Sr. Clinical Research - Project Manager
Title: Sr. Clinical Research? Project Manager --?Health care Software?
Location:?? Florida?
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Position / Company Description:
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Our exclusive client, a Health care/Software Company, is rapidly transforming itself from a young, aggressive start up to one of the fastest-growing and most respected companies in the industry. It is a company full of visionaries with a fierce entrepreneurial spirit. This is a global firm with health care software? installed in several prestigious accounts in the pharma-life sciences industry.??
?Its innovative products have helped speed the process of taking life-impacting treatments from inspiration to reality.?
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Due to recent expansion they are seeking a qualified clinical research ?project manager who will interface with customers in the use of their health care software product.? This is a tremendous opportunity for career growth and challenge at a proven and successful company.
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?For individuals who have clinical research, CRA, clinical trials experience, OR ?project management in clinical trials or research?all with?customer service and are committed to excellence,?this position is for you!?
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The Key Objectives are:
??????????? Serve as the post sales key client contact and ensure that the project is kept on time and on budget
??????????? Learn our client's health care Software product and the processes they utilize for clinical studies
??????????? Train clients in use of health care software for use in clinical trials,?using Web Ex with heavy on site training
??????????? Work with clients, such as Medical Device, CRO's, Pharma and Biotech firms?
??????????? Develop strong and effective customer relationships
??????????? Provide excellent customer service that answers client questions on a timely basis, resolves problems, and produces high customer satisfaction
??????????? Maintain oversight of project process and act as a project team lead for assigned accounts
??????????? Track and communicate project status to Vice President
??????????? Ensure that project deadlines are met
Candidate Requirements:?
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Must have:?
????? A minimum of?2-3 years project management experience preferred from the Pharma, Biotech, CRO within Clinical Trials
????? One Year Data Management Experience
????? Exceptional attention to detail and the ability to produce accurate specifications for complete software implementation
????? An analytical and detail-oriented thinker
????? Communicate well both verbally and in writing with demonstrated ability to be pro active and develop strong customer relationships
????? Must have good public speaking abilities in front of a large group
????? Know how to train people effectively in clinical trials
????? Strong organizational and follow-up skills
????? Solid understanding of computer systems, clinical trail technology terms and the ability to demonstrate products using Web Ex
????? Self motivated, be able to work independently with little supervision
????? Have the ability to learn new processes and procedures quickly
????? Willingness to travel?about 10% of the time
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???????? ?????? Prefer:
????? Prior E/CLINICAL, DATA Management OR SAFETY SOFTWARE Technology?EXP.
????? Certificate with CRA : 2-3 Years as a CRA
????? Degrees: B.S., Bus. Or L.S.
????? LPN
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Compensation:
Compensation commensurate with track record and experience and stock options
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Keywords Relevant to this Position:
clinical research or clinical trials,?? project manager, customer service or client service, CRA or clinical research associate, EDC or electronic data capture, eclinical, data management, Phase forward, Medidata, pharma, biotechnology, sfbc, eTrails, CRO, PRA, Parexel, Perceptive Informatics, PRA, PPD, Quintiles, Covance?
Skills/Qualifications:
GCP, Trial Development, Planning, Quality Management, Supervision, Reporting Skills, Trial Development, Clinical Lab Testing, Lab Environment, Research Skills, Scientific Curiosity, Strategic Planning, Process Improvement, Analyzing Information, Verbal Communication, Clinical Research, investigators, pre-trial site visits, training, monitoring trial drug accountability; clinical requirements;
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Contact Information:
Please send your resume as a MSWord attachment
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DUE TO THE VOLUME OF RESPONSES, WE CANNOT RESPOND TO ALL APPLICATIONS.? THEREFORE, IF YOU DO NOT MEET THE SPECIFIC QUALIFICATIONS LISTED, WE WILL BE UNABLE TO RESPOND TO YOUR RESUME.? ONLY QUALIFIED CANDIDATES WILL RECEIVE A RESPONSE.? THANK YOU FOR YOUR COOPERATION.
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Biotechnology and Pharmaceutical 
