Bright Nyamekye
** **** ******* ***. 201-***-****
Clifton, New Jersey 07011 acux8y@r.postjobfree.com
Doctor of Medicine graduate with excellent Physician’s Assistant experience and Research education. Strong interest in participating in compensated or volunteer clinical research opportunities. Also interested in teaching and any other job position in the healthcare field. Excellent skills and education to successfully perform research in a hospital or pharmaceutical company. Strong academic credentials, excellent work experience and vast transferable skills obtained through 2 years of successful Physician’s Assistant work. Outstanding interpersonal and communication skills, superior accuracy in patient history charting and other documentation responsibilities.
Areas of Expertise
Doctor of Medicine Credentials
Physician’s Assistant Experience
Clinical Research Skills
Multiple Graduate Degrees
Chronic & Acute Care Patients
Diagnosis & Treatment
Nursing Home Patients
Hematologic Illness Patient Care
Cancer Patient Care
Bone Marrow Biopsies
Infusion Lab
Administering Chemotherapy
Computer skills: Microsoft office, word, excel and powerpoint.
Professional Experience
VINEYARD COLUMBUS CHURCH CLINICAL INTERNSHIP, OH MARCH 2016 – PRESENT
Effectively examined patients (without insurance) with acute and chronic illnesses, under the close supervision of the attending physician.
Visits patients in nursing homes, hospital and home visits providing medical treatments
Also help in the church food pantry in providing food to the homeless and poor
DR. GONZALES - VIRGINIA CLINICAL TRIAL, WARRENTON, VA OCT, 2015 – FEB, 19 2016
(Clinical Research Associates)
Assist in the ongoing scientific review of the clinical data and support trial data analysis, reporting and publishing.
Assist in the training of new staff
Contribute to the Outsourcing of specific clinical research project to a particular CRO.
Contribute to the development of protocol and manage simple clinical trial.
Intervene and manages SAE that may arise during clinical trial.
Other familiar document stored in the TMF includes the GCP training files, SAE (severe adverse effect) notices, master inform consent log or enrolment log, investigator brochure, contact list of CRA’s, safety reports, monitoring letters and site visit logs
DR. NAVEEN DOKI (CLINIC WITH INFUSION LAB)– HEMATOLOGY AND ONCOLOGY REASEARCH EXPERIENCE, FAIRFAX, VA JULY, 2013 TO JUNE. 2014
(Clinical Research Coordinator)
Assist in evaluating new protocols for feasibility at the site
Work closely with the research team to ensure the organization of various regulatory, clinical and non clinical documents. These includes complete and signed FDA 1572 forms, Financial disclosure form, Approved CV’s of staff listed in 1572 forms, Lab certificate with normal ranges, signed contract, IRB rosters and approval notices (which includes IRB approved letters, informed consent, protocol and amendments, advertisement and subject recruitment materials).
Other familiar document stored in the TMF includes the GCP training files, SAE (severe adverse effect) notices, master inform consent log or enrolment log, investigator brochure, contact list of CRA’s, safety reports, monitoring letters and site visit logs.
Familiar with the negotiation of contracts and budgets in clinical trial which involves negotiating for every line, procedure and visit.
Gain experience in study Initiation, Monitoring and Closing.
Clinically assisted in the blood withdrawal and drug dispensation to clinical subjects. This is then followed by reviewing patient chart for source documentation, case report form development, Lab values interpretation, severe adverse event intervention and signed informed consent.
Site identification which requires evidence based sources such as the electronic health information resources.
Recruitment strategy which involves working with the recruitment specialist for the site identification merchant proposal. Subjects enrollment usually involves using simulation, forecasting and contingency planning application.
PRACS INSTITUTE, FARGO, NORTH DAKOTA APRIL, 2012 TO MAY. 2013
(Clinical Research Assistant)
Assist in evaluating new protocols for feasibility at the site
Work closely with the research team to ensure the organization of various regulatory, clinical and non clinical documents. These includes complete and signed FDA 1572 forms, Financial disclosure form, Approved CV’s of staff listed in 1572 forms, Lab certificate with normal ranges, signed contract, IRB rosters and approval notices (which includes IRB approved letters, informed consent, protocol and amendments, advertisement and subject recruitment materials).
Other familiar document stored in the TMF includes the GCP training files, SAE (severe adverse effect) notices, master inform consent log or enrolment log, investigator brochure, contact list of CRA’s, safety reports, monitoring letters and site visit logs.
Familiar with the negotiation of contracts and budgets in clinical trial which involves negotiating for every line, procedure and visit.
Gain experience in study Initiation, Monitoring and Closing.
