Full-Time Medical Science Liaison, Gastroenterology/Microbiome (MidAtlantic)
Job Description
- Present healthcare professionals and decision makers with accurate, unbiased, balanced and timely answers to unsolicited request for information about Ferring pharmaceuticals products.
- Establish scientific and clinical relationships with key opinion leaders and academic centers to expand research and educational opportunities for FPI products
- Provide study support from protocol and budget development to submission and completion for Phase IV as well as Investigator Initiated Trials (IIT’s)
- Provide continuing field scientific support and training for sales and Corporate Account Managers (CAM’s)
- Document and forward reports of adverse events to appropriate FPI personnel
- Keep abreast of medical and scientific developments in assigned therapeutic area
- Proactively report competitive activities as well as events that can influence the use of FPI products
- Develop and deliver very specialized scientific/educational programs including but not limited to formulary presentations for managed care and related organizations
- Assist Medical Affairs as well as agency personnel in the development of presentations and slide kits
- Actively participate in advisory boards, speaker training events, clinical investigator meetings, regional national and international meetings when required
- Assist in processing of field request for medical education funding
- Actively participate in key medical and scientific conferences by staffing medical information booths; gathering competitive intelligence on competitors and attending scientific sessions
Qualifications
- Advanced degree (e.g. M.D., Pharm .D. or Ph.D) in pharmacy, medicine, Nursing or a life and or biological science, relevant experience or fellowship is desired.
- The ability to apply technical expertise and solutions to diverse/individualized situations is a must for this candidate.
- Excellent presentation skills as well as the ability to successfully interact with medical professionals at all levels are required.
- Working knowledge of FDA and OIG requirements as well as clinical trial design and statistics is required.
- Work is primarily independent in that it is performed without appreciable day-to-day direction.
- Completed work is reviewed from a relatively long-term perspective for desired results against objectives.
- Represents the organization as a prime field medical contact.
- Willingness to travel 60 % or more of the time
Additional Information
All your information will be kept confidential according to EEO guidelines
How to Apply
Click here to applyhttps://smrtr.io/fDVzR |
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