Prime Square Building, Plot No 1,
Gaiwadi Industrial Estate, S.V. Road, Goregaon (W)
Mumbai : 400062
Company Profile
Super Religare Laboratories Ltd is a Ranbaxy promoter company in the business of Medical Diagnostics and Crinical Research. Super Religare Laboratories Ltd is India's first & foremost Clinical Trial Central Lab meeting all International Standards and Accreditation having presence in South East. We started a revolution in diagnostic services in India, by ushering in the most Specialized Technologies with Innovative Services. The phenomenal response from the medical profession has helped Super Religare Laboratories Ltd to grow into a leader in Indian & International Diagnostic Laboratory Services thereby catalysing the expansion process.
Super Religare Laboratories Ltd has the largest Pathology Laboratory Network all over India offering more that 3000 tests and over 95 Technologies, supported by full integrated Lab management system. We have Super Special Specialized Laboratories located in major Indian cities. Our Sales Operations extend over 350 cities with the support of 550 sample collection centers spread across India.
With ethical standards and customer care as our core values, we provide accurate solutions for preventive and wellness health. Our 800+ strong workforce and part of the exponential growth plans. We invite bright professionals who believe in Quality and Excellence and have aspirations to grow in our fast paced organization.
Date Management Officer
Experience: 1 - 2 YearsLocation: Mumbai
Education:UG - B.Sc - Any SpecializationPG - M.Sc - Bio-Chemistry, Biology, Chemistry, Computers, MicrobiologyRole: Clinical Researcher
Job Description
DATABASE SET UPAs per defined internal time frames taking into consideration the sponsors time frame for initiation of the study.1. Ensure Database set up in accordance with the study protocol, Electronic Data Transfer specifications, sponsor time frame for each contracted study and in compliance with all SOPs pertinent to the data set up process.2. Following the time lines provided by the DME and the sponsor for completion of the database set up prior to FPFV at SRL.3. Building of the test SOPs in the database prior to study initiation.4. Update of Recipe cost for each new test SOP/Code built in the LIS system. Ensuring the set up of Study Masters to include the Study related details pertaining to the protocols.5. Co-ordinating with the IT team and the Lab sections in case if there are issues with the Instrument Interfacing for the CRS Accessions.6. Ensure 100% compliance with all SOPs pertinent to the data setup process without any deviations.DATA MANAGEMENT - PRODUCTION PHASEOngoing for each study1. 100% implementaion of all relevant SOPs & processes related to the production phase of the assigned studies & thereby ensuring 100% sponsor satisfaction & 0% data management related issues.2. Completing all daily tasks assigned by the DME, maintaining all study documentation/Files on a real time basis.3. Initiating weekly co-ordination with the sponsors data management and IT team and taking necessary actions on the inputs received.4. Follow up for all the pending tasks and activities.5. 100% implementation of all the SOPs to ensure no deviations
Desired Candidate Profile
ADDRESSING QUERIESOngoing for each studyInterfacing with the Assigned Project team and the IT department in resolving queries raised by the sponsor on real time basisAddressing of Critical Issues & unanswered queries in liasion with the internal departmentsTEAM SUPPORTOngoingSupport the DME, fellow team members and CRS OM for the smooth execution of the Project & to build a strong CRS team.Proactively assisting the fellow team members & DME for the smooth execution of the Project
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