Junior Accountant ODH DEVELOPERS PRIVATE LIMITED

14.0 - 24.0 years

0 - 0 Lacs

bangalore, iran, singapore

On-site

We are looking for an ambitious Junior Accountant to provide support to the financial department by managing daily accounting tasks. You will be part of a team of professionals working to maintain order and transparency for the companys finances. Preparing financial statements and reporting are a large part of the junior accountants day-to-day work. The ideal candidate will be well-versed in accounting principles and able to work comfortably with numbers and attention to detail. The goal is to contribute to the overall efficient operation of the department and help the company be fully aware of its financial condition. This way it can make the right decisions and accomplish long term success. Responsibilities Post and process journal entries to ensure all business transactions are recorded Update accounts receivable and issue invoices Update accounts payable and perform reconciliations Assist in the processing of balance sheets, income statements and other financial statements according to legal and company accounting and financial guidelines Assist with reviewing of expenses, payroll records etc. as assigned Update financial data in databases to ensure that information will be accurate and immediately available when needed Prepare and submit weekly/monthly reports Assist senior accountants in the preparation of monthly/yearly closings Assist with other accounting projects

Posted 12 hours ago

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Clinical Research Associate RIANSHI DEVELOPERS PRIVATE LIMITED

1.0 - 5.0 years

0 - 0 Lacs

bangalore, dharwad, bilaspur

On-site

A Clinical Research Associate (CRA) plays a crucial role in clinical trials, ensuring they are conducted ethically and in accordance with regulations. CRAs monitor trials, manage data, and ensure participant safety . They act as a key liaison between sponsors, research sites, and other stakeholders. Key Responsibilities: Monitoring Clinical Trials: CRAs conduct site visits to verify that trials are following the study protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. Data Management: They oversee the collection, documentation, and entry of data into electronic data capture (EDC) systems, ensuring accuracy and completeness. Participant Safety: CRAs are responsible for ensuring the safety and well-being of trial participants. Regulatory Compliance: They ensure that trials adhere to all relevant regulations and guidelines, including those from regulatory bodies like the FDA. Communication and Liaison: CRAs serve as a primary point of contact between the sponsor, investigators, and other stakeholders, facilitating communication and resolving issues. Site Management: They may be involved in identifying and qualifying potential investigators, setting up research sites, and managing study supplies. Report Preparation: CRAs contribute to the preparation of reports, including interim monitoring reports, and may be involved in the development of publications based on trial data. In essence, a CRA is responsible for the operational aspects of clinical trials, ensuring data integrity, participant safety, and regulatory compliance

Posted 1 day ago

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