Number of workers: 350
Veeda Clinical Research® is a full service global CRO specializing in the early clinical development of drugs. With state-of-the-art facilities in India, the US, Malaysia and Belgium, we provide a full range of services in phase I and IIa clinical research, delivering expert, cost effective research solutions to the Pharmaceutical and Biotechnology Industries worldwide.
Veeda CR has been inspected by the FDA, MHRA and WHO and is DCGI and ANVISA approved, as well as winner of Frost and Sullivan’s “Indian Clinical Research Organization of the Year 2009” and Frost and Sullivan’s “Partner of Choice” for phase I studies in 2007.
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> Answering a multi-line telephone >Guest Management > Guest House Management >All Coordination on mail > Handel Stationery Record & Order > Driver & Trip Management > Coordinating with MD / HOD / Clients for all work > Filing all invoices & Data Management > Coordination for vendor payment & bills. > Ticket Booking & Hotel Booking > Handel Petty Cash > Scanning / faxing > Handel Central Housing Office and procedures. > All kind of general ...Last update: 6 days ago
Recruitment: 1.Sourcing of suitable profiles related to Openings from the diff sources like Job portal , Old database , References 2.Assist the recruitment by way of coordinating the interviews/ preparing offer letters of the selected employees. 3.Recruitment Database Management which include management of CVs Pre/ Post- Interview activities Time Keeping: 1.Daily tracking of attendance and updating the ...Last update: 8 days ago
Job Responsibilities A. Travel Desk 1. Organise Domestic Travel and Documentation for HOD’s ,Directors and Unit heads 2. Organise International Travel and Documentation for Veeda staff, HOD’s, Directors and Unit heads 3. Organise complete travel services for GMD. 4. Ensure fast Visa Processing/documentation works 5. Responsible for other travel related services like national and international Hotel ...Last update: 8 days ago
CRA – Freelancer Task As Monitor: - 1. Study Site Qualification / Initiation / Monitoring / Close-out visit for the sites in the city and in the nearby location accessible by an overnight journey (not more than 10 hours) a. Shall plan the visit as per the SOP for Site qualification / initiation / monitoring / close-out b. To perform the visit as per the requirement of the project and in accordance to the SOP for Site ...Last update: 57 days ago
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- Veeda Clinical Research