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Senior Clinical Research Coordinator Resume Example

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JC
Jessica Claire
, , 100 Montgomery St. 10th Floor (555) 432-1000, resumesample@example.com
Professional Summary

Focused and Detail-oriented Clinical Research Coordinator well-versed in study protocols, standard operating procedures and general trial oversight. Excellent problem-solving abilities with a detail-oriented nature. Ready to bring 12 years of related experience to a challenging new role. Highly organized and thorough with good planning and problem-solving abilities. Communicate effectively with study participants, colleagues, vendors, and study monitors.

Skills
  • Research SOPs understanding
  • Medication dispensing
  • Informed consent
  • Good Clinical Practices
  • Data Collection
  • Specimen collection
  • Microsoft Office
  • Organization skills
  • Time Management
  • Strong Work Ethic
Work History
06/2021 to Current Senior Clinical Research Coordinator Drug Information Association Inc | Cedar Rapids, IA,
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Gathered, processed and shipped lab specimens.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Coordinated clinical trials focused on disorders such as Liver Disease and Gastroenterology.
  • Collected data and followed research protocols, operations manuals and case report form requirements.
  • Followed informed consent processes and maintained records.
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • Maintained working knowledge of Regulatory guidelines, compliance with applicable ICH-GCP guidelines, and local regulatory requirements, SOP, and study specific procedures.
04/2019 to 07/2020 Research Coordinator III (Pediatric Dept.) Baylor College Of Medicine | City, STATE,
  • Coordinated all administrative functions for planned studies, including protocol development, equipment preparation and materials purchasing.
  • Execute clinical trials on site and remotely
  • Ensure compliance with NIH and IRB regulation
  • Assess hospital record or each patient, review databases and referral leads to screen for potential eligible patients
  • Adhered to standards in all areas, including data collection, research protocols, and regulatory reporting
  • Refined and contributed to special data entry projects of current & previous study trials.
  • Maintenance of study regulatory document, including screening, enrollment logs & study identification logs
  • Assist PI in submission in most reports, including adverse events, non-compliance, or any other unanticipated issues
  • Implemented new data base from scratch
  • Worked closely with PI and other hospital staff to maintain optimum levels of communication to effectively and efficiently complete projects
  • Used critical thinking to break down problems, evaluate solutions and make decisions
02/2008 to 10/2018 Research Coordinator III (Psychiatric Dept.) Baylor College Of Medicine | City, STATE,
  • Coordinated clinical trials focused on Stimulant Addiction, which included, overseeing clinical assessment of patients participating in clinical trial studies of Cocaine, Methadone, and Nicotine.
  • Adhered to standards in all areas, including data collection, research protocols and regulatory reporting.
  • Expertly conducted full range of patient and protocol assessments, including safety and efficacy, vital signs, administering study medications, and EKGs.
  • Assisted in implementing and developing patient recruitment plans to ensure clinical trial success while training students on patient care, electronic forms & management processes to ensure success of trials
  • Maintained working knowledge of Regulatory guidelines, compliance with applicable ICH-GCP guidelines, and local regulatory requirements, SOP, and study specific procedures.
  • Conducted in house and sponsored clinical trial audits
  • Collaborated with physicians, hospital support staff and drug companies to ensure efficient implementation of clinical trial protocols
  • Collected, process and ship biological specimens according to study protocol
  • Evaluated and analyzed clinical research data
  • Quality Control for the entire lab for 4 years
  • Perform billing reconciliation when applicable
  • Actively listened to patients, handled concerns quickly and escalated major issues to supervisor or PI
Education
Expected in 04/2022 Associate of Applied Science | Education Lone Star College System, Spring, TX GPA:

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Resume Overview

School Attended
  • Lone Star College System
Job Titles Held:
  • Senior Clinical Research Coordinator
  • Research Coordinator III (Pediatric Dept.)
  • Research Coordinator III (Psychiatric Dept.)
Degrees
  • Associate of Applied Science

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