Pharmacovigilance Jobs

A Junior Doctor is responsible for providing medical care to patients, including diagnosing and treating various medical conditions. They must also perform medical procedures, prescribe medications, and educate patients about their health. Key responsibilities of a Junior Doctor include:- Conducting patient consultations and physical examinations- Ordering and interpreting diagnostic tests- Developing treatment plans and providing ongoing care for patients- Collaborating with other healthcare professionals to ensure coordinated care- Keeping detailed and accurate medical records

Review medical records and translate them into standardized codes using ICD-10, CPT, and HCPCS coding systems. Collaborate with healthcare providers to obtain accurate information for coding purposes. Ensure all codes are compliant with healthcare regulations and insurance requirements. Assist in maintaining accurate documentation and coding practices to meet healthcare standards. Communicate with the coding and billing departments to resolve discrepancies or issues. Stay updated with changes in medical coding practices and healthcare regulations. Educational Background: Nursing degree (RN, LPN, or related nursing qualifications). Certification (Preferred, but not required): Certification in Medical Coding (e.g., CPC, CCS) or willingness to pursue certification after employment. Technical Skills: Basic knowledge of medical terminology, anatomy.Why Join Us? Training & Development: Comprehensive Medical Coding training will be provided to help you gain expertise in medical coding. Career Growth: We offer opportunities for career advancement and professional development within the healthcare industry. Work-Life Balance: Flexible working hours and a supportive environment. Competitive Compensation & Benefits: Health insurance, paid time off, and other benefitsQualificationsPharmacy : B.Pharmacy / M.Pharmacy / Pharmd Life Sciences : Microbiology,Biotechnology Biochemistry Botany zoology chemistry BioInformatics Medical : MBBS BDSParamedical : BHMS BAMS GNM ANM Nursing MLT Food and Nutrition

Job Description: - Should have knowledge about Adverse Events (AE), PV and Quality check. Adverse Event reporting and its source data collection and Verification Adverse Event reconciliation Listening of sample calls and verifying with respect to AE reporting. Review of sample calls of FC, PTC Interaction summary with respect to AE reporting. Sample Audit of Rx with respect to AE reporting. Preparing report basics all Audit parameters and sharing with HCAH Management & Client Custodian of Adverse Event SOP and Tracker Conducting Process training and Pharmacovigilance / Adverse Event Reporting Should be responsible for checking all AEs, AE tracker, Zelthy hygiene check and Coordination with PV team. Should be responsible for doing Call quality, Documents check and PV check.

Position: Research And Development ApprenticeshipEligibility: LGBT Applicants Only + B.Pharm/M.Pharm (2022, 2023 or 2024 pass outs) + Bangalore City candidate***The above 3 parameters in Eligibility will be considered ONLY***Qualification: (2022, 2023 & 2024 Pass Outs) B. Pharm / M. PharmStipend: INR 25,000 per month (in hand)Duration: 12 monthsCTA: Depending on performance maybe be converted into full time resources at the end of the internship periodWork Timing, General Shift: 9AM to 5 PMLocation: Bengaluru OnlyWho Can Apply - LGBT+ (Lesbian, Gay, Bisexual, Transgender+) Pharma Job Seekers who are based in and around Bengaluru only Role Requirements-Good English language skills written and verbal particularly in scientific/medical terminologyAbility to evaluate data and draw conclusions with appropriate guidance from senior team members or managerGood attention to detailGood interpersonal, presentation and communication skillsService-oriented attitude and ability to be a team player and interact effectively with all levels of personnel in an interdisciplinary and matrix environmentComputer proficiency, IT skills, the expertise and ability to work with web-based applicationsGood level of flexibility and ability to prioritize workIf you belong from LGBT Community then please send CVs at pamela@thepridecircle.com

Vacancy in Pharma and Chemical IndustryQualification - Bsc / Msc chem, BE/Btech - Chem / Petrochem / BpharmMale and Female Can ApplyWork Location - ChennaiSalary - NegotiableDesignation - QC / P Chemist / Lab / Clinical Research / RND

Responsibilities Support to manufacturing for achieving performance targets. Lead the technology input into the root cause analysis of complex process/engineering issues. Define improvements and upgrades in existing processes / equipment / technologies to reach higher capacities, higher process efficiencies. Identify, justify and prioritize plant improvements for PIOs, CAPEX, REVAMP projects, including major projects (new plants) and support:- Review process-engineering documents as part of Basic Engineering and Detail Engineering.- Evaluation of external technologies for improvement schemes as well as for new plants- Review of Process Design Package of Technology Licensors- Preparation of Design Basis documents and Process Design Packages for in-house developed / conceptualized improvement schemes- Participation in PHA reviews (HAZID / HAZOP)- Evaluation of vendor technical proposals including cost-benefit analysis - Review of vendor documents post order.- Preparation / review of Operation Manuals, SOPs and SOCs. Catalyst / chemicals / additives / fuels evaluation. Audit and benchmark plant/ product / energy performance. Ensure achievement of set milestones for pilot / scale up studied. Anticipate constraints / trends in technology and product application range and review and recommend alternatives for implementation. Participate in commercial plant trial. Develop, validate, customize & maintain simulation / APC models. Preparation of final technology comparison reports. Participate in PSM activities. To coach/mentor and support the on-boarding and development of the GETs (technology)Skills: Has a thorough knowledge of chemical engineering, codes, and standards, and of process technology in respective domain. Works independently, takes independent actions on technical issues within the field of expertise. Relevant industrial experience (4-8 years) with good technical background and good communication skills.

