Robert C. Email & Phone Number

Andover, Ma

Cambridge, Ma

Greater Boston Area

Norwood, Massachusetts

Clinical Research Associate: Corbus Pharmaceuticals1. The primary point of contact for investigator sites, and is responsible for ensuring the clinical trial is being conducted according to CFR, ICH guidelines and GCP. 2. Is responsible for the efficient execution of monitoring and other clinical trial management activities, tracks the progress of assigned studies/projects. Proactively identifies potential challenges and develops appropriate actions to resolve issues and achieve target objectives.• Performs investigator site pre-study site qualification visits including collection of site regulatory documents. • Assists with site start-up activities including: site contracts and budget development/negotiation, preparation of IRB submissions (including follow through to ensure successful outcome). • Ensures investigator sites have met all contractual and regulatory requirements for site initiation and first release of study drug. • Assists in the development of study/program plans (e.g., Monitoring Plan, eCRF Completion Guidelines, Data Management Plan, Safety Management Plan, etc.). • Manages patient recruitment strategies, or pro-actively identifies barriers to recruitment and propose solutions (e.g., study site webinars, newsletters, or other potential creative solutions). • Monitors recruitment, data quality, and patient safety while on site and remotely through EDC systems and direct site communication. • Liaise with study site personnel to ensure timely and correct entry of data into eCRF, including the timely resolution of data queries. • Maintains project file.• Identifies and completes follow- up of SAEs at study sites. • Ensures appropriate and timely submission of documents to the Trial Master File.

Boston

 Collaborates with pharmecutical sponsors (e.g., Regeneron and Takeda) to manage research studies and collect data adhering to GCP, FDA, ICH, and applicable laws and regulations Conducts research on non-interventional protocols in collaboration with study physicians Collaborates on decisions and assists with appropriate amendments to the protocol via BWH and DFCI-IRB Recruits patients directly from DFCI, BWH, and the general public for a study on pain perception and hormone treatment in men with prostate cancer Screens study participants over the phone and in person to guide study physicians through eligibility determination of appropriate participants Administers consent to study subjects  Conducts study visits per protocol and ensures standardized data collection Collaborates to create and maintain study specific electronic databases  Guides work study students, interns, and junior colleagues in protocol specific goals including data collection and entry  Prepares study summary reports regarding recruitment status and study’s progress. Takes an active role in subject recruitment methods Stays current and up to date with position’s trainings and certifications Honors and maintains confidentiality for protected health information of participants and hospital patients at all times Co-authorship on the publication: “A Subset of Men With Age-Related Decline in Testosterone Have Gonadotroph Autoantibodies.”

Clinical Affective Psychophysiology Laboratory

• Researched and wrote a scientific journal paper investigating associations related to anhedonia, depression, life stress, and social rejection• Presented clinical scientific research during conferences at Stanford, University of California, Berkeley, University of California, Los Angeles and the Western Psychological Association Conference, in San Francisco. • Created, edited graphs and prepared materials to be presented using PowerPoint, SPSS, and other research and analytical tools

Los Angeles

• Prepared syllabus and maintained student websites• Edited professors upcoming book; Voices of Pain, Voices of Hope: Students Speak About Racism, fourth edition• Researched preparation for journal entries, as well as citations and referencing• Additional non-professorship work included private and personal business, such as work on diversity training and private practice Clinical Marriage and Family Therapy websites

Los Angeles

• Involved in a study examining individual physiological differences between clinical patients with schizophrenia in varying phases along with ethnicity gender and socioeconomic matched control groups while going through stressful experimental conditions• Connecting patients to physiological measures such as EEG, heart monitors, and galvanic skin response. • Obtaining and logging cortisol samples from participants and maintaining privacy by using participant numbers • Asking medically and scientifically relevant questions and administering psychological metric forms such as the Beck Depression Inventory (BDI) and the State Trait Anxiety inventory (STAI)• Data entry and processing using excel• Running and setting up and performing experiments using the Social Trier Stress paradigm as well as providing directions for the Oral Mental Arithmetic tasks• Running computer programs for participants to set up tasks involving memory

Agoura Hills

Assistant Store Manager• Involved with training, evaluating, scheduling, and ensuring product and customer experience quality in the busiest store in the district• Managed the store’s financial performance • Operated and taught others to operate and maintain cash registers, espresso machines, and other professional, industrial equipment• Assisted new employees by training them on both technical and customer-service skills

Master Of Business Administration - Mba, Focus Area Finance

Honors B.A., Psychology

Activities and Societies: Honors program, independent research, and multiple research associations. uclastresslab.org