Job as Medical Research Scientist in Parexel, top level MNC

By: Mitul Shah | Views: 2721 | Date: 07-Jul-2010

Lead training to radiology reviewers for the independent review on the use of software, analysis application, implementation of the review criteria established by the charter, and the applicable securities and regulations.

Over the past 27 years, PAREXEL has developed significant expertise to assist clients in the worldwide pharmaceutical, biotechnology and medical device industries with the development and launch of their products in order to bring safe and effective treatments to the global marketplace for the patients who need them. Headquartered near Boston, Massachusetts, PAREXEL operates in 71 locations throughout 54 countries around the world, and has over 9,500 employees.
We are a leading global bio/pharmaceutical services organization that helps clients expedite time-to-market through our development and launch services. These include a broad range of clinical development capabilities, integrated advanced technologies, regulatory affairs consulting, and commercialization services.
Post: Medical Research Scientist

Job Description:
-Lead training to radiology reviewers for the independent review on the use of software, analysis application, implementation of the review criteria established by the charter, and the applicable securities and regulations.
-Evaluate, as necessary, the results of the independent review and provide necessary guidance or additional training to reviewers.
-Provide imaging technical expertise to project teams conducting clinical trials that rely upon the results of medical imaging studies.
-Assist in developing imaging parameters for specific clinical protocols to ensure standardization of imaging techniques in multi-center trials.
-Act as liaison for the client by providing them technical expertise on medical imaging issues.
-Provide guidance to R&D and application development in the customization of image analysis software tools to meet business needs.
-Coordinate appropriate training activities on relevant imaging topics for staff members, clients, and investigators as necessary.
-Participate in meetings with existing clients and/or presentations to prospective clients, as needed.
-Develop, as necessary, and ensure compliance with relevant standard operating procedures.
-Responsible for quality of deliverables working closely with Process Quality Management staff.
Candidate Profile:
-One year clinical experience or the equivalent, experience with clinical trials, prior consulting experience desirable. Prior experience in a business environment desirable.
-The ability to communicate clearly and precisely, both orally and in writing.
Additional Information:
Experience: 1-2 years
Location: Hyderabad / Secunderabad
Education: M.Pharm, MBBS; MBA
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR, R&D

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