A medical product manufacturer has a current position open for a Telecommute Clinical Research Associate in Newport News. Core Responsibilities Include: Handling studies involving chronic wound care. Improving clinical outcomes. Any other requirements set forth by the employer.
A medical device company has an open position for a Remote Medical Device Partnership Enablement Associate Director. Candidates will be responsible for the following: Creating training programs for cross-functional study teams and governance members.
Position Requirements Include: High school diploma or GED or higher. 1 years of customer service experience in a Medical insurance position, and knowledge of medical/insurance terminology. Intermediate proficiency with MS Word create, copy, pastes.
Medical and Health Sciences. Cardiology & Hematology. Clinical Medicine - all disciplines. Dentistry. Emergency Medicine. Forensic Sciences. Medical Technology. Metabolism / Diabetes. Neuroscience / Neuroanatomy / Neurosurgery. Ophthalmology. Optometry. Orthopaedics.
Skills and Requirements Include: 25% travel. BA/BS required. 4+ years of research and leadership experience or combination of education and experience. Familiarity with medical terminology. Strong proficiency in Microsoft Office Programs. Ability to type proficiently (35+ wpm)
Intermediate proficiency in performing data analytics. 3 years of work experience in a corporate setting. Bachelor's degree or equivalent work experience. 1 years of health care experience working with claims data and medical codes.
5 years of medical writing experience in a pharmaceutical company. 5 years of experience in a medical writing role, including participation in submissions to the US FDA. Demonstrated experience in the preparation of protocols, study reports, investigator brochures.
Minimum of 4 years of medical writing experience in a pharmaceutical company. At least 4 years of experience in a medical writing role, including participation in submissions to the US FDA. Demonstrated experience in the preparation of protocols, study reports, investigator brochures.
Excellent analytical skills, with the ability to process scientific and medical data. Expertise in manipulating and analyzing SAS data. Ability to identify data issues, present problems, and implement solutions. Familiarity with clinical trial design and analysis activities.
Leading the ongoing medical /scientific review of the clinical trial data. Authoring Clinical Study Protocol, amendments and related documents. Contributing to the evaluation of clinical sites and external service providers. Qualifications Include: Interacting with investigator sites.