Suzanne Moritz Email & Phone Number

Rahway, New Jersey, Us

Rahway, New Jersey, Us

Work as a Senior CRA on various oncology clinical trials. Conduct site validation, initiation, interim monitoring and close-out visits of Phase I through Phase III clinical trials in accordance with GCPs. Assist with study start-up and closure activities, conduct all site management activities for assigned sites, conduct trial master file audits and perform file maintenance, act as regulatory affairs liaison, and attend Investigator’s Meetings.

Raleigh, North Carolina, Us

Worked on clinical trials of various vaccines including the therapeutic areas of: COVID-19, Yellow Fever and various childhood vaccines. Conducted site selection, initiation, interim monitoring and close-out visits of Phase I through Phase III clinical trials in accordance with GCPs. Assisted with study start-up and closure activities, conducted all site management activities for assigned sites, conducted trial master file audits and performed file maintenance, acted as regulatory affairs liaison, and attended Investigator’s Meetings. Acted as mentor to newly hired CRAs and less experienced CRAs.

Morrisville, Nc, Us

Conducted site selection, initiation, interim monitoring and close-out visits of Phase II and Phase III clinical trials in accordance with GCPs in therapeutic areas and Rare Diseases including Duchenne Muscular Dystrophy, postpartum depression, Myasthenia Gravis, and Neuromyelitis Optica. Assisted with study start-up and closure activities, conducted all site management activities for assigned sites, conducted trial master file audits and performed file maintenance, acted as regulatory affairs liaison, and was present at Investigator’s Meetings. Acted as mentor to newly hired CRAs and less experienced CRAs

Durham, North Carolina, Us

Conducted site selection, initiation, interim monitoring and close-out visits of Phase III, IV and real-world evidence and outcomes research trials in accordance with GCPs in therapeutic areas including: depression (MDD), Leber's Hereditary Optic Neuropathy (LHON), dermatology, arthritis, and oncology. Acted as mentor to newly hired and less experienced CRAs.

Durham, North Carolina, Us

Ensured clinical research studies are conducted in accordance with the protocol, SOPs, good clinical practices and regulatory requirements while working with participating sites in various therapeutic areas. Performed site selection, initiation, interim monitoring, and close-out visits.

Ashburn, Va, Us

Provided individual and group instructional support to Autistic students in 3rd-5th grade self-contained classroom and also within the general education setting. Implement and apply behavior management techniques and plans. Collected and recorded student data.

Northbrook, Il, Us

Handled high volume of inbound and outbound calls in fast-paced environment. Demonstrated best-in-class customer service to enhance client satisfaction, retention and referrals. Contributed to development of direct and digital marketing campaigns.

Seongnam-Si, Gyeonggi-Do, Kr

Monitored Phase I-!V clinical research drug trials in therapeutic areas including: oncology, Hepatitis C, MPS VI. Performed pre-study, initiation, interim monitoring and close-out visits, Assisted in protocol development, CRFs/guidelines, and study-specific forms. Performed investigator recruitment, conducted regulatory file audits and presented at Investigators' Meetings.

Established a West Coast client base of pharmaceutical and biotechnology companies to market and sell the clinical research services of this CRO. Promoted the CRO and educated clients regarding pre-clinical, analytical, and clinical service offerings.Managed the proposal team process including obtaining input from clinical, data management, regulatory personnel to integrate and deliver proposals.

Princeton, New Jersey, Us

Worked on new business development from biotechnology and pharmaceutical companies for the West Coast operations of this CRO. Managed proposal team process including obtaining input from clinical operations, data management, bio-statistical, programming, regulatory, and business development personnel to integrate and deliver the proposals.

Seongnam-Si, Gyeonggi-Do, Kr

Responsible for establishing a West Coast client base of pharmaceutical and biotechnology companies to market and sell the clinical research services provided by this start-up CRO. Also performed various monitoring functions including reviewing CRFs for an HIV protease inhibitor study, monitoring a dermatology study and performing pre-study visits for an HIV comparative study.

Wilmington, Nc, Us

Monitored Phase III and Phase IV clinical research drug trials in therapeutic areas including: oncology, pain management, and arthritis.

Worked as Administrative Resident while completing my MHA. Coordinated health system's United Way campaign, served as a member of steering committee and project team charged with implementing Patient Focused care hospital-wide, served as member of steering committees for developing a charitable giving Foundation and with the formation of a Physician Hospital Organization. Led the Emergency Room registration process, including managing 24 employees.

Master Of Health Administration (Mha)

Bachelor Of Science (Bs), Psychology, Minor In Special Education