A medical device research organization needs applicants for an opening for a Telecommute Quality Systems Principal Medical Research Manager. Core Responsibilities of this position include: Acting as a lead during ISO audits and FDA inspections.
10+ years of relevant experience. Strong track record of performance on cross-functional teams. Extensive knowledge and experience in drug development, medical, and/or commercial disciplines. Strong leadership, negotiation, interpersonal, communication, and meeting facilitation skills.
A staffing agency is seeking a Telecommute Senior Medical Writer in Morrisville. Must be able to: Provide high-quality medical and scientific writing from planning and coordination of literature search. Manage all aspects of planning, organizing, and executing projects.
Creating and executing medical education programs. Working on logistics, content management and client submissions. Working closely with client and internal agency teams. Qualifications for this position include: Ability to travel to programs and work-from-home Fridays.
, D. O. , or Ph. D. Experience teaching allopathic or osteopathic medical students in clinical sciences. 5 years experience writing “board-style” assessment items. Proficiency in Microsoft Office and Google products. Must demonstrate the ability to edit and write clearly and concisely.
Designing and implementing total care model to source medical and PD data. Leading and coordinating utilization and pricing analysis that ensures appropriate claims on contracts. Position Requirements Include:
A medical devices company is filling a position for a Telecommute Lead Clinical Research Associate. Core Responsibilities Include: Participating in multiple internal cross functional teams. Participating in project team meetings. Electing qualified and experienced research sites.
Must meet the following requirements for consideration: Approximately 20% travel. 9+ years of experience. Bachelor's degree in science or engineering required. Working knowledge of appropriate global medical device regulations, requirements, and standards.
Experience in Clinical Data Management practices and relational database management software systems. Knowledge of medical terminology, clinical data, and ICH/Good Clinical Practices. Proficiency in MS Windows navigation, Word, Excel, PowerPoint, and email applications.
Qualifications Include: MA or MS in statistics subject, preferably with a strong medical statistics component. 8 years of postgraduate experience in the application of statistics to clinical trials for employees with an MA/MS in statistics subject.