Renee Hanewich

Clinical Research Administrator

DSI Renal Institute

Providence, RI

01.2005 - 11.2007

Created detailed reports summarizing data collected from patient records, surveys, interviews.
Participated in the design of recruitment strategies for participants in clinical studies.
Analyzed data collected during a trial period using appropriate statistical methods to produce meaningful results that can be used by researchers or sponsors when making decisions about further development plans or marketing strategies associated with a drug, device, treatment under investigation.
Assisted in the development of protocol amendments as needed throughout the course of a study.
Maintained accurate records of all study-related activities including finances and communication logs.
Conducted literature reviews to identify potential sources of funding for clinical research projects.
Prepared presentations outlining project objectives, progress updates, results analysis. for internal stakeholders or external sponsors and investigators.
Monitored patient reactions to drugs and carefully documented progress of individuals participating in clinical trials.
Ensured timely completion of all deliverables associated with each project within budget constraints.
Monitored the progress of clinical studies according to established timelines and budgets.
Developed and implemented clinical research protocols, consent forms, case report forms, and other study documents.
Developed systems for tracking adverse events reported during a trial period.
Coordinated with research staff to ensure compliance with applicable laws and regulations governing clinical trials.
Managed day-to-day operations associated with ongoing clinical research projects.
Identified potential vendors providing services such as laboratory testing or imaging services required by a study protocol.
Collaborated with physicians, nurses and other healthcare professionals involved in a study to ensure high quality data collection processes are maintained throughout the duration of a trial period.
Conducted screening interviews to determine eligibility of possible subjects.
Educated participants on studies and anticipated outcomes.
Monitored subject enrollment and tracked dropout details.
Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants.
Kept patient care protocols and clinical trial operations in compliance.
Took vital signs and collected medical histories as part of study protocols.
Placed orders for medications to be used in studies.
Collected, processed and delivered specimens from trial participants.