Sub-InvestigatorDepartment : US Site NetworkLevel : Individual ContributorWork Location : On SiteUpdated Last : 09 / 27 / 2024What We DoCare Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3%. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies.Who We AreWe care. Our people are the engines behind our mission : to revolutionize access to clinical trials for the benefit of patients everywhere. We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations.Position OverviewThe Sub-Investigator will be responsible for regional travel mixed with remote tele-medicine work to support our clinical research. Care Access is looking for Nurse Practitioners or Physicians Assistants to support clinical trial related activities in states throughout the USA.What You'll Be Working OnDuties include but not limited to :Work closely with the Principal Investigator to oversee the execution of study protocols, delegating study related duties to site staff, as appropriate, and ensuring site compliance with study protocols, study-specific laboratory procedures, standards of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), quality (QA / QC) procedures, OSHA guidelines, and other state and local regulations as applicableAttends and participates in meetings with the director, other managers, and staff as necessaryComplies with regulatory requirements, policies, procedures, and standards of practiceRead and understand the informed consent form, protocol, and investigator's brochureBe available to see subjects virtually or in-person as dictated by project design, answer their questions, and resolve medical issues during the study visitSign and ensure that the study documentation for each study visit is completedPerform all study responsibilities in compliance with the IRB approved protocolReview screening documentation and approves subjects for admission to studyReview admission documentation and approves subject for randomizationProvide ongoing assessment of the study subject / patient to identify Adverse EventsEnsure that serious and unexpected adverse events are reported promptly to the PlReview and evaluates all study data and comments to the clinical significance of any out of range resultsPerform physical examinations as part of screening evaluation and active studyConductProvide medical management of adverse events as appropriatePerform other duties as trained for and assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.Physical and Travel RequirementsThis is an on-site position with regional commute requirements. Regularly planned travel within the region will be required as part of the role.What You BringKnowledge, Skills and Abilities :Excellent working knowledge of medical and research terminologyExcellent working knowledge of federal regulations, good clinical practices (GCP)Ability to communicate and work effectively with a diverse team of professionalsStrong organizational skills : Able to prioritize, support, and follow through on assignmentsCommunication Skills : Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients and vendorsTeam Collaboration Skills : Work effectively and collaboratively with other team members to accomplish mutual goals. Bring positive and supportive attitude to achieving these goalsStrong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excelAbility to balance tasks with competing prioritiesCritical thinker and problem solverCuriosity and passion to learn, innovate, able to take thoughtful risks and get things doneFriendly, outgoing personality; maintain a positive attitude under pressureHigh level of self-motivation and energyAbility to work independently in a fast-paced environment with minimal supervisionMust have a client service mentalityCertifications / Licenses, Education, and Experience :Nurse Practitioner or Physician Assistant with 5+ years of clinical experienceCurrently licensed in good standing in one or more states listed aboveA minimum of 1 year of relevant work experience as Sub-Investigator (preferred) in a Clinical Research settingBenefits (US Full-Time Employees Only)PTO / vacation days, sick days, holidays.100% paid medical, dental, and vision Insurance. 75% for dependents.HSA planShort-term disability, long-term disability, and life Insurance.Culture of growth and equality401k retirement planDiversity & InclusionWe serve patients and researchers from diverse cultures and communities around the world. We are stronger and better when we build a team representing the people we aim to support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We value diversity and believe that unique contributions drive our success.At Care Access, every day, we are advancing medical breakthroughs. We're uniting standard patient care with cutting-edge treatments and research. Our work brings life-changing therapies to those in need and paves the way for newer and greater treatments to reach the world. We're proud to advance these breakthroughs and work with the big players while engaging with the bestphysicians and caring for patients. Our team of experts is paving the way to take this vision forward through innovation and a unique technology-enabled.We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
