What are the responsibilities and job description for the Clinical Research Coordinator - Contract position at Atlas Clinical Research?
This is a 5 month contract position in Buffalo, NY. Must be able to work M-R 7:30 am to 4:45 pm and F 7:30 am to 12:30 pm.
Job Summary
The Study Coordinator works closely with the Principal Investigator managing study conduct from study selection through study closeout. The Study Coordinator is responsible for the quality and integrity of their assigned clinical studies in accordance with Good Clinical Practice (GCP) and applicable regulations.
Key Responsibilities
- Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including participating in the informed consent process, coordinating, and performing all study visit procedures per protocol, managing Investigational Product and study related supplies and equipment, assisting with monitoring visits, attending Investigator Meetings, and assisting with query resolution, as required.
- Provide the highest level of care and excellent customer service for study participants.
- Collaborate with lab staff to plan for and manage laboratory samples throughout the length of the study, including review of the laboratory manual.
- Ensure study drug is dispensed, accounted for and returned to the Sponsor per protocol.
- Ensure Serious Adverse Events (SAE’s) are reported to Principal Investigator, Sponsor, and IRB (through Regulatory) within 24 hours of site being notified of event, including collecting all required information for initial and followup reporting.
- Ensure visit logs and CTMS visit status are accurate and complete.
- Facilitate ongoing Quality Assurance (QA) review of studies, in collaboration with the QA department, including assisting with risk assessments, root cause analysis, and development of corrective and preventative actions as applicable.
Qualifications
- Excellent verbal and written communication skills.
- Excellent interpersonal and customer service skills.
- Excellent organizational skills and attention to detail.
- Excellent time management skills with a proven ability to meet deadlines.
- Strong analytical and problemsolving skills.
- Ability to prioritize tasks and to delegate them when appropriate.
- Ability to function well in a highpaced environment
Education and Experience
- 4year degree in related field or NYS LPN License required, or related experience as a clinical trial coordinator.
- At least three years’ experience in clinical research setting.
- CCRC preferred.
About Atlas Clinical Research
Atlas Clinical Research is a leading Private Equity (PE)-backed clinical research site network, dedicated to transforming the healthcare landscape through innovative research solutions. We envision a world where patients and their families have ready access to groundbreaking new treatments being developed by our sponsors, and made possible through the access, care, and support provided by our therapeutically focused clinical network. Atlas only hires candidates that reside in the following states: NY, PA, NC, GA, MA, AZ, FL and DE.