Jessica Claire
Montgomery Street, San Francisco, CA 94105 (555) 432-1000, resumesample@example.com
Summary
Dedicated Clinical Research Coordinator with over 20 years of experience in complying with study protocols, standard operating procedures and good clinical practices. Practiced problem-solver with strong attention to detail. Knowledge of FDA and GCP principles and regulations. Committed to providing support to the project team and executing responsibilities as instructed.
Skills
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Experience
10/2018 to Current Research Coordinator Balyasny Asset Management | New York, NY,
- Recognized issues and developed immediate resolutions to address and alleviate concerns.
- Adhered to standards in areas involving data collection, research protocols and regulatory reporting.
- Obtained informed consent of research subjects or guardians
- Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
- Conducted informed consent presentations and maintained documentation.
- 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.
- Organized, analyzed and modeled study data.
- Collected, processed and delivered specimens from trial participants.
- Detailed results and conclusions in professionally-prepared documents, reports and presentations.
- Checked electronic data capturing systems for integrity and compliance.
- Maintained laboratory record system to document key information on specimen collection, identification, quality control and other factors.
- Sanitized workstations and salon equipment to reduce risk of infection.
- Reviewed packages and medication bottles for proper labeling before distributing to patients.
- Checked medications for content, accuracy and completeness of drug packaging and labeling.
- Maintained compliance with state and federal drug laws.
04/2011 to 09/2018 Research Coordinator/ Office Manager Balyasny Asset Management | Austin, TX,
- Research Allergy, Asthma and Sinus Assoc.
- Oversaw receiving and organizing correspondence, answering and forwarding calls and creating business letters and records.
- Keyed in customer contacts and delivery dates to update details in company databases.
- Managed office inventory and placed new supply orders.
- Handled scheduling and managed timely and effective allocation of resources and calendars.
- Trained and mentored administrative staff members in company policies, daily task execution and industry best practices.
- Coordinated office activities and operations to secure efficiency and compliance with company policies.
- Reduced financial discrepancies by accurately managing accounting documentation.
- Mentored and provided ongoing support to research team, providing training in research design and conduct.
- Kept patient care protocols and clinical trial operations in compliance.
- Adhered to standards in areas involving data collection, research protocols and regulatory reporting.
- Obtained informed consent of research subjects or guardians
- Performed preliminary physical tests to accurately record results in patient history summary.
- Educated patients about medications, procedures and physician's instructions.
- Maintained inventory, vaccination and product expiration logs to record updated documentation for tracking purposes.
- Efficiently performed insurance verification and pre-certification and pre-authorization functions.
02/2007 to 04/2011 Research Coordinator Balyasny Asset Management | Boston, MA,
- Juggled multiple projects and tasks to ensure high quality and timely delivery.
- Prioritized and organized tasks to efficiently accomplish service goals.
- Worked closely with team members to deliver project requirements, develop solutions and meet deadlines.
- Worked successfully with diverse group of coworkers to accomplish goals and address issues related to our products and services.
- Managed clinical research trials involving women's health, neurological and gynecological disorders.
12/2004 to 02/2007 Research Coordinator Mid Atlantic Retina | Mays Landing, NJ,
- Cleaned and sterilized lab area, tools and equipment.
- Followed strict aseptic techniques to protect patients when collecting blood and tissue samples.
- Drew blood from patients to collect samples using venipuncture and following aseptic techniques.
- Documented and updated patient data on electronic medical charts, maintaining accuracy and confidentiality.
- Observed and recorded vital signs and reported changes to physicians or nurses.
- Adhered to all safety and infection control precautions and regulations.
- Supported healthcare teams in consistently delivering timely and quality care according to company standards.
- Obtained informed consent of research subjects or guardians
- 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.
07/2001 to 12/2004 Research Assistant Medical Research Unlimited | City, STATE,
- Reviewed new research literature to remain current with examination procedures.
- Conducted qualitative and quantitative analysis on data assigned.
- Used Microsoft Word and PowerPoint to prepare reports, presentations and research results.
- Completed research assignments by organizing data, generating spreadsheets and drafting reports.
- Generated reports and made recommendations based on research outcomes.
- Prepared documentation of research procedures and data gathered for dissemination to staff members.
- Researched data processing operations and conducted proof of concept monitoring after new process implementation.
- Monitored experiments and maintained detailed records of experiments and outcomes.
- Organized and maintained records, inventory and materials.
- Assisted in research for development of new products and processes.
- Adhered to standards in areas involving data collection, research protocols and regulatory reporting.
- Managed informed consent forms, personal waivers and other critical paperwork.
- Designed survey instruments and questionnaires to obtain desired research data.
Education and Training
Expected in 12/2020 Associate Degree in Healthcare Administration | Healthcare Colorado Christian University, Denver, CO
Expected in 06/2008 Certified Clinical Research Coordinator | ACRP, ,
Bachelor of Science | Clinical Research Administrator George Washington University, The, Washington, DC
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Resume Overview
School Attended
- Colorado Christian University
- ACRP
- George Washington University, The
Job Titles Held:
- Research Coordinator
- Research Coordinator/ Office Manager
- Research Coordinator
- Research Coordinator
- Research Assistant
Degrees
- Associate Degree in Healthcare Administration
- Certified Clinical Research Coordinator
- Bachelor of Science
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