Clinical Trial Specialist- Novartis

Job Summary Company Name Novartis Healthcare Private Limited Locations Hyderabad Experience 0 - 2 years Keywords / Skills TBD, "Clinical Research Specialist", "Drug Supplies", "Clinical Documents" Function Pharmaceutical/ Biotechnology Role Clinical Research Scientist Industry Pharmaceuticals Posted On 25th Apr 2013 Job Ref code APPLY  Rate this job

Novartis Healthcare Private Limited Job DescriptionApply via below link: http://jobs.monsterindia.com/details/13256944.html?sig=js-1-d3928b0aa22ff2e12cd6c4f8861fced4-1&from= Job Purpose: Support the clinical trial team (CTT) in the administrative coordination of trial activities through specific tasks, including but not limited to budget, document management, drug supply, trial master file, and archiving, preparation of selected clinical study report (CSR) appendices, and provide overall support to the CTMR department, as assigned. Major Accountabilities: 1. Budget responsibilities: a.  Track, verify, and reconcile vendor invoices with actual work performed for payment 2. Document management: a. Coordinate and maintain records to track flow of life cycle management in the document management system for appropriate assigned document (i.e., Vendor Activity Worksheet). Ensure the business process for review and approval of documents is adhered to. 3.       Drug Supplies:  a.       Collect and verify the drug batch information received per patient for CSR appendix documentation for trials without IVR tracking b.       Verify at the global level for re-supply needs for all study drugs at the CPOs for trials without IVR tracking 4.       Tracking and archiving: a.       Responsible to set up and maintain HQ Trial Master Files (TMF) and ensure files are complete for each study center according to Novartis SOPs and guidelines. b.       Track IRB/EC approvals dates and addresses for protocols and amendments c.       Using the Novartis tracking tool, track receipt of documents from the field and verify completeness of documents for HQ TMF (e.g., tracking of FDA form 1572, financial disclosures, and CVs for CSR appendices) d.       Interact with clinical team members, field monitors, and other study team personnel to resolve issues with missing, incomplete, misfiled documents e.       Support archiving of required trial information (i.e., investigator meeting presentations, study correspondence) and posting of study documents (ensuring correct format and naming con-ventions) as directed by the clinical team 5.       Clinical Documents: a.       Responsible for FPP process b.       Support the appendices preparation for the CSR completion c.       Verify that study documents (i.e., protocols, amendments, TOOs and CSR appendices) are correctly filed in CREDI; support completion of submission eTMF tracker d.       Ensure correct eCTD file naming convention for reference finalization in document manage-ment systems (e.g. CREDI ) e.       Insert active hyperlinks within Regulatory documents, QC of hyperlinks in clinical documents to ensure accuracy f.       Interface with document publishers on behalf of clinical teams to ensure availability of ‘pub-lished’ quality documents that are delivered according to timelines and technical specifica-tions. g.       Support collection of published scientific references and import into CREDI ensuring correct format and naming conventions in support of the preparation of various clinical submission documents (e.g., expert statements, clinical overview, Annual Safety Report) 6.       Other duties and responsibilities as assigned a.       Maintain CTMR Sharepoint as appropriate (e.g., correct content and links) 7.       Trouble shoots problems and is a liaison between the CTMR and CREDI help desk Key Performance Indicators: TBD Ideal Background  Education An advanced (Masters) degree or equivalent qualification or work experience is required 0-2 years Languages:                           Experience: -         Excellent word processing skills with advanced MS Word are required -         Proven experience working with computers -         Experience working with the documentation system -         Strong intrapersonal skills, customer focused, and ability to work independently managing multiple priorities across a global organization -         Well-organized, detail-oriented and excellent follow-up skills -         Good oral and written communication skills are required -         Working knowledge of the various types of clinical documents is helpful -         Basic understanding of the clinical drug development process, Good Clinical Practice and familiarity with medical terminologies is a plus -         English (oral and written)

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