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Xxxxxx, XXXXXX xxxxxx ￨ (xxx-xxx-xxxx ￨ abc@xyz.com

Clinical Research ￨ Oncology Clinical Trials ￨ Program Design / Administration

Clinical Site / Study Visit Coordination ￨ Internal Auditing ￨ Regulatory Compliance

Team Building ￨ Training / Development ￨ Strategic Analysis / Planning ￨ Trends Tracking

Participant Recruitment / Interviewing ￨ Community Outreach ￨ Public Health Education Advocacy

Policy / Procedure Development ￨ Multi-Process Optimization ￨ Physician Relations ￨ Staff / Patient Safety

Grant Writing ￨ Protocols Development ￨ Data Management ￨ HIPAA ￨ GCP ￨ ICH ￨ WIs ￨ FDA / Local Regulations

Highly Accomplished Clinical Research Coordinator who makes sound decisions to continually reflect positively on multi-site study initiatives in alignment with an employer s vision. Top Performer who offers solutions-centric critical thinking for insightful, change-oriented results to continually contribute to the advancement of medicine. Ambitious Self-Starter who rises above industry, investixxxxxxtor-initiated, and RTOG and NCI clinical trial challenges to achieve winning outcomes, including quickly adapting to evolving, high-pressure scenarios with knowledge of cutting-edge techniques and pioneering medical breakthroughs. Excellent Communicator who develops synergistic relationships with key decision-makers, cross-geographical healthcare professionals, stakeholders, study participants, and the general public, and who leads peers by example and with ethics and integrity.

Clinical Research Coordinator

Capitalize on the opportunity to lead forward-thinking clinical research, including coordinating and managing 15+ active industry, investixxxxxxtor-initiated, and RTOG and NCI clinical trial protocols, as well as performing comprehensive internal audits to monitor compliance with guidelines and protocols. Demonstrate experience in radiation oncology research and various malignancies, including solid tumors (i.e. breast, prostate, head and neck), GI, and hematology. Coordinate all clinical site and / or study visits and procedures according to protocols. Develop case report forms and regulatory documents, as well as operational statistical reports rexxxxxxrding patient accrual and data compliance protocols. Lead team meetings and present reports to trial team / sponsors. Perform chart auditing for internal / external review. Report and document study drug adverse effects.

         Achieved zero major deviations from key audits.

         Led team training across several clinical study protocols.

         Increased study accrual through innovative subject recruitment.

         Developed new recruitment strategies, interviews, and questionnaires.

         Attained a flawless record of consistency for CRF and regulatory documents.

         Ensured compliance with protocols and conducted ongoing pre-audit team monitoring.

         Served as the primary liaison for pharmaceutical, study monitors, and IRB representatives.

         Seamlessly managed multiple research EDC databases, EMRs, data platforms, and Microsoft Office.

Program Coordinator ￨ Counselor

Strategically steered program-specific initiatives within this high-volume blood center, including developing and reorxxxxxxnizing recruitment and retention processes, conducting baseline interviews of study participants, and notifying and counseling donors with reactive markers for HIV, HBV, HCV, and HTLV. Exhibited skill in facilitating accurate qualitative and quantitative data analyses, and provided timely feedback and multi-site progress reports.

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Program Coordinator ￨ Counselor

         Increased overall enrollment and successful retention of study participants.

         Trained and mentored department staff on study protocols and implementation.

         Increased recruitment of eligible donors, and managed a risk factor study database.

         Coordinated NIH-funded Multicenter Case-Control Study (U.S. Donor Risk Factor Study).

Physician

Utilized broad scope of medical knowledge toward providing outpatient primary care of 50 patients daily within a community hospital setting, as well as inpatient care in internal medicine, surgery, and obstetrics and gynecology.

         Reduced hospital-wide infant and maternal mortality rates.

         Collaborated with midwives to improve adherence to delivery protocols.

         Improved public s contraceptive use via community enxxxxxxgement and reproductive health counseling.

Physician ￨ Quality Assurance Officer

Delivered excellence in outpatient clinical services for 40 patients daily, including managing proper care of patients by accurately monitoring treatment, billing, and follow-up processes. Developed, reviewed, and / or implemented results-generating corrective action plans, as well as detailed SOPs to maximize orxxxxxxnizational safety.

         Continually identified and evaluated critical risk areas related to accreditation.

         Managed a network of 20 healthcare facilities for a Health Maintenance Orxxxxxxnization.

Medical Intern

Played a vital role in providing superior care of 50 patients daily within fast-paced inpatient and outpatient settings, including comprehensively educating and orienting staff members on protocols to promote key safety.

         Enhanced community health via proactive outreach to underserved populations.

         Optimized staff and patient safety by creating process and performance improvement plans.

Master of Public Health

Bachelor of Medicine & Surgery

SPSS ￨ SAS ￨ TrialMaster ￨ Medidata (Rave) ￨ Varian Eclipse

EMR (PowerChart, EPIC) ￨ IDX ￨ InForm ￨ MRS (DataTrack) ￨ ARIA ￨ OnCore

Microsoft Office Professional Suite (Word, Excel, PowerPoint, Outlook, Access, Publisher)