Review and execute physicians prescriptions checking their appropriateness and legalityOrganize the pharmacy in an efficient manner to make the identification of products easier and fasterMaintain full control over delivering, stocking and labeling medicine and other products and monitor their condition to prevent expiring or deteriorationListen carefully to customers to interpret their needs and issues and offer information and adviceProvide assistance other medical services such as injections, blood pressure/ temperature measurements etc.Prepare medicine when appropriate using correct dosages and material for each individual patientKeep records of patient history and of all activities regarding heavy medicationKeep abreast of advancements in medicine by attending conferences and seminars and collaborating with other healthcare professionalsComply with all applicable legal rules, regulations and procedures

Essential Functions Review and assure the quality, integrity, accuracy, and completeness of clinical trial data based on project specific guidelines. Develop and maintain a library of effective data quality checks. Review data exports and reports to identify, investigate, and reconcile data discrepancies with Clinical Operations staff and/or clients Data Managers. Prepare, review, and upload appropriate Data Management documents to the Trial Master File Perform thorough development testing of the datasets prior to release to production, inclusive of creating test scripts and execute testing as applicable. Author Data Transfer specifications (DTS) for incoming and outgoing data files. Collaborate effectively and build productive relationships across the global operations team. Performs other job-related duties as assignedQualifications 3+ years of data management experience in the clinical trials industry BS/BA degree or professional experience equivalent. Demonstrated successful experience in all relevant clinical data management activities in a Pharmaceutical or CRO setting. Working knowledge of clinical trial research, including FDA, GCP/ICH guidelines, GDPR, CDISC/SDTM standards and 21 CFR Part 11 Experience working with EDC systems, e.g., Medidata Rave or Oracle Inform Familiarity with industry wide coding dictionaries such as MedDRA is a plus Experience with relational databases and XML a plus Excellent written and oral communication skills. Excellent analytical and problem-solving skills Ability to function independently. Ability to prioritize and handle multiple tasks and projects concurrently

The Nicton team is a leading Russian R&D company dedicated to its business in alternative nicotine use. We develop new products in the field of pharmacology, dietary supplements and food components, developed agriculture and alternative nicotine consumption.We are looking for Pharmacist specialist who can help register for Wholesale Drug License (20B & 21B).The Company offers: An easy supporting job for Company; Official one-time payments for services; Compensation of transport costsKey duties: Provide competent support for getting license 20b & 21b (Wholesale drug license); Sign the legal documents which require pharma degree; Personal attendance of meeting with authorities if necessary; Providing yourself with official digital signature and signing the documents according to the official procedure of getting license;Requirements: 1-2 years of relevant job experience in pharma field; At least bachelor degree of pharma (B-doc pharma or M-doc pharma); English language level: Elementary; Registered with authority (having an official number); Location in Delhi.

A pharmacovigilance associate ensures compliance with applicable regulations or standard operating procedures; specialises in drug safety management, clinical trials and medical supervision. Responsible for conducting, monitoring or reporting regular pharmacovigilance developments and supervising the processes related to ensuring drug effectiveness and avoiding adverse effects or side effects of marketed pharmaceutical products among the general population in research trials and hospitals.Pharmacovigilance associate aim at reducing the risks associated with administering and prescribing drugs along with improving safety and treatment outcome in patient care. The role includes activities of important case report follow-up; processing and writing adverse event programs; serving link between the company, healthcare experts and patients for delivery of valid information on product safety; Conducting and supervising regular pharmacovigilance processes; attending several product safety meetings and adding functionality to product sa

Collaborate with physicians to discuss potential incompatibility issues with patient prescriptionsMaintain accurate inventory of medicationsOffer information to assist patients in understanding how to properly take their prescribed medicationsWork with the pharmaceutical staff to maintain a clean, customer-friendly workplaceAssist patients in solving problems, such as identifying old medication or finding an over-the-counter solution to minor health issues

Scientific Literature SearchWet Lab Work - Take lab trails.R&D Documentation Work Candidate should have sound experience in Food beverages (Liquid formulations)/ Clinical Nutrition/ Ayurvedic formulationsRequired Qualifications: B.tech/M Sc. (Food Science and Technology)

