Nicole Ferguson Email & Phone Number

Nashville, Tn, Us

• Collaborated with other advisors to support the Women in Leadership Executive program at the University of Tennessee, Knoxville.• Provided valuable insights and mentorship based on real-world experiences to empower women in leadership roles.• Contributed to the program's success by sharing industry knowledge and fostering a supportive environment for professional growth.

Nashville, Tennessee, United States

Strategic Solution Division (SSD) Janssen

Nashville, Tennessee, United States

Strategic Solution Division (SSD) Janssen

Nashville, Tennessee

Nashville, Tennessee

Greater Nashville Area, Tn

- Conduct the clinical monitoring aspect of designated projects- Perform qualification visits including site facilities inspection, SRP document collection, and establish a site recruitment plan in collaboration with the site- Perform initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines using a thorough understanding of therapeutic indications and study hypothesis- Perform clinical on-site monitoring activities in accordance with applicable SOPs (drive patient recruitment, source data verification, drug accountability, data collection)- Monitor patient safety on-site (review for missing SAEs, AEs, ConMeds) and address protocol violations- Conduct study-specific training of site staff and build cooperative and constructive relationships with investigators and site staff- Collect regulatory documentation- Review and verify the completeness and quality of on-site files- Update all relevant tracking system on an ongoing basis- Conduct drug accountability - Collaborate with Clinical Monitoring Associate regarding site issues (non-responsiveness, protocol deviations concerns, quality issues)- Participate in company - required training programs

Nashville, Tn

A clinical research associate (CRA) is a professional who monitors the administration and progress of a clinical trial (pharmaceuticals, biologics, or devices) on behalf of a sponsor. A CRA can monitor between 2-4 studies depending upon the indication and timeframe of the study.

Greater Nashville Area, Tn

A clinical research assistant coordinators/maintains the trial master study files, initials contact with potential investigators to participate in the study, assist with audit management and response, assist in filed monitoring and liaised with other internal departments.

Greater Nashville Area, Tn

A site activation service representative collects, review, process and track regulatory/investigator documents required for study site activation, review investigative site specific patient informed consents, negotiate contracts and budgets with investigative sites and mange site address and contact information.

Greater Nashville Area, Tn

Responsible for handling customer dilemmas, educating customers on bank products and services and operate Mainframe database system regarding confidential customer profiles.

Chattanooga, Tennessee Area

Responsible for generating and auditing daily reports to help prevent fraudulent customer transactions, assist in identifying delinquent customers and train new tellers on bank polices and procedures.

Master'S Degree, Business Leadership/Strategic Leadership

Bachelor Of Applied Science (Basc), Business Administration And Management, General

Activities and Societies: Alpha Kappa Psi Business Fraternity

Post Certificate, Clinical Research Studies

High School Diploma