Clinically assisted in the blood withdrawal and drug dispensation to clinical subjects. This is then followed by reviewing patient chart for source documentation, case report form development, Lab values interpretation, severe adverse event intervention and signed informed consent.
Site identification which requires evidence based sources such as the electronic health information resources.
Recruitment strategy which involves working with the recruitment specialist for the site identification merchant proposal. Subjects enrollment usually involves using simulation, forecasting and contingency planning application.
PROFESSOR JORDAN (BIOCHEMISTRY) REASEARCH EXPERIENCE, RUTGERS UNIVERISTY, NJ JAN. 2007 TO DEC. 2007
(Research Assistant)
Worked as a research assistant in evaluating the activities of various respiratory enzymes.
Experience with mass spectrometry, dna and protein electropholysis, PCR and RFLP.
Have knowledge on various testing methods and perform all manual operations on various supplies.
Perform laboratory analysis on all materials after appropriate sterilization.
Perform various culture of micro organisms in isolation according to standard inhibition and ensure controls over moisture and temperature.
Knowledgeable in sciences including organic chemistry, microbiology, cell biology and biology.
METROHELATH HOSPITAL, CLEVELAND, OHIO JULY 2012 TO JUNE. 2013
MEDICAL RESIDENT
Work in consultation-liaison, inpatient psychiatry, emergency psychiatry and outpatient medicine
Consult and Liaison:
Managed patients with acute psychiatric and medical conditions within inpatient settings.
Helped the attending physician to diagnose treat and mediate patient transfer.
Helped determine whether a patient has the capacity to make medical decision.
Participated in the treatement of patient with acute agitations
Emergency Services:
Attended patients with acute psychotic patients in the emergency setting.
Help in the screening of patients in the emergency setting to determine admissions and discharges of patients
Aided and coordinated the transfer of patient from the ER to the inpatient and outpatient clinics
Inpatient psychiatry:
Helped in the management of patient transferred into the inpatient ward
Rounded with different attending in the morning and in the afternoon to manage and determine the status of various patients
Coordinated the various discharges of patients in the inpatient setting
Work closely with nurses as a team to ensure good patient care
Outpatient medicine:
Examined patients in need of chronic and acute care. With the supervision of the attending physician, diagnosed and treated patients’ illnesses.
Participated in various office procedures including skin tag removal, ear irrigation, wound care, pap smear and various biopsis.
Responded to various patient calls from outside and coordinated treatment if needed
Solomon Owusu, MD, JERSEY CITY, NJ NOV. 2014 TO MAY. 2015
Effectively examined both adult and pediatric patients with acute and chronic illnesses, under the close supervision of the attending physician.
Rafael Lucila, MD, Clifton, NJ Aug. 2014 to Sept. 2014
Physician’s Assistant
Examined patients in need of chronic and acute care. With the supervision of the attending physician, diagnosed and treated patients’ illnesses.
Assisted Physician in minor office procedure such as ear irrigation, cortisone shot, and skin tag removal
Riza Awan, MD, Newark, NJ June 2014 to July 2014
Physician’s Assistant
Effectively examined patients with acute and chronic illnesses, under the close supervision of the attending physician.
Visited patients in nursing homes and during home visits.
Carlos Gonzalez, MD, Fairfax, VA Nov. 2013 to April 2014
Physician’s Assistant
Managed the care of clinic patients with acute and chronic illnesses.
Naveen Doki, MD, Fairfax, VA Sept. 2013 to Oct. 2013
Physician’s Assistant
Managed patients with hematologic illnesses and cancer.
Helped the attending physician diagnose treat patients.
Participated in various procedures including bone marrow biopsies.
Worked in the infusion lab to administer chemotherapy and other medications.
Familiar with electronic healthcare record – EPIC for keeping patients medical records
Magnus Ikhinmwin, MD, Fairfax, VA July 2013 to Aug. 2013
Physician’s Assistant
Helped manage patients with acute and chronic illnesses under the close supervision of the attending physician.
INOVA FAIRFAX HOSPITAL, LEESBURG, VA AUG. 2015 TO SEP. 2015
I volunteer as a clinical technician that assist the nurses and the rest of the medical team in the daily management and treatment of patients at the hospital floor inpatient unit.
Education & Training
Graduate, Doctor of Medicine, Ross Medical School, Roseau, Commonwealth of Dominica
Graduate of Science Candidate, Clinical Research Administration, Grad. Dec. 2014, Walden University, Minneapolis, MN
Undergraduate, Rutgers University, Newark, NJ
Certificate, Protecting Human Research Participants, National Institute of Health, Bethesda, MD