Jamie Steed Email and Phone Number
As a clinical research professional, I have 7 years of experience in providing research support, coordination, and leadership for Phase II and III clinical trials sponsored by NIH, investigators, and industry. I am skilled in handling multiple projects with high accuracy and success rates. I am proficient in using various technical applications, data, and project management systems such as Microsoft Office tools (Word, Excel, PowerPoint), Microsoft 365, One Drive, SharePoint, DropBox, Outlook, Trello, EPIC, Qualtrics, and research management platforms including ERT, EDC, IMedidata, IRT, Site Vault, REDCap, and Medavante. I have prior clinical experience of 8 years working in healthcare with multiple patient populations. I specialize in behavioral health, oncology research, health disparities research, and community-based participatory research. Additionally, I have expertise in qualified behavioral assessment questionnaires. My goal is to inform, educate, and empower our communities about clinical trial research and the detrimental effects of postpartum depression on maternal and infant health. Throughout my career, I have been involved in several clinical trials to evaluate the safety and efficacy of various treatments for postpartum depression in women. These include personalized integrated chronotherapy, Zuranolone, and SAGE 547 (FDA-approved Zulresso). The clinical trials that I have worked on are:1. Personalized Integrated Chronotherapy for Perinatal Depression: PI- Dr. Samantha Meltzer-Brody November 2020-present2. Depression, Aging Stress, and Heart Health Study (DASHH): PI- Dr. Margo Nathan, November 2022-present3. Skylark Study (SAGE-217-PPD-301), Phase 3: PI- Dr. Meltzer-Brody February 2021-May 20224. Robin Study (SAGE-217-PPD-201), Phase 2: PI- Dr. Meltzer-Brody, March 2018-March 20195. Chickadee Study (SAGE-547-PPD-304), Phase 3: PI- Dr. Meltzer-Brody, January 2020-May 20216. Hummingbird Study (SAGE-547-202B and 202C), Phase 3: PI- Dr. Meltzer-Brody, June 2017-September 2017The purpose of these clinical trials is to improve the health and well-being of women suffering from postpartum depression.It has been a miraculous journey to be a major part of such innovative research and to witness life-changing treatments become accessible to many women suffering from postpartum depression.
University Of North Carolina At Chapel Hill School Of Medicine
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Clinical Research SpecialistUniversity Of North Carolina At Chapel Hill School Of MedicineChapel Hill, Nc, Us
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Clinical Research SpecialistUniversity Of North Carolina At Chapel Hill School Of Medicine Jun 2021 - PresentChapel Hill, North Carolina, United States• Provided appropriate training and tools for study team members (new hires)• Maintained accuracy of DOA logs• Assisted PI in ensuring that all key personnel or persons 'engaged' in the research project have met training requirements in accordance with federal regulations and university policies and procedures.• Established partnerships with 3 external organizations to facilitate collaborative research recruitment efforts.• Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical studies• Maximized operational efficiency by developing and maintaining SOPs for various aspects of the clinical research process.• Increased patient retention rates within studies by fostering strong relationships with participants and addressing their concerns promptly.• Improved minority patient enrollment rates by effectively communicating the benefits and risks associated with participating in clinical trials.• Managed enrollment timelines for multiple concurrent studies, ensuring recruitment is aligned with project goals.• Reduced study deviations by implementing strict quality control measures and providing continuous feedback to clinical team.• Conducted trials to evaluate the efficacy of drug treatments for depression.• Acted team leader in group projects, delegating tasks and providing feedback.• Identified issues, analyzed information and provided solutions to problems.• Demonstrated respect, friendliness and willingness to help wherever needed.• Developed strong communication and organizational skills through working on group projects.• Demonstrated strong organizational and time management skills while managing multiple projects.• Exercised leadership capabilities by successfully motivating and inspiring others. -
Clinical Research CoordinatorUniversity Of North Carolina At Chapel Hill School Of Medicine Apr 2017 - Jun 2021Department Of Psychiatry, Center For Women'S Mood Disorders•Handled 5 successful clinical trials related to depression•Worked independently providing study coordination, including screening of potential patients for protocol eligibility and participating in the informed consent process.•Developed, managed and trained in-house SOPs for phase II/III EGF cancer vaccine.•Reduced data entry errors by implementing stringent quality control measures throughout study lifecycle.•Monitored patient safety throughout clinical trials and reported any adverse events.•Managed patient recruitment, informed consent process and data entry to support trial objectives.•Increased participant retention rates through proactive follow-up efforts and regular engagement activities.•Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.•Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.•Improved recruitment rates by developing and implementing effective patient outreach strategies.
