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Clinical Research Medical

Location:
Gwynn Oak, Maryland, United States
Posted:
September 21, 2019

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Resume:

Feyi Akinduro

346-***-****

adaeqm@r.postjobfree.com

feyiyemia@gmail. com

https://youtu.be/Q1ct3tuTCwM

https://www.linkedin.com/in/feyi-akinduro-41783112a Skills

Organization

Coordination

Microsoft office

Analytical mindset

Commitment

Measuring Blood Pressure

Attention to details

Good Communication Skills in English,written and verbal Responsible

Phlebotomy

EKG

Experience

Clinical Research Fastrack August 2019

● ICH/GCP.

● Data Validation by using ALCOA-C.A-attributable by who when and what,L-legible and clear to leave space for correction,C-contemporaneous by recording date and time,O-original by making sure the data is original,A-accountable by checking the Units or measurement and C-by making sure that the data is complete.

● 21 CFR Part 11,21 CFR 50,21 CFR 54,21CFR56

● Data management .

● Informed consent form (ICF) and the Process of taking ICF.

● Monitoring Clinical trials from SIV to Close Out

● Reconciliation of Regulatory binder and CRF

● TMF

● Clinical trial Operations from Feasibility to close out.

● Following Good documentation practice (GDP).

● Following FDA regulations.

● Maintaining Regulatory Binder including the likes of 1572,trial logs,ICF, DOA etc

● Reading,Understanding and execution of Clinical Trial Protocol.

● Investigational product(IP) accountability.

● Query Resolution.

● Writing CAPA.

● Identification and reporting Adverse event and serious Adverse Event (AE&SAE) Clinical Research Coordinator

University of Medical Science Teaching Hospital,Akure Dec 2014 till Feb 2017. Recruited,enrolled and retention of sickle cell patients on using hydroxy urea to reduce crisis & recruited and enrolled patients with HIV on low Cd4 count to use Azithromycin prevention of tuberculosis in a known HIV patients.

● Adhered to IRB approved protocol.

● Data Validation by using ALCOA-C.A-attributable by who when and what,L-legible and clear to leave space for correction,C-contemporaneous by recording date and time,O-original by making sure the data is original,A-accountable by checking the Units or measurement and C-by making sure that the data is complete.

● Participated in the informed consent process of study subjects.

● 21 CFR Part 11,21 CFR 50,21CFR 54,21 CFR56

● Coordinated protocol related research procedures and follow up caregivers.

● Screened,recruited and enrolled patients.

● Maintained study source documentation.

● Entering subject data into EMR system.

● Ensured Quality documentation and accountable IP, Reconciled CRF and Regulatory binder.

● Reported adverse events (AE) and severe adverse events (SAE) within 24 hours.

● Understood good clinical practice (GCP) and regulatory compliance.

● Educated subjects and Family on protocol.

● Complied with Institutional policies,standard operating procedure (SOP) and guidelines.

● Collaborated with other departments i.e Laboratory,Pharmacy.

● Assisted the PI with financial aspects of the trial including budget & contracts. Medical Doctor

University of Medical Science Teaching Hospital,Akure Dec 2014 till Feb 2017

● Documented patient's histories like identifying data,chief complaints,illnesses,family histories.

● Managed Hematology Oncology cases and Emergency cases of Hematology and Virology.

● Diagnosed health conditions based on patient's symptoms,health histories,laboratory,diagnostic radiology test results or other physiological measurements such as EKG.

● Administered,dispensed,or prescribed medications.

● Participated in cross training to remain flexible and adaptable to patient's support demands. Chief Medical Doctor

National Youth Service Corps Camp Oka Akoko Oct 2014 till Dec 2014

● Managed the Clinical affairs of the Camp (population of about 2500 graduates ).

● Allocated Doctor,Nurses,Pharmacists and dentists to be on duty and supervised them.

● Made sure every patient that presented to the Clinic received proper and adequate treatment House Officer/Internship

Federal Medical Centre,Owo September 2013 - October 2014

● Interned in the Medical, Surgical, Pediatric and Obstetric & Gynecology Units.

● Provided care and stabilized patients pending consultant review. Medical Clinical Clerkship

University of Ife Teaching Hospital,Nigeria Jul 2012 till April 2013

● Obtained history from patient,documented the history,did physical examination,presented it to a consultant for review,and ordered for investigations. Education

● Clinical Research Fastrack /228 hours/ 2019

● CPR,AED & First Aid Certification 2018

● Registered Medical Assistant by Healthcare Professional Registry of United States 2018

● Crimea State Medical University 2006 - 2012

Reference

● Lauren Ballina Chang National Program Director clinical research Fastrack 724-***-****.

● David Silberman MPH 415-***-****.

● Olufemi Adejumo Clinical Research Professional 347-***-****.



Contact this candidate