Clinical Research Coordinator/Director Resume Example Company Name

CLINICAL RESEARCH COORDINATOR/DIRECTOR

Professional Summary

Seasoned 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 23 years of related experience to a challenging new role. 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. 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 and adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues. Enthusiastic and eager to contribute to team success through hard work, attention to detail and excellent organizational skills. Motivated to learn, grow and excel. Excellent reputation for resolving problems and improving patient satisfaction. Recognized consistently for performance excellence and contributions to success. Strengths are organization, multi tasking, communication with the doctors and companies and deadline driven.

Skills

Study protocols
Specimen collections
Good Clinical Practices
Medication dispensing
Trial management
Informed consent
Research SOPs understanding

Schedule Coordination
Multitasking abilities
Good listening skills
Excellent work ethic
Teambuilding
Self-motivated professional
Adaptability

Work History

Clinical Research Coordinator/Director, 09/2008 to Current
Company Name – City, State

Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
Collected data and followed research protocols, operations manuals and case report form requirements.
Gathered, processed and shipped lab specimens.
Followed informed consent processes and maintained records.
Maintained compliance with protocols covering patient care and clinical trial operations.
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Monitored unit budget to meet financial objectives for spend rate and funding.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Collected, evaluated and modeled collected data.
Conducted research, gathered information from multiple sources and presented results.
Completed all paperwork, recognizing any discrepancies and addressing them in a timely fashion.
Resolved problems, improved operations and provided exceptional service.
Developed and implemented performance improvement strategies and plans to promote continuous improvement.

Clinical Research Coordinator, 08/2005 to 08/2008
Company Name – City, State

Collected data and followed research protocols, operations manuals and case report form requirements.
Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
Collected, evaluated and modeled collected data.
Maintained compliance with protocols covering patient care and clinical trial operations.
Gathered, processed and shipped lab specimens.
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Monitored unit budget to meet financial objectives for spend rate and funding.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Followed informed consent processes and maintained records.
Developed team communications and information for meetings.
Resolved conflicts and negotiated mutually beneficial agreements between parties.
Used coordination and planning skills to achieve results according to schedule.
Developed and implemented performance improvement strategies and plans to promote continuous improvement.
Performed duties in accordance with all applicable standards, policies and regulatory guidelines to promote safe working environment.

Clinical Research Coordinator, 08/2004 to 05/2005
Company Name – City, State

Collected data and followed research protocols, operations manuals and case report form requirements.
Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
Collected, evaluated and modeled collected data.
Maintained compliance with protocols covering patient care and clinical trial operations.
Gathered, processed and shipped lab specimens.
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Monitored unit budget to meet financial objectives for spend rate and funding.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Followed informed consent processes and maintained records.
Developed team communications and information for meetings.
Used coordination and planning skills to achieve results according to schedule.
Actively listened to customers' requests, confirming full understanding before addressing concerns.
Performed duties in accordance with all applicable standards, policies and regulatory guidelines to promote safe working environment.

Clinical Research Coordinator, 03/2002 to 05/2005
Company Name – City, State

Collected data and followed research protocols, operations manuals and case report form requirements.
Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
Collected, evaluated and modeled collected data.
Maintained compliance with protocols covering patient care and clinical trial operations.
Gathered, processed and shipped lab specimens.
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
Monitored unit budget to meet financial objectives for spend rate and funding.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Followed informed consent processes and maintained records.
Developed team communications and information for meetings.
Used coordination and planning skills to achieve results according to schedule.
Performed duties in accordance with all applicable standards, policies and regulatory guidelines to promote safe working environment.

Education

High School Diploma: 05/1990
Metro Baptis - City

Certifications

Certified Phlebotomy
Training:
Human Research
Good Clinical Practice
Protecting Human Research Participants

Additional Information

I work with a company Targeted Medical Education and do the IRB submission for all the PI's across the US.

I also have a contract with a Breast Surgeon in CA and do his research home based.

Resume Overview

School Attended

Metro Baptis

Job Titles Held:

Clinical Research Coordinator/Director
Clinical Research Coordinator

Degrees

High School Diploma : 05/1990

Clinical Research Coordinator/Director Resume Example

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