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Health Education AssociateDurham County Department Of Public Health Mar 2016 - Apr 2016Durham, Nc-Conducted literature reviews on evidence-based Chronic Disease Self-Management programs.-Obtained secondary data on chronic diseases that most impact Durham County.-Conducted key informant interviews-Conducted and compiled needs assessment report.-Developed logic models-Developed evaluation instruments for target population.-Planned, developed, and implemented educational webinars.-Coordinated with lay representatives through volunteer programs, community organizations, and committees.-Formed partnerships with community organizations for recruitment and referrals into the Chronic Disease Self-Management Programs (CDSMP).-Developed and Implemented community health education activities.Compiled recruitment letters.-Completed Diabetes Self-Management training.
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Accure Research AssistantHealth Promotion Disease Prevention Office (Hpdp) May 2014 - Apr 2016Chapel Hill, Nc•Assisted IT with the efficiency of EPIC and Real-time Registry data.•Assisted nurse navigator with appointment categorization and screening of eligible Breast and Lung Cancer patients for the ACCURE study.•Created and maintained the accuracy of the code book, displaying appointments relevant to ACCURE study and useful to Cone Health hospital.•Conducted and transcribed nurse navigator Interviews•Coded nurse navigator communication notes using Atlas.ti and CBPR method.•Conducted qualitative data analysis•Assisted with taking meeting minutes on weekly steering committee conference calls•Assisted and Co-authored on APHA presentation of nurse navigation and real-time cancer registry: Informing policy with race-specific findings on equity in re-standards of cancer care•Participated in meetings surrounding radiation appointments (i.e. Herceptin)•Conducted electronic medical record reviews by screening patient’s medical charts to identify the types of appointments relevant to their treatment such as (chemotherapy, radiation, CT scan, etc). •Identified and categorized over 170 appointments matching within 31 categories of the American Cancer Society standards of care appointments.•Reviewed and coded over 741 out of 1,486 nurse medical chart notes for year 1 (April 3, 2013-June 30, 2014)•Finalized and uploaded into Atlas.ti the code book used in analyzing navigator communication notes•Produced an Academic-Community Coder Discrepancy Table (unique to CBPR projects), to clarify inter-coder reliability•Conducted a literature review on the state of nurse navigation nationally
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Nurse Tech/ Unit CoordinatorDuke University Medical Center May 2011 - Dec 2012•Perform basic clerical duties by answering phones, make copies, fax, and print out staff schedules.•Ensure client confidentiality and respect for patient privacy.•Inventory, restock and order supplies.•Assist with admission, transfer, and discharge of patients.•Provide direct patient care under the supervision of a registered nurse.•Document patient care given according to policy and procedure guidelines.•Collect and deliver specimens for lab tests (occult blood, UA, Sputum, stool, Blood platelets).•Perform and record vital signs, and perform Accu checks•Reinforce patient teaching initiated by the nursing staff.•Monitor and report health changes in the patient’s condition to appropriate personnel. •Set-up telemetry monitoring•Record input and output on all patients
Jamie Steed Skills
Jamie Steed Education Details
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Public Health Education And Promotion
Frequently Asked Questions about Jamie Steed
What company does Jamie Steed work for?
Jamie Steed works for University Of North Carolina At Chapel Hill School Of Medicine
What is Jamie Steed's role at the current company?
Jamie Steed's current role is Clinical Research Specialist.
What schools did Jamie Steed attend?
Jamie Steed attended North Carolina Central University.
What are some of Jamie Steed's interests?
Jamie Steed has interest in Children, Economic Empowerment, Civil Rights And Social Action, Environment, Education, Poverty Alleviation, Human Rights, Arts And Culture, Health.
What skills is Jamie Steed known for?
Jamie Steed has skills like Microsoft Word, Microsoft Excel, Public Speaking, Powerpoint, Research, Public Health, Data Coding, Data Analysis, Event Planning, Community Outreach, Leadership, Healthcare.
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