Clinical Research Study Assistant involved in Alzheimer's disease research collecting samples and data. Participating in study protocols and maintaining participant interactions.
Responsibilities
Participates in recruitment of study participants as identified in related protocol
Visits with study participants to explain study, screens for eligibility and obtains informed consent of participants
Processes blood samples, including centrifugation of blood samples and aliquoting plasma into tubes
Completes all necessary paperwork/documentation according to study protocol
Interviews study subjects and schedules follow-ups as needed
Performs basic/scripted assessments to confirm eligibility to participate in study
Collects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources
Prepares appropriate reports and documentation as necessary
Performs other duties as assigned
Requirements
High school diploma or equivalent high school certification or combination of education and/or experience
Basic Life Support certification must be obtained within one month of hire date
2 years of administrative or research experience
Not applicable skills listed
A driver's license is not required for this position
Benefits
Up to 22 days of vacation
10 recognized holidays
Sick time
Competitive health insurance packages with priority appointments and lower copays/coinsurance
Free Metro transit U-Pass for eligible employees
Defined contribution (403(b)) Retirement Savings Plan with university contributions starting at 7%
Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians
4 weeks of caregiver leave to bond with your new child
Covers the cost of tuition for you and your family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years
Associate HR Partner supporting employee operations at CPS Clinical Research Units. Providing HR guidance and managing employee relations in a clinical environment with on - site presence.
Oncology Clinical Research Coordinator at WVU managing clinical trials and ensuring protocol compliance. Collaborating with research staff and healthcare providers while advocating for ethical participant care.
Clinical Research Coordinator supporting clinical research for pediatric care at Shriners Children’s. Ensuring compliance with research protocols and collaborating with clinical teams in Pasadena.
Clinical Research Coordinator managing aspects of clinical trials at Winship Cancer Institute. Handling data management, participant interface, and overseeing trial compliance in Atlanta.
Feasibility Manager at Novo Nordisk optimizing clinical trials through data analysis and strategic partnerships across South Africa. Driving site selection and operational readiness for impactful clinical development.
Clinical Research Coordinator managing overall coordination and implementation of clinical trials. Collaborating with investigators to ensure compliance with study protocols and maintaining accurate subject records.
Clinical Research Coordinator independently managing key aspects of clinical trials. Overseeing data management and ensuring compliance with study protocols and regulations.
Clinical Research Coordinator supporting pediatric research initiatives at Shriners Children's in Pasadena. Ensuring compliance with protocols and managing research data collection.
Associate Clinical Research Director providing medical expertise to clinical studies and supporting development activities in a global biopharmaceutical company. Collaborating with stakeholders to ensure optimal study execution.
Clinical Research Coordinator, Sr advancing federally funded and industry - sponsored neonatal and perinatal research at Duke. Overseeing regulatory compliance and mentoring research staff in a medical center.