Fresher 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

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

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

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

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