Drug Safety Job Vacancies in Chennai

As a Pharmacist at Lotus Polyclinic, you will:- Dispense prescribed medications accurately and safely- Counsel patients on dosage, side effects, and drug interactions- Maintain pharmacy inventory, stock levels, and expiry management- Coordinate with doctors and clinical staff regarding prescriptions- Ensure compliance with Drug Control and Pharmacy Council regulations- Manage billing, records, and pharmacy documentation- Provide OTC medication guidance and basic health advice- Maintain hygiene, storage standards, and cold-chain protocols- Support patient-centric service and ethical pharmacy practiceRequirements:- B.Pharm / D.Pharm with valid Pharmacy Council Registration- Minimum 1 year experience in retail or hospital pharmacy (freshers may apply)- Strong knowledge of prescription handling and drug safety- Good communication skills in Tamil & English- Basic computer and billing software knowledge- Ability to work in shifts and weekends- Professional attitude and patient-care mindsetPreferred Skills:- Experience with clinic or hospital pharmacy setup- Knowledge of inventory management systems- Familiarity with generic medicines and brand alternatives- Customer service & counselling skills- Immediate joiners preferredWhy Join Lotus Polyclinic?- Friendly and ethical work environment- Career growth in a multi-specialty clinic- Competitive salary + incentives- Learning exposure with doctors and specialists- Stable, long-term opportunity

Collections Specialists are generally responsible for managing and collection all the outstanding accounts receivables form clients and customers. In addition, they may be responsible for other aspects of collections, resolve customer billing problems and reducing the amount of accounts receivables.

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