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Montana Medical Research

Are you seeking employment where you make a difference and be challenged? A job that has potential for growth, where you can continue to learn new ideas? Consider a job in Clinical Research. Montana Medical Research has an opening for a Research Assistant. The Research Assistant is an essential member on the Clinical Research Team.Duties include:<ul><li>collecting clinical tests such as ecg, vitals, spirometry</li><li>Assist in the recruitment of prospective research patients</li><li>Maintain clear and precise records</li><li>Conducts prescreening interviews</li><li>Enters data into study database</li><li>Assists the Clinical Research Coordinator and Investigator in the conduct of clinical trials.</li><li>Maintains confidentiality of sensitive information</li><li>Greets and provides assistance to visitors and patients in a professional manner</li><li>Answers phone and directs calls to the appropriate person</li></ul>The above duties are not meant to be a comprehensive list, but a guide to general job duties of the position.Qualified applicants should be:<ul><li>Well Organized</li><li>Familiar with Microsoft Office</li><li>Possess superior communication skills</li><li>able to work independently as well as part of a team</li><li>experience with medical terminology.</li><li>attention to detail</li><li>ability to multi-task</li></ul>Job Types: Full-time, Part-timePay: From $18.00 per hourBenefits:<ul><li>Health insurance</li><li>Paid time off</li><li>Retirement plan</li></ul>Work Location: In person

Research Assistant/ Medical Assistant

Are you seeking employment where you make a difference and be challenged? A job that has potential for growth, where you can continue to learn new ideas? Consider a job in Clinical Research. Montana Medical Research, Inc has openings for a Clinical Research Coordinator.Job descriptionFull Job DescriptionThe Research Coordinator is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.Essential Responsibilities and Duties:<ul><li>Primary responsibility is to screen, enroll and follow study subjects ensuring protocol compliance and monitoring while the subjects are on study</li><li>Responsible for all data collection, source documentation, completing study specific case report forms, and submission of adverse experience reports</li><li>Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, subject logs and study-related communications</li><li>Schedule subjects in protocol defined windows</li><li>Go through the consent form with patients and ensure that they understand and sign ICF prior to any study related procedures.</li><li>Perform ratings scales that you have been trained on</li><li>Communicate with sponsors and CROs and reviews and responds to any monitoring findings and escalates issues</li><li>Make IRB submissions in collaboration with the regulatory coordinator (Continuing reviews, SAEs, protocol deviations, and other when required) and maintain IRB binder</li><li>Resolve queries in a timely manner and be capable of entering data into the EDC if assistant is not available to do so</li><li>Communicate with PI regarding trial requirements, safety evaluations, regulatory, and monitoring</li><li>Ensure that the PI signs off on labs, AEs, and ECGs in a timely manner</li><li>Ensure all regulatory binders are up to date</li><li>Recruit patients via research database, ad campaigns, and MD-MD letters</li><li>Phlebotomy and ECGs</li><li>Understand disease states</li><li>Dispense IP and perform accountability</li><li>Communicate with vendors</li><li>Communicate with patients and caregivers</li></ul>Qualifications<ul><li>Bachelors degree in a life science or At least 2 years of relevant work-related experience in the medical field</li><li>CCRC certification not required, but preferred</li><li>Knowledge of &ldquo;good clinical practices&rdquo; for clinical research as defined by the Code of Federal Regulations (CFR). Preferred but not required</li><li>Demonstrate organizational skills to efficiently and effectively manage multiple clinical trials while providing accurate information in a timely manner.</li><li>Communicate and work effectively with a diverse team of professionals</li><li>Phlebotomy and ECGs experience not required, but preferred</li><li>Demonstrated interpersonal skills to work with physicians, administrators, work colleagues, representatives from sponsors and others to achieve maximum efficiency in reaching and maintaining workplace goals in a professional manner.</li><li>Must be self-directed and be able to manage multiple projects and responsibilities.</li><li>A critical thinker with strong attention to detail and superb problem-solving abilities.</li><li>currently reside in geographical location or have housing arranged</li></ul>Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.Job Type: Full-timeBenefits:<ul><li>Retirement</li><li>Employee assistance program</li><li>Health insurance</li><li>Paid time off</li></ul>Job Type: Full-timeJob Type: Full-timePay: $20.00 - $28.40 per hourBenefits:<ul><li>401(k)</li><li>Flexible schedule</li><li>Health insurance</li><li>Paid time off</li></ul>Work Location: In person

Clinical Research Coordinator

Join Montana Medical Research and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Montana Medical Research

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Research Assistant/ Medical Assistant

Clinical Research Coordinator