- , , 100 Montgomery St. 10th Floor
- (555) 432-1000
- resumesample@example.com
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.
|
|
Arkansas Urology – Bentonville, AR,
- 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.
Arkansas Urology – Benton, AR,
- 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.
Arkansas Urology – Pine Bluff, AR,
- 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.
Retina Vitreous Associates – 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.
Metro Baptis - Madison, TN,
- Certified Phlebotomy
- Training:
- Human Research
- Good Clinical Practice
- Protecting Human Research Participants
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.
By clicking Customize This Resume, you agree to our Terms of Use and Privacy Policy
Disclaimer
Resumes, and other information uploaded or provided by the user, are considered User Content governed by our Terms & Conditions. As such, it is not owned by us, and it is the user who retains ownership over such content.
How this resume score
could be improved?
Many factors go into creating a strong resume. Here are a few tweaks that could improve the score of this resume:
resume Strength
- Formatting
- Length
- Personalization
- Strong Summary
- Target Job
Resume Overview
School Attended
- Metro Baptis
Job Titles Held:
- Clinical Research Coordinator/Director
- Clinical Research Coordinator
- Clinical Research Coordinator
- Clinical Research Coordinator
Degrees
- High School Diploma
By clicking Customize This Resume, you agree to our Terms of Use and Privacy Policy
Similar Resume
medical affairs research operations intern executive director, sr. director, senior medical monitor, project manager remote study specialist, clinical team manager, study coordinator, project assistant, executive assistant, strategic feasibility specialist
PPD, Inc CRA
Wilmington, North Carolina
laboratory manager and translational research and clinical coordinator - director veena singh, labpmm
NA
Carlsbad, California
clinical research coordinator/director of clinical operations
St. Dominic Health Systems
Jackson, Mississippi
