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Jessica Claire
  • , , 100 Montgomery St. 10th Floor
  • H: (555) 432-1000
  • C:
  • resumesample@example.com
  • Date of Birth:
  • India:
  • :
  • single:
Professional Summary

Focused 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 20+ years of related experience to a challenging new role. Skilled at collecting specimens, dispensing medications and consulting with patients during the course of clinical research trials. Experienced in coordinating schedules, results and documentation. Knowledgeable Certified Clinical Research Coordinator adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues. Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Certified in Clinical Research Trials. Dedicated Research professional with history of meeting company goals utilizing consistent and organized practices. Skilled in working under pressure and adapting to new situations and challenges to best enhance the organizational brand. Reliable employee seeking Clinical Research position. Offering excellent communication and good judgment. Enthusiastic Certified Research Coordinator eager to contribute to team success through hard work, attention to detail and excellent organizational skills. Clear understanding of protocol required and training in specific protocol procedures. Motivated to learn, grow and excel in research. Hardworking and passionate job seeker with strong organizational skills eager to secure Clinical Research position. Ready to help team achieve company goals. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.

Skills
  • Trial management
  • Informed consent
  • Research SOPs understanding
  • Study protocols
  • Specimen collections
  • Medication dispensing
  • Schedule Coordination
  • Good Clinical Practices
  • Written Communication
  • Decision Making
  • Good Telephone Etiquette
  • Flexible and Adaptable
  • Critical Thinking
  • Teamwork and Collaboration
  • Organization and Time Management
  • Active Listening
  • Maintenance and Repair
  • MS Office
Work History
Certified Clinical Research Coordinator, 06/2019 - 09/2021
Mayo Clinic Morgan, MN,
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • 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.
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • Gathered, processed and shipped lab specimens.
  • Collected, evaluated and modeled collected data.
  • Quickly learned new skills and applied them to daily tasks, improving efficiency and productivity.
  • Carried out day-day-day duties accurately and efficiently.
  • Demonstrated respect, friendliness and willingness to help wherever needed.
  • Worked flexible hours; night, weekend, and holiday shifts.
  • Performed duties in accordance with applicable standards, policies and regulatory guidelines to promote safe working environment.
  • Maintained energy and enthusiasm in fast-paced environment.
  • Proved successful working within tight deadlines and fast-paced atmosphere.
  • Used critical thinking to break down problems, evaluate solutions and make decisions.
  • Offered friendly and efficient service to customers, handled challenging situations with ease.
  • Developed and maintained courteous and effective working relationships.
  • Coordinated clinical trials focused on disorders such as Chronic Kidney Disease and Anemia in Chronic Kidney Disease.
Certified Clinical Research Coordinator, 08/2018 - 05/2019
Mayo Clinic New Auburn, WI,
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • 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.
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • Gathered, processed and shipped lab specimens.
  • Collected, evaluated and modeled collected data.
  • Coordinated clinical trials focused on disorders such as Adult and Pediatric Asthma and Adult Diabetes Mellitus.
  • Quickly learned new skills and applied them to daily tasks, improving efficiency and productivity.
  • Carried out day-day-day duties accurately and efficiently.
  • Demonstrated respect, friendliness and willingness to help wherever needed.
  • Worked flexible hours; night, weekend, and holiday shifts.
  • Performed duties in accordance with applicable standards, policies and regulatory guidelines to promote safe working environment.
  • Maintained energy and enthusiasm in fast-paced environment.
  • Proved successful working within tight deadlines and fast-paced atmosphere.
  • Used critical thinking to break down problems, evaluate solutions and make decisions.
  • Offered friendly and efficient service to customers, handled challenging situations with ease.
  • Developed and maintained courteous and effective working relationships.
Certified Clinical Research Coordinator, 10/2015 - 10/2017
Mayo Clinic New Market, MN,
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • 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.
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • Gathered, processed and shipped lab specimens.
  • Collected, evaluated and modeled collected data.
  • Coordinated clinical trials focused on disorders such as Adult and Pediatric ADHD and Narcolepsy.
  • Quickly learned new skills and applied them to daily tasks, improving efficiency and productivity.
  • Carried out day-day-day duties accurately and efficiently.
  • Demonstrated respect, friendliness and willingness to help wherever needed.
  • Worked flexible hours; night, weekend, and holiday shifts.
  • Performed duties in accordance with applicable standards, policies and regulatory guidelines to promote safe working environment.
  • Maintained energy and enthusiasm in fast-paced environment.
  • Proved successful working within tight deadlines and fast-paced atmosphere.
  • Used critical thinking to break down problems, evaluate solutions and make decisions.
  • Offered friendly and efficient service to customers, handled challenging situations with ease.
  • Developed and maintained courteous and effective working relationships.
Clinical Research Coordinator, 08/2012 - 10/2015
Columbia University New York, NY,
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Collected data and followed research protocols, operations manuals and case report form requirements.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
  • Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
  • Followed informed consent processes and maintained records.
  • Gathered, processed and shipped lab specimens.
  • Collected, evaluated and modeled collected data.
  • Coordinated clinical trials focused on disorders such as Multiple Cancer Diagnosis and Anemia Associated with Cancer Therapies.
  • Monitored unit budget to meet financial objectives for spend rate and funding.
  • Quickly learned new skills and applied them to daily tasks, improving efficiency and productivity.
  • Carried out day-day-day duties accurately and efficiently.
  • Demonstrated respect, friendliness and willingness to help wherever needed.
  • Worked flexible hours; night, weekend, and holiday shifts.
  • Performed duties in accordance with applicable standards, policies and regulatory guidelines to promote safe working environment.
  • Maintained energy and enthusiasm in fast-paced environment.
  • Proved successful working within tight deadlines and fast-paced atmosphere.
  • Used critical thinking to break down problems, evaluate solutions and make decisions.
  • Offered friendly and efficient service to customers, handled challenging situations with ease.
  • Developed and maintained courteous and effective working relationships.
Education
Certified Medical Assistant: Health Care, Expected in
-
Texas Careers Institue - San Antonio, TX,
GPA:
Studies in Real Estate: Real Estate, Expected in
-
Elizabethtown Community And Technical College - Elizabethtown, KY
GPA:
Certifications
  • Certified Clinical Research Coordinator - 2015
Additional Information

Integrity + Work Ethic + Positive Attitude = Success

“The greatest rewards come when you give of yourself. It's about bettering the lives of others, being part of something bigger than yourself, and making a positive difference.” -Nick Vujicic

I am a detail-oriented clinical researcher who has fine-tuned my skills to be proficient in my career working on phase 1-4 clinical studies. I excel at critical thinking to solve complex problems, team work, leadership, accountability and interpersonal communication. I'm passionate, organized and the hardest worker you'll ever meet. All of these skills propel me towards success within the pharmaceutical industry.

I work or have worked on the following indications: Diabetes, Hypoglycemia, Anemia, DVT Prophylaxis post op, Osteoarthritis, Gout, Rheumatoid Arthritis, Adult and Pediatric Neurological disorders, Chronic Kidney Disease/Dialysis, Adult and Pediatric Respiratory Disorders, and Cancer.

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Resume Overview

School Attended

  • Texas Careers Institue
  • Elizabethtown Community And Technical College

Job Titles Held:

  • Certified Clinical Research Coordinator
  • Certified Clinical Research Coordinator
  • Certified Clinical Research Coordinator
  • Clinical Research Coordinator

Degrees

  • Certified Medical Assistant
  • Studies in Real Estate

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