Clinical Results and Medical Consult Sub-Investigator

Posted 4 months agoViewed
United StatesFull-TimeHealthcare
Company:Care Access
Location:United States
Languages:English
Seniority level:Senior, 2 years
Experience:2 years
Skills:
DocumentationCommunication SkillsCollaborationProblem SolvingAttention to detailComplianceCritical thinkingResearch
Requirements:
Minimum of 2 years of clinical experience as APP Clinical research experience preferred Telehealth experience preferred Active unrestricted NP or PA license Multi-state licensure required Excellent communication and patient interaction skills Strong attention to detail and ability to manage multiple patients efficiently Ability to work independently while collaborating with a larger clinical team Excellent working knowledge of medical and research terminology Excellent working knowledge of federal regulations, good clinical practices (GCP) Ability to communicate and work effectively with a diverse team of professionals Strong organizational skills Strong verbal and written communication skills Team Collaboration Skills Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel Ability to balance tasks with competing priorities Critical thinker and problem solver Curiosity and passion to learn, innovate, able to take thoughtful risks and get things done Friendly, outgoing personality; maintain a positive attitude under pressure High level of self-motivation and energy Ability to work independently in a fast-paced environment with minimal supervision Must have a client service mentality Willingness to maintain and obtain additional state licenses as needed.
Responsibilities:
Receive and review flagged abnormal, urgent, or critical test results. Contact patients to communicate abnormal test results and provide medical consults. Address and triage test-related or medical escalations from other teams. Oversee execution of study protocols and delegate duties to site staff. Ensure site compliance with study protocols, GCP, SOPs, and regulations. Review informed consent forms, protocols, and investigator's brochures. Be available to see subjects, answer questions, and resolve medical issues. Sign and ensure completion of study documentation for each study visit. Perform physical examinations as part of screening and study conduct. Provide medical management of adverse events. Accurately document all communications in patient progress notes.
About the Company
Care Access
View Company Profile
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