & ExperienceRequired: a Bachelor's degree in life sciences. Preferred: an advanced degree, RN, RPh, PharmD or equivalent.

Responsibilities Triage incoming reports for completeness, legibility and validity  Bookin and Data entry of case reports into safety database  Request follow-up and perform query management  Coding of data in the safety database  Writing case narrative.  Perform Literature searches  Participate in client meetings as required  Preparation for, participation in, and follow-up on audits and inspectionsQualification & ExpeirneceQualification: B.Pharm/M.Pharm/Pharm D Experience: 1– 3 years

Responsibilities Draft PADER aggregate reports as per the aggregate reporting schedule. Prepare line listings and tabulations for inclusion in the PADER report. Develop and maintain the PADER report calendar and schedule. Coordinate and resolve queries with cross-functional teams before finalizing line listings, addressing any issues identified in draft cases. Communicate with cross-functional teams to obtain required inputs and resolve queries efficiently. Archive all PADER-related information in the designated shared drive. Submit PADER documents and reports within specified timelines, ensuring compliance with internal and regulatory submission requirements. Prepare and review SOPs and work instructions in alignment with ICH-GCP, GVP modules, and FDA guidelines. Provide training to junior associates on PADER report preparation and processes. Support client audits and regulatory authority inspections as needed.Qualification & Exppeirnece4–6 years of experience in aggregate report preparation for quality control roles. 3–4 years of experience in aggregate report drafting roles. Educational Qualifications M.Pharm or Pharm.D candidates are preferred.