Regulatory Affairs ExecutiveLocation: Vadodara, GujaratMust have Experience in Pharma Industry Must have experience in handling regulatory affairs for ROW market mainly Central and Latin America and Africa for Pharma Formulations. Preparation, Compilation & Review of Registration documents that include Administrative & Technical. Reviewing the technical documents provided by QA, QC, Production. Providing them the report of shortcomings & ensures them to correct the documents. Handling RFIs (Requested Further Informations) queries raised by Importer/ Agent/ Regulatory authorities during evaluation of technical data. Coordinating concerned (QA, QC, Production, Packing & Purchase) departments in the process of sample preparation. Coordinate & submission of CTD/ACTD/Country Specific Dossiers/DMF (OP) to regulatory agencies. Coordinate & provide support to team for preparation and dispatch of regulatory documents & dossiers in agreed time-frames. Responsible for planning, coordinating and managing day to day regulatory affairs activities in a timely manner. Providing technical knowledge of the data used in CTD, ACTD & Dossiers to members of regulatory team. Fill up customer questionnaires by collecting information from various concerned departments. You should be good in man - management & co - ordination with all the departments Interact with various administrative, legal & factory departments to collect documents required for regulatory compilation on time. Maintenance of the complete history of each drug product

Position Clinical Research CoordinatorQualification B.PharmExperience - Above 1YearsTiming - General ShiftSalary Based upon PerformanceLocation ChennaiLicence: Pharmacy Lice(Only B. Pharm is eligible for this Job)Job Description Clinical Research Coordinator: To have the good knowledge of regulations and GCP guidelines. Ability to communicate properly between the physician, patient & the site head. Assist the Site Head in the managing the Site to ensure ethical conduct of research activities. Assist Site Head in evaluates protocols, policies and procedures regarding research projects and studies. Maintains pertinent records and documentation. Provide guidance to CRC in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures. Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents. Oversight of Site Initiation Visit, Monitoring Visits, Site Closeout Visit. CRF, e-CRF entry, Data Query resolution. Assist the pharmacist in drug accountability and temperature maintaining logs. Monitoring Sr. CRC and CRC in maintaining the accountability of study materials and in scheduling study procedures. Endow the required file notes, weekly and monthly and monthly report to the reporting authority. Tracking the status of all study activities. Report to the Site Head daily and take advice for further action. Delegate the work to Senior/Junior/Trainee CRCs as per the requirement.Job Types: Full-time, PermanentSalary: ?10,000.00 - ?15,000.00 per month

Job Description Reviewing and giving medical opinion on various reportsoriginating from literature Reviewing literature references for signal detection andaggregate reports Writing medical comments Contributing to creating search strategiesQualifications Medical University degree (Doctor of medicine) Advanced level of English C1 Good IT skills (MS Office) Good baseline knowledge of scientific literature retrievaland valuation (mainly using PubMed and EMBASE) People who are excited to learn and contribute to patientsafety Excellent organization skills with attention to detail Excellent interpersonal and communication skills

Quality review of ICSRs, surveillance of known or emerging safety issues, participation in an escalation process, risk evaluation, and analysis of safety data. Apply safety concepts and regulations contained within FDA CFR, ICH, and EU GVP to management of Safety data across the development life cycle. Analyze aggregate safety data within a clinical program towards tracking and trending of risk assessments and additional mitigation measures. Contributes to safety sections of the investigational new drug and new drug applications, investigator or regulator communications, Investigator brochure, and other reports (DSUR) Participates in the set-up and maintenance of adverse event processes in global clinical trials Ensure Quality of the Individual Case Safety Report, including data and a concise, medically relevant narrative.

We have vacant of 3 Hospital Pharmacist Jobs in Ramamurthy Nagar Bangalore Experience Required : 1 Year Educational Qualification : Higher Secondary, Diploma Skill Dispensing,Communication Skills,Pharmacovigilance etc.

Department: Medical Communications Content search, writing and editing of several types of documents such as review articles, manuscripts, product monographs, newsletters, case reports, training manuals/slides, CME slide deck, journal summaries, etc Proficient writing and communication skills with flawless English language proficiency, presenting the research data to target audience in a reader friendly manner. In-depth knowledge of various therapeutic areas. Knowledge of relevant guidelines related to structure and contents of specific document with good understanding of Vancouver style of referencing. Familiar with searching medical literature databases such as PubMed, ResearchGate, DeepDive, etc. Perform quality assurance checks on edited manuscripts to ensure that they meet the standards of international publications Provide timely feedback to our editors, manage deadlines, ensure high quality standards and able to furnish primary proofed documents. Delivery of projects/tasks within the given/agreed timelines. Adherence to processes, scientific code of conduct and ethics of writing (reference backed writing and no plagiarism).

Review and execute physicians prescriptions checking their appropriateness and legalityOrganize the pharmacy in an efficient manner to make the identification of products easier and fasterMaintain full control over delivering, stocking and labeling medicine and other products and monitor their condition to prevent expiring or deteriorationListen carefully to customers to interpret their needs and issues and offer information and adviceProvide assistance other medical services such as injections, blood pressure/ temperature measurements etc.Prepare medicine when appropriate using correct dosages and material for each individual patientKeep records of patient history and of all activities regarding heavy medicationKeep abreast of advancements in medicine by attending conferences and seminars and collaborating with other healthcare professionalsComply with all applicable legal rules, regulations and procedures