Fellowship - Multidisciplinary (Multiple Positions) Job

The Position The Postdoctoral Multidisciplinary Fellowship is a two-year, experiential program based in Plainsboro, New Jersey. This fellowship is intended to provide an experience for a Doctor of Pharmacy within the pharmaceutical industry. The Fellow will contribute to different functional areas at Novo Nordisk Inc., where a PharmD's training and expertise will provide value to the organization. The Fellow will gain the skills needed to pursue a career within the pharmaceutical industry where their education and experience can make a significant contribution to satisfying customer needs and achieving company goals. During this one-year fellowship, the Fellow will gain experience in three concentrated focus areas: one year in Medical Information and two 6 month rotations, or a 1 year rotation in another functional areas within Novo Nordisk Inc. Relationships The Fellow will report to their Fellowship Manager/preceptor within Medical Information throughout the two-year program and will also have a reporting relationship with a manager in the respective functional areas during their rotations. Additional key internal relationships may include CMR Leadership, Medical Affairs, CMR Training, Clinical Trial Management, and Clinical Development. Essential Functions General Each Fellow will have regular contact with cross functional areas including Regulatory Affairs, Marketing, etc. This structured approach will allow for a broad, "hands-on" experience enabling the Fellows to gain the skills needed to pursue a career within the pharmaceutical industry All Fellows will complete a Fellowship project for presentation at a key conference/congress. Additionally, Fellows may be asked to attend other relevant scientific conventions, national team meetings and othertravel as required for business needs related to fellow projects as appropriate Multidisciplinary Fellows will gain experience for 12months in Medical Information and two additional 6-month rotations, or a 1 year rotation in one of the functional areas listed below Medical Information Gain an understanding of the role and responsibilities of a Medical Information Therapeutic Manager in a pharmaceutical industry setting Develop the skills needed to provide accurate, fair balanced, and current medical and technical information about Novo Nordisk products to healthcare professionals, consumers, managed care organizations and health systems Develop competencies in 1) responding to inquiries in both verbal and written forms, and 2) tailoring the responses to the target audience Update or create standard Medical Information letters and perform literature searches to stay abreast of the latest scientific information in relevant areas Medical Writing (option) Gain an understanding of guidelines for ethical publication practice and reporting of clinical trial data Gain exposure to regulatory writing processes Provide medical writing support to authors in the development of scientific publications and scientific presentations Coordinate internal medical review and author review of publications Assist medical writing members in the preparation of regulatory documents During the development of scientific documents, interact and collaborate with internal and external stakeholders including authors, clinicians, biostatisticians, publication planning group, trial managers, regulatory affairs professionals and medical communications agencies Attend relevant meetings, such as publication planning group meetings, authors' meetings, and project meetings Medical Education (option) Gain an understanding of industry regulations pertaining to independent medical education and ensure that all programs are funded and executed in compliance with these guidelines Participate in the review and evaluation of proposals and grant requests submitted by various medical education companies and accredited providers. Analyze needs assessments, educational objectives and program content in submitted grant requests to ensure alignment with medical education strategy Project manage assigned medical education programs to ensure successful implementation of programs within budget Complete medical accuracy review of live and enduring programs, such as web-based programs, monographs and journal supplements, after their dissemination to intended audiences Product Safety (option) Collaborate with Product Safety case management and functional groups to learn about general pharmacovigilance related activities Gain an understanding of basic FDA/Global Health Authority regulations related to capturing and reporting of safety information Collect verbal and written safety information from physicians, investigators, healthcare professionals, consumers and company sales and field personnel for post-marketing and clinical trial adverse eventreports Perform and prioritize data entry and verification of safety data into the required complaint and safety databases based on internal and external timelines Identify and submit relevant follow-up queries to obtain additional/missing safety information Physical Requirements 10%-15% overnight travel required. Qualifications A Doctor of Pharmacy degree from an Accreditation Council for Pharmacy Education (ACPE)-accredited college of pharmacy with strong academic track record required Demonstrated leadership capabilities Possess good communication skills, both oral, written and presentation Presentable, highly articulate, goal-oriented, honest, with high integrity and strong ethics. Proficiency in PowerPoint, Excel and MS word software applications and overall computer skills with knowledge of literature search techniques required Track record of team work, innovation, and project management Participate in Medical Information projects or task forces Participate in product training for sales representatives and in-house colleagues Be the medical accuracy reviewer as needed for promotional pieces undergoing review by the Promotional Review Board (PR Requisition ID: 58772BR
Salary Range: NA
Minimum Qualification
Not Specified years

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