Clinical Assistant Job Vacancies in Gujarat

We are looking for a dedicated Clinic Assistant to join our team in Ahmedabad. This part-time role is perfect for a female candidate with up to 3 years of experience or fresh graduates.**Key Responsibilities:**- **Patient Greeting and Check-in:** Welcome patients as they arrive at the clinic and assist them with the check-in process to ensure a smooth experience. - **Appointment Scheduling:** Manage and coordinate patient appointments, ensuring efficient use of scheduling systems and minimizing wait times. - **Medical Record Management:** Assist in maintaining and organizing patient medical records, ensuring information is accurate and confidential. - **Communication with Patients:** Provide clear information to patients regarding their appointments, treatments, and any necessary follow-up procedures. - **Basic Administrative Tasks:** Perform general office duties, such as answering phone calls, responding to inquiries, and keeping the waiting area organized. - **Assisting Healthcare Staff:** Support doctors and nursing staff with various tasks, like preparing examination rooms or gathering necessary supplies for patient care. **Required Skills and Expectations:**Ideal candidates should have a high school diploma and strong communication skills to interact effectively with patients and staff. A friendly demeanor is essential, along with the ability to handle multiple tasks efficiently in a fast-paced environment. Basic knowledge of clinic operations or experience in a healthcare setting is a plus but not mandatory. A commitment to patient care and maintaining confidentiality is crucial in this role.

I Required Nursing Staff Who Manage Clinic and Assist Doctor,Good Behavior,And Know English and Some About Experience About Clinic Work

Looking For The Profile Of Junior/Assistant Sales Manager For One Of A Leading Skin Clinic In Surat

Ensuring your learning curve is high at all times Ensuring that customer service is top of the game and as per our standards Consulting prescriptions and patients Arranging the medicines in the racks and in medical boxes Recommending another brand of medicine but of the same molecule to the patient Answering Customer queries face to face or by Phone Selling OTC medicines and various offers Managing of expiry medication Billing process in computer software Handling cash in billing counter and deposit in the bank Monitoring and analyzing the expenditure on drugs, providing reports as required Conducting accurate weekly audit process Establishing, developing and maintaining relationship with existing and new customers

Candidate will help in clinic as per given instructions.

1) Identify new sites. PIs and conduct the detailed protocol specific feasibility.2) Preparation for site selection visit3) IRB submission & approval4) Regulatory document collection5) Set-up. maintain & timely update or Trial Master File(TMF) & relevant site binders Files6) Prepare site for Site Initiation Visit (SIV)7) Assisting Principal Investigator in administering the Informed Consent Form process8) Ensure protocol adherence and Compliance; t document protocol deviations as appropriate and communicate any impacting subject safety to !he Ethics Committee. 9) Pre-screening, screening, enrolling & recruiting subjects.10) Creating and Preparing Source Documents and their templates11) Coordinate and schedule subject's regular follow-up Visit and Procedures. preventing lost to follow-up & missed visits. Maintaining regular contact With Subject Telephonically12) Manage Clinical Trial Materials (CTM ). accountability, distribution & logistics at site13) Filling the case reports forms and Electronic case report forms and resolving all data queries within timelines.14) Reporting and coordinating all Adverse Events & Serious Adverse Events according to their timelines.15) Filling up and maintaining trial related logs like drug dispensing logs, subject logs. investigational Product t Logs, temperature logs. Etc. 16) Maintaining Calibration records of Instrument used for the trials.17) Preparing Site for monitoring & audit visits. Coordinate close out visit & archival at site.18) Communicating all protocol-related issues problems to the appropriate management staff including but not limited to questions regarding the conduct of clinical trials. Concerns regarding possible serious adverse events or subject compliance.19) Co ordinate central lab logistics & sample flow. Review lab data & communicate abnormal values to the primary care provider(if appropriate) & investigator.20) Co ordinate subject reimbursements.21) Performing all the above activities i