Clinical Research Study Coordinator

This listing was posted on ApplicantPool.

Clinical Research Study Coordinator

Location:

Portland, OR

Description:

Summary The overarching goal of our research program, Sleep & Health Applied Research Program (SHARP; Co-Directed by: Miranda Lim MD PhD and Jonathan Elliott PhD), is to investigate sleep in neurological conditions including traumatic brain injury (TBI), post-traumatic stress disorder (PTSD), neurodegenerative diseases (e.g., Parkinson's and Alzheimer's Disease), and autism. Preclinical studies in rodents are utilized to translate findings to human subjects, which then further inform and refine rodent studies. We seek highly motivated people who have previous experience with human subjects research, who can work independently and efficiently in a fast-paced and multi-collaborative environment. This position is for a Clinical Research Coordinator to coordinate and conduct study visits for the SHARP clinical research program ( https://sharp.pvarf.com/ ) under minimal supervision. The Research Coordinator will complete study visits for multiple research studies and also assist with research in clinical space, as permitted. This position requires on-site work with occasional opportunities for telework after the initial onboarding and training period. If applying from outside Portland, OR please indicate in cover letter concrete plans or indicate an intention to relocate to the Portland metro area. Applications that do not address this will not be considered. Salary will be commensurate with experience in clinical practice, clinical research, and education relevant to our clinical research studies. ESSENTIAL DUTIES AND RESPONSIBILITIES Serve as study coordinator on multiple clinical research projects with minimal supervision. Takes initiative to lead portions of studies and coordinate work for a multidisciplinary research team. Ability to stay highly organized with electronic management of large datasets and assist with administrative tasks as needed. Complete study and/or clinic visits for multiple research studies. Recruit, screen, and consent participants. Ability to communicate with lab members regularly and contribute in a positive manner to team dynamic. Ability to work under pressure and with time constraints JOB DUTIES Plan & conduct human research studies including participant recruitment and retention. Manage several aspects of the SHARP clinical research program with minimal supervision. Data entry into shared database and data management. Maintain local site documentation and records, adhering to all regulatory requirements. Process and analyze data from human subjects Respond to general inquiries from study participants and clinical staff. Attend regular clinical and/or research team meetings. Prepare research projects for Institutional Review Board (IRB) submission and review process Contribute to abstracts, manuscripts, and presentations as needed. Ability to work onsite with phone and video conferences as occasional teleworking may require. Train and oversee other personnel in the above techniques as needed QUALIFICATIONS Ability to perform essential job duties with or without reasonable accommodation and without posing a direct threat to safety or health of employee or others. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE Bachelor's degree in health relevant field required, graduate degree or advanced training relevant to clinical research or clinical care preferred 3+ years direct patient care or clinical research experience Experience working with vulnerable patient populations preferred COMPUTER SKILLS Advanced skills in Microsoft Word, Excel, PowerPoint preferred Skillfully uses a PC as primary means of communication (email, video conferencing, Slack) Facile with troubleshooting and maximizing internet connectivity Able to troubleshoot new computer software as needed for data collection and analysis Experience with database management a plus LOCATION and ADDITIONAL INFORMATION Primary job location is located on the VA Portland Health Care System campus. New employees must submit COVID-19 vaccination documentation or seek an exemption within 8 weeks of beginning employment. The Portland VA Research Foundation is an equal opportunity, affirmative action organization. All qualified applicants will receive consideration for employment without regard to status as a protected veteran or a qualified individual with a disability, or other protected status such as race, color, sex, sexual orientation, gender identity, religion, national origin, or age. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. Please apply online at http://www.pvarf.org and include a CV and cover letter explaining your interest in the position. Cover letter should include description of recent work history as it relates to the specific responsibilities in the job announcement. Job Posted by ApplicantPro

Company:

Portland Va Research Foundation

Posted:

December 26 2023 on ApplicantPool

Visit Our Partner Website

This listing was posted on another website. Click here to open: Go to ApplicantPool

Important Safety Tips

Always meet the employer in person.
Avoid sharing sensitive personal and financial information.
Avoid employment offers that require a deposit or investment.

To learn more, visit the Safety Center or click here to report this listing.

Clinical Research Study Coordinator | Clinical Coordinator in Nurse & Healthcare Job at Portla1

Clinical Research Study Coordinator

Visit Our Partner Website