Clinical Research Coordinator

BOLAJI OLADAPO

***** ********* **** ********, **. 77407

Phone: 281-***-****, E-mail: *******@*****.***

OBJECTIVE: To obtain a position in Clinical Research, where my educational background, clinical trials expertise, strong work ethics, and exceptional leadership skills will be best utilized to meet scientific research goals and business objectives.

THERAPEUTIC EXPERIENCE: Phases I, II, III, & IV.

CNS, Endocrinology, Infectious Disease, Cardiovascular, and Oncology

EDUCATION: Bachelors of Science in Micro-biology

Associate in Arts, (Liberal Arts-General Option)

Certificate in Venipuncture (Phlebotomy)

Diploma in Clinical Research

CPR and First Aid certified

RELEVANT SKILL: Comprehensive knowledge of ICH GCP, and IRB guidelines, as well as FDA

regulations

PROFESSIONAL

EXPERIENCE:

PHARMA CLINICAL SERVICES – Glenolden, Pa.

Clinical Research Coordinator, July 2007 to Present

• Monitor the conduct of clinical studies, as well as site compliance activities in adherence with GCP guidelines

• Schedule site initiation visits

• Responsible for ensuring the completion of regulatory documents and the shipment of study-related materials

• Schedule and oversee all subject visits on assigned protocols

• Monitor AEs & SAEs to ensure investigators’ proper compliance of events

• Assist the study manager in performing task related to protocol development

• Properly consent subjects in accordance with FDA, GCP and protocol guidelines

• Ensure the safety and welfare of all study subjects

• Collection, labeling, and organization of biological specimens when necessary

• Collect and accurately record study data in source documents and case report forms

• Monitor electronic CRF by using Datatrack System

• Conduct and document GCP audits of investigator sites to verify that clinical trials are conducted in compliance with FDA and protocol requirements

CLINTRIAD PHARMA SERVICES - Coatesville, Pa.

Clinical Trial Coordinator, December 2005 to July 2007

• Facilitate all site visits with monitors and sponsors

• Collected and reviewed regulatory documents

• Schedule and prioritize workloads to meet projected deadlines

• Assisted in ensuring that all site data queries were addressed in a timely fashion

• Ensured that all protocol conduct was within ICH-GCP guidelines

• Reviewed, maintained, and archived study administrative and data management files

• Coordinate and participate in protocol assessment and site preparation for study initiation

• Review of drug accountability records

SPECIAL PEOPLE IN NORTHEAST, INC. - Philadelphia, Pa.

Assistant Director, September 1999 to December 2005

• Monitored and evaluated patient care services

• Acted as the point of contact for resident and family concerns

• Ensured that the home was in compliance with state and federal regulations

• Developed and implemented policies and procedures

• Managed annual budget dealing with quality of care and staffing patterns

• Oversaw account receivables

• Assumed full responsibility of the home in the absence of the executive director

COMPUTER EXPERIENCE

• Word

• Outlook

• Excel

• PowerPoint

• Access

• EDC

• RDC

• Datatrack System